key: cord-0788950-z8eh611w authors: Velappan, Nileena; Close, Devin; Hung, Li-Wei; Naranjo, Leslie; Hemez, Colin; DeVore, Natasha; McCullough, Donna K; Lillo, Antonietta M; Waldo, Geoffrey S; Bradbury, Andrew R M title: Construction, characterization and crystal structure of a fluorescent single-chain Fv chimera date: 2021-02-15 journal: Protein Eng Des Sel DOI: 10.1093/protein/gzaa029 sha: 486a00d394f1d2bb5420d8659e743295a0696d82 doc_id: 788950 cord_uid: z8eh611w In vitro display technologies based on phage and yeast have a successful history of selecting single-chain variable fragment (scFv) antibodies against various targets. However, single-chain antibodies are often unstable and poorly expressed in Escherichia coli. Here, we explore the feasibility of converting scFv antibodies to an intrinsically fluorescent format by inserting the monomeric, stable fluorescent protein named thermal green, between the light- and heavy-chain variable regions. Our results show that the scTGP format maintains the affinity and specificity of the antibodies, improves expression levels, allows one-step fluorescent assay for detection of binding and is a suitable reagent for epitope binning. We also report the crystal structure of an scTGP construct that recognizes phosphorylated tyrosine on FcεR1 receptor of the allergy pathway. Fluorescently labeled antibodies are extensively used in diagnostic and research methods such as immunofluorescent microscopy and flow cytometry. The latter allows the rapid and quantitative analysis of single cells within a large population, and fluorescent-activated cell sorting (FACS) allows the sorting of individual cells based on their specific fluorescent patterns. Antibodies used in these assays are typically labeled with fluorescent chemical compounds. For example, a succinimidyl ester functional group attached to a fluorophore core may react with primary amines to label the antibody. However, this strategy may reduce or eliminate binding if there are primary amines within the antigen recognition regions (Mccormack et al., 1996) . Different antibodies react with different fluorophores at different rates, creating variability in experimental settings. Furthermore, since the labeling is stochastic, some antibodies will have large numbers of fluorophores and some very few. Fluorophore over-conjugation can result in quenching and dimmer antibody molecules than those with less fluorophore conjugation (Haugland, 1995) . While standard techniques have been developed to perform antibody labeling reactions, batch-to-batch variation and labeling can also affect antibodyantigen recognition (Vira et al., 2010) . One of the most effective methods to develop antibodies is to select them from large combinatorial libraries using phage and/or yeast in vitro display technologies (Boder and Wittrup, 1997; Ferrara et al., 2012; Marks et al., 1991; Sblattero and Bradbury, 2000) . As full-length antibodies cannot be directly displayed easily, Fabs or single-chain variable fragments (scFvs) (Huston et al., 1988) , which comprise the antibody heavy-chain variable (VH)-and light-chain variable (VL)-binding domains, can be displayed on phage or yeast fused to surface display proteins. The scFv genes can be constructed by connecting VH and VL regions with an unstructured linker peptide (Huston et al., 1988) , or one that comprises a translated DNA recombination signal (Sblattero and Bradbury, 2000) . The genes encoding the variable regions are available during the selection process and can be reformatted into many different functional modalities (Bradbury and Pluckthun, 2015) . However, scFvs tend to aggregate, have low expression levels and are unstable during long-term storage (Arndt et al., 1998) . To monitor binding, scFvs are typically tagged, then detected using an anti-tag antibody and appropriately labeled secondary antibodies. Several strategies have been used to overcome these limitations ( Fig. 1) , including cloning as full-length antibodies (Persic et al., 1997) or scFv-Fc fusions (Shu et al., 1993) , in which case traditional labeled secondary antibodies can be used. Fusion to enzymatic or fluorescent proteins allows detection without the need for secondary antibodies. The scFv-alkaline phosphatase (AP) fusions (Lindner et al., 1997) are stable and functional, allowing single step detection of bound antibody. Fusion of green fluorescent protein (GFP) or other fluorescent proteins (FPs) to the C terminus of scFv genes yields intrinsically fluorescent scFv. However, scFv-GFP fusions tend to be poorly expressed (Casey et al., 2000) . The scFv folds best in oxidizing environments, such as the bacterial periplasm or eukaryotic secretory pathway (Kipriyanov et al., 1997) , while most FPs are best expressed in the reducing environment of the cytoplasm. A notable exception is superfolder GFP (Pédelacq et al., 2006) . This expression incompatibility has been overcome by fusing a short tag derived from split GFP to the C terminus of the scFv (Ferrara et al., 2011) and carrying out the complementation in vitro, fusing GFP to particularly stable scFvs (Nizak et al., 2003) , or creating nanobody FP fusions (Rothbauer et al., 2008) . Markiv et al. (2011a,b) described an alternative concept to generate fluorescent scFvs in which the FP was placed between the VH and VL as a linker (VH-FP-VL) and could be expressed in the bacterial cytoplasm. The fluorescent proteins used included mRFP1 (derived from DsRed), BFP, mCerulean and mCitrine to produce red, blue, green and yellow antibodies. The alternative orientation, VL-VH, was not attempted. Chain orientation may be important in binding properties, and the strategy described in that publication may not be compatible for scFv libraries constructed in the VL-linker-VH orientation. Markiv et al. (2011a,b) use the term REDantibody in their first description of the technology. However, no specific terminology was used in the subsequent paper when additional fluorescent proteins were tested (Markiv et al., 2011a,b) . Here we refer to the concept of fluorescent antibodies created using a fluorescent protein as a linker as single-chain fluorescent protein (scFP), with specific formats called out for individual scFPs, e.g. scTGP for the scFPs described here in which the thermal green protein (TGP) (Close et al., 2015) is used as a linker. Figure 1 provides a visual summary of exemplar scFv modifications utilized in research in comparison to the scTGP format presented here. TGP is an extremely stable, highly soluble, non-aggregating green fluorescent protein that was engineered in our lab (Close et al., 2015) to overcome the problems of solubility and aggregation with many traditional GFPs and their variants. TGP was engineered by disrupting crystal lattice contacts and introducing high-entropy glutamate residues to improve crystallization and prevent oligomerization. The monomeric nature of TGP makes it potentially suitable for insertion into scFv genes, substituting the linker originally used to tether the VL and VH. In this study, we construct single-chain fluorescent proteins (scFPs) as VL-TGP-VH. These scFPs are fluorescent, are functional in yeast display technologies and are expressed at high levels in the bacterial cytoplasm. We describe the construction of scFPs and their functionality using multiple assays. We use three scFvs and compare them with the corresponding scTGP formats. The antibodies p1-1 and p13B1 recognize phosphorylated immunoreceptor tyrosinebased activation motif (ITAM) peptides of FcεR1 receptor of the allergy pathway (Velappan et al., 2019) and the anti-tyrosine sulfate antibody recognizes the post-translationally modified tyrosine within proteins or peptides (Kehoe et al., 2006) . We report the X-ray crystal structure of scTGP p1-1. Finally, we use scTGP and IgGs to develop a novel epitope binning method for multimeric proteins. We demonstrate this method using three antibodies against Yersinia pestis, the causative agent of plague (Lillo et al., 2011; Lillo et al., 2020) . Epitope binning uses competitive pairwise binding assays to sort antibodies into bins recognizing the same or different epitopes. Antibodies binned together often have similar functional activity (e.g. block binding to a cell surface receptor), while those in different bins recognize different epitopes and consequently may have different functional activities. This proof of concept demonstrates the utility of the scTGP format for generating clinically relevant antigen detection tools. The scTGP constructs were prepared using inverse PCR and circular polymerase extension cloning (CPEC) assembly. The vector was amplified using scFv linker-specific primers DCO 111 (TCCT-CAAGCGGTACCCAGGTGCA) and DCO 112 (TCTGGAGGGTC-GACCATAACTTCG). This primer combination was used to amplify the yeast display vector as well as the bacterial expression plasmids containing the scFv gene(s). The TGP gene was amplified using DCO 109 (TCTGGAGGGTCGACCATAACTTCGGTAATTAAAC-CGGAAATGAAAATTAAATTGCG) and DCO 110 (TATTCTG-GCGGAGGCAGCGGATCCTCAAGCGGTACCCAGGTACA). Q5 polymerase (M4091, New England Biolabs) was used for all amplification reactions according to manufacturer's instructions. Both vector and insert were gel purified prior to CPEC assembly. CPEC assembly was performed by combining equimolar amounts of vector and fluorescent protein insert and reducing the annealing temperature gradually from 70 to 55 • C using 10 s intervals. Upon completion of the CPEC assembly, the reaction was purified using a mini-elute column (28004, Qiagen Inc.). The constructs were eluted into 10 μl of 1:2 elution buffer: water and transformed via electroporation to bacterial cells. Yeast display constructs were transformed into Omnimax T1 or TOPO 10 cells (C854003 or C4044003, ThermoFisher Scientific) according to manufacturer's instructions and bacterial expression plasmids were cloned into BL21 DE3 (archival samples LANL) cells. Constructs were verified by DNA sequencing after cloning. Yeast display plasmids (based on pDNL6) (Ferrara et al., 2012) were transformed into Saccharomyces cerevisiae EBY100 and cloned by gap repair using the Yeast1 kit (Sigma Inc.). In this vector system, the scFvs are fused to the C terminus of the AGA2 protein of the yeast for surface display and the SV5 peptide tag is used to assess display levels on yeast. The transformed yeast were grown in SD/CAA (5 g/l casamino acids (−ade, −urs, −trp), 20 g/l dextrose, 1.7 g/l yeast nitrogen base, 5.3 g/l ammonium sulfate, 10.19 g/l Na 2 HPO 4 .7H 2 O and 8.58 g/l NaH 2 PO 4 ) agar plates at 30 • C for 2 days. Single colonies were further grown in SD/CAA liquid culture at 30 • C until the culture reached an OD 600 of >2. 1/10th volume of this culture was added to SG/R CAA media (same as selective media except substitute the following sugars for dextrose: 20 g/l galactose, 20 g/l raffinose, 1 g/l dextrose) and induced at 20 • C as described previously (Ferrara et al., 2012) . Yeast inductions were allowed to proceed for 2 days to further improve display of scTGP. After induction, yeast cells were incubated with phycoerythrin (PE) conjugated anti-SV5 IgG (1 μg/ml) to assess scFv/scTGP display levels. In the case of scTGPs, the display levels were also assessed using the fluorescence at 530 nm when excited using 488 nm laser. The time course experiment reported in Supplementary Fig. S1 , available at PEDS online, was performed with three different colonies of yeast from each of constructs. For analysis on three consecutive days post-induction, 100 μl of yeast was taken, fluorescence of yeast was analyzed using flow cytometry and average fluorescence along with standard deviation from these replicates was calculated. Antibody p1-1 (Velappan et al., 2019) recognizes a 25 amino acid peptide that corresponds to the ITAM region of the FcεR1 receptor of mast cells when the first tyrosine of this peptide is phosphorylated, and peptide was named p1 (KVPDDRLYEELHVYSPIYSALEDTR, the phosphorylated tyrosine is bold and underlined). Antibody p13B1 (Velappan et al., 2019) recognizes the same peptide when all three tyrosines are phosphorylated and designated as p123 (KVPDDRLYEELHVYSPIYSALEDTR). The M2 peptide of influenza A was used as non-specific antigen (MSLLTEVET-PIRNEWGCRCNDSSD). The yeast (100-200 μl) were first washed with yeast wash buffer (YWB-30 mM Tris pH 8.0 with 0.5% BSA), by centrifugation at 13 000g. The binding assays were performed using 100 nM peptide antigens diluted in YWB and incubated for 1 h at room temperature with rotation. Unbound peptide was washed away using YWB. The antigen bound yeast was further stained with anti-SV5 PE (1 μg/ml) and streptavidin labeled with Alexa 633 (S21375, ThermoFisher Scientific, 5 μg/ml) for biotinylated peptide detection. Washes with YWB were conducted to improve specificity of binding. All incubations and washes were performed at room temperature. The yeast display analysis was performed using FACS Aria and/or LSR II cytometers (Becton Dickinson). For each flow cytometry analysis, 10 000 events were collected and average value was used to report mean fluorescence intensity (MFI) for display level and binding signal and the assays were repeated multiple times to ensure accuracy. Experiments were performed in triplicates to measure the K d values. Affinity measurements were conducted by serial dilution of the biotinylated peptide antigens as described previously (Ferrara et al., 2012; Velappan et al., 2019) . K d determination was performed using GraphPad Prism ® software using the equation for one site-specific binding, which uses non-linear regression analysis to fit the curve. All genes were cloned into the vector systems described below, using restriction enzymes BssH II and Nhe I (R0199 and R3131, New England Biolabs). The scFv and scTGP genes were both cloned into pEP, a periplasmic expression vector, while the scTGP constructs were also cloned into pETCK3, a cytoplasmic expression system. The protein expression in both plasmid systems is controlled by the T7 promoter system. To produce scFvs and scTGPs, bacterial colonies were streaked on LB kan/glu (kanamycin 50 μg/ml and glucose 3%) plates and incubated at 37 • C overnight. A second overnight culture was grown in 1-10 ml of LB media containing kanamycin and glucose. Liquid culture was grown at 30 • C. The overnight culture volume was set to 1/10th final expression culture volume. The following day, the overnight culture was diluted to half the final culture volume and grown in kan/glu media at 30 • C for 2 h. The culture was centrifuged (6000g for 6 min) and the pellet was re-suspended in auto-induction (AI) media containing kanamycin (Studier, 2005) . AI media allows protein induction without the use of isopropyl β-d-1thiogalactopyranoside (IPTG). Here, glucose, glycerol and lactose are added to buffered yeast broth growth media. As the Escherichia coli cultures grow, they consume glucose first. As the glucose depletes, the bacteria are forced to utilize lactose inducing the T7 promoter and allowing protein production. The culture was incubated at 30 • C for 4 h. Subsequently, the temperature was reduced to 18 • C and protein expression continued for 2 days (scFvs) or up to 3 days (scTGPs). The cell culture was spun down (10 000g, 20 min) and frozen prior to protein purification. Three colonies from each of the constructs (scFv-pEP, scTGP-pEP, scTGP-pET) for antibodies p1-1 and p13B1 were used to analyze functionality of proteins expressed in different bacterial compartments. About 1 ml of expressed culture was spun down and the bacterial pellet was lysed using 1/10 POP culture reagent (71092, EMD Millipore). Incubation time was 30 minutes at room temperature and the insoluble fraction was separated by centrifugation (20 000g at 4 • C). About 100 μl of cell culture was used to measure the fluorescence of pre-lysed culture and 100 μl of POP culture supernatant was used to measure fluorescence post-lysis. The cytoplasmically expressed scTGP had higher fluorescence than the periplasmically expressed scTGP. Fluorescence-linked immunosorbent assay (FLISA) was performed with two normalizations: equal volume or equal fluorescence. Here, 100 μl of post-lysis supernatants or volume of supernatants adjusted to provide equal fluorescence was used. Both expression and binding assays were performed in triplicate and average values and standard deviations were calculated. A twotailed T-test was used to compare the two expression systems. The bacterial pellets were re-suspended in TNG buffer (50 mM Tris pH 8.0, 150 mM NaCl, 10% v/v glycerol) containing DNase 1 (PI89836, Thermo Fisher Scientific) and EDTA-free protease inhibitor tablet (11873580001, Roche Inc.). Cell lysis was achieved using a cell homogenizer (Avestin Inc.). The lysate was spun at 13 000g and the supernatant was then spun at 38 000g and filter sterilized to remove cell debris. Protein purification was performed using Ni-NTA agarose beads. The His-tagged proteins were allowed to bind to the beads for 1 h at 4 • C with rotation. The beads were washed with 5-10× volume of TNG buffer and TNG buffer containing 20 mM imidazole. Proteins were eluted with TNG buffer containing 250 mM imidazole. The protein was cleaved from the His-tag with TEV protease using 0.5-1 mg of TEV protease and the digestion proceeded in a dialysis cassette in TEV buffer (20 mM Tris [pH 8.0], 100 mM NaCl, 0.5 mM EDTA, 3 mM reduced glutathione) at RT, overnight. The His-tag fragment and any uncleaved protein were subsequently removed by a second pass through fresh Ni-NTA agarose beads. Protein concentration and purity were determined using protein electrophoresis and Coomassie staining, absorbance at 280 nm or using fluorescence intensity. Prior to crystallization, scTGP proteins were further subjected to chromatography on a 320 ml XK 26/60 Sephadex 200 size-exclusion column using an AKTA prime liquid chromatography system (GE healthcare). Fluorescent protein fractions were collected and assessed using gel electrophoresis and Coomassie staining for purity. Pure fractions were combined and concentrated using Amicon centrifugal filters with 30 kDa cutoff. Protein expression for these constructs was conducted multiple times during the course of the project to ensure consistency once the protocol was established. A typical protein expression volume was 1 L followed by FPLC purification. Neutravidin-(31000, Thermo Fisher Scientific) coated wells (100 μl of 10 μg/mL in PBS) were used in both enzyme-linked immunosorbent assay (ELISA) and FLISA (Velappan et al., 2008) to bind biotinylated antigens. Nunc maxisorp plates (12-565-136, ThermoFisher Scientific) and black maxisorp plates (43711, Nunc) were used for FLISA. The peptide antigens were synthesized with biotin at the N terminus and protein antigens were biotinylated using EZ-Link NHS-LC-LC-biotin (21343, Thermo Fisher Scientific) according to manufacturer's protocols. The wells were washed with PBS and blocked with blocking agent containing 2% milk (ELISA) or 2% BSA (FLISA) for 30 mM TRIS pH 8.0 was used as the buffer instead of PBS in binding assays with ITAM peptides. About 1 μg of bioantigen in 100 μl was added to blocked wells and was allowed to bind to neutravidin for 15 min while shaking. Excess antigen was washed off and equal amounts of scFv and scTGP antibodies were added in blocking buffer diluted to 10% in PBS. Antigen-antibody interactions were allowed to proceed for 1.5 h and excess antibody was washed with PBST (1× PBS, 0.1% tween) three times followed by three washes with 1× PBS. For ELISA, anti-SV5 antibody conjugated to horse radish peroxidase (HRP) was used as secondary reagent. The bound HRP was detected using its substrate TMB (T8665, Sigma Inc.) and the absorbance at 450 nm was read after quenching with 1 M H 2 SO 4 . For FLISA, fluorescence was directly measured after washing with excitation set at 488 nm and emission set to 530 nm. All binding assays were performed in triplicate and average values and standard deviation were calculated. We repeated the binding assay for p1-1 and p13B1 scFv and scTGP proteins at equimolar concentration (50 nM of antibody). The assay was performed as described above. The scTGP p1-1 was crystallized using the sitting drop vapor diffusion method. Protein (10 mg/ml) and reservoir solutions of 0.1 μl each were mixed and equilibrated against 30 μl reservoir at 298 K using a PHOENIX crystallization robot (Art Robbins Instruments). A set of crystallization reagents consisting of Crystal Screens, PEG/Ion screens (Hampton Research), PACT suite (Qiagen), and JCSG core suites (Qiagen) was used to screen for the propensity of crystallization. Subsequent grid screens to optimize buffer pH, concentrations of salt and precipitants, and additive screens were employed as needed until diffraction-quality crystals were obtained. Crystals of scTGP were harvested with CryoLoops (Hampton Research) and flashcooled in liquid nitrogen prior to diffraction experiments. Glycerol was added to the mother liquor as cryo-protectants to final concentrations of 5-20% for conditions that were not cryo-ready. X-Ray diffraction experiments were conducted at the 5.0.2 beam line at the Advanced Light Source at the Lawrence Berkeley National Laboratory. The crystal structure of scTGP was determined with the molecular replacement (MR) method using the PHASER program (Mccoy et al., 2007) in the PHENIX suite (Liebschner et al., 2019) . The TGP structure (PDB ID: 4TZA) (Close et al., 2015) was used as a search model to locate the TGP moiety of the scTGP. The rest of the protein chain was modeled with the AutoBuild (Terwilliger et al., 2008) program in Phenix. Manual model rebuilding and refinement was conducted iteratively until convergence with Coot (Emsley et al., 2010) and phenix.refine (Afonine et al., 2012) , respectively. The anti-F1 scTGPs were constructed by PCR from scFvs (YP 1, 2, 3, 4, 6, 8) (Lillo et al., 2011) as described above and cloned into the pETCK3 protein expression vector for expression in BL21 E.coli. Protein expression, purification, quantification and binding to specific antigen (biotin-F1V) and control antigen (biotin-myoglobin) were performed with FLISA as described above. FLISA with gradient protein concentration (2×) starting at 20 000 ng in 100 μl volume/well was used to determine the binding curve of scTGP YP2, YP3 and YP8 (these antibodies were determined to be the most functional antibodies in this suite). The corresponding anti-YP IgGs were synthesized at ATUM Inc. and the F1V recognition by these IgGs was evaluated by ELISA using anti-human HRP (97165, Abcam) as the secondary antibody . The epitope binning assay was performed similarly to FLISA. Here, the biotinylated F1V protein was bound to neutravidin-coated black immunosorp plates (8 wells/sample) and scTGP (5000 ng) was added to all wells. The binding proceeded for 30 minutes without washing while the titrations of the IgGs were performed. IgG concentrations ranging The table compares amount of protein displayed by the yeast, recognition signal for the specific peptide antigen, non-specific interaction signals and affinity of binding by two antibodies (p1-1 and p13B1) in both scFv and scTGP formats from 0.75-50 μg were used. One well contained scTGP only. The titrated IgG solutions were added to the wells and incubated for 30-60 min. The unbound molecules were washed using PBST/PBS and the fluorescence of the bound scTGPs was measured using a spectrophotometer with excitation at 488 nm and emission at 530 nm. A decrease in fluorescence or lack thereof was used to determine presence or absence of different epitopes. Duplicate assays were performed to calculate average values and standard deviation was used to determine error bars. Three scFvs were used to test TGP in the scFP construct in the VL-VH orientation: p1-1 and p13B1 are two antibodies previously selected against different phosphorylation states of the cytoplasmic domain of the Fc-epsilon receptor (Velappan et al., 2019) , and αTyrS is an antibody that recognizes the sulfotyrosine post-translational modification, independently of sequence context (Kehoe et al., 2006) . Figure 2 and Table I together show that p1-1 scTGP and p13B1 scTGP were displayed on the yeast surface and recognized their cognate peptide antigens. Figure 2 shows flow cytometry analysis of protein display and antigen recognition by p1-1 and p13B1 in scFv and scTGP formats. Table I shows mean fluorescent intensity (MFI) values for dot blots and includes comparison with control antigens. The display levels for the scFv or scTGP were measured using labeled anti-SV5 IgG (Hanke et al., 1992) , an antibody recognizing a peptide tag (SV5) at the C terminus. Data presented in Supplementary Fig. S1 , available at PEDS online, shows that 2 days of induction is more suitable for scTGP display. The display levels for scTGP formats were reduced by 50-80% compared to the smaller scFv protein format. As expected, the antigen recognition signal was correspondingly reduced. The specific peptide recognition for scTGP p1-1 was about 5% of the recognition signal of the scFv. The pattern was similar for the p13B1 antibody as well and showed nearly 50% reduction in display level and associated drop in signal for antigen recognition. The affinity measurements for scFv and scTGP antibodies showed that despite the reduction in recognition signal the calculated K d values were similar (within 4-fold) between the formats for a given antigen. The scFvs are commonly expressed in the periplasmic space of the bacterial cell, since this provides the oxidizing environment required (Kipriyanov et al., 1997) . However, higher levels of recombinant protein expression are usually observed in the E. coli cytoplasm. Therefore, we evaluated both compartments for scTGP protein expression using two different protein expression vectors. As shown in Fig. 3A and B, the cytoplasmic expression system (pETCK3) produced a statistically significant higher amounts of fluorescent protein in the soluble fraction after lysis compared to the periplasmic expression system. Furthermore, scTGP constructs expressed in the cytoplasm were more functional than those expressed in the periplasm, as assessed by the specific binding activity of the two formats (Fig. 3C) . The recognition signal for specific antigen is more than three times higher than the signal for control antigen. Based on these results, further bacterial expression was carried out in the E. coli cytoplasm using the pETCK3 vector system. Three scFvs and corresponding scTGPs were used in protein purification and functionality studies. All six protein variants were expressed in 1 l culture volumes, purified using Ni-NTA agarose beads (see methods) in parallel and eluted using identical volumes. Eluates were run on a protein gel to compare relative protein production levels. The Coomassie staining of the protein gel showed scFv and scTGP protein yield was comparable in the case of the p1-1 and p13B1 antibodies. The scTGP format significantly improved soluble yield of the αTyrS antibody (Fig. 4A) , consistent with relative total protein quantification (Table II) . The relative amount of protein degradation appears to be similar between the scFv and its respective scTGP construct. The functionality of both antibody formats (scFv and scTGP) was assessed using ELISA against specific and non-specific antigens (Fig. 4B ) using equal concentrations of the corresponding scFvs and scTGPs. ITAM peptides p123 and p1 were used as specific antigens for scFv/scTGP p13B1 and p1-1, respectively. Fibrinogen was used as the specific antigen for the anti-tyrosine sulfate antibody (Kehoe et al., 2006) . The p0 ITAM peptide and all non-cognate targets provide negative controls. The results showed that both the scFv and Fig. 2 Yeast display-based analysis of scFv and scTGP constructs for display level and recognition of specific antigen. The scFv and scTGP versions of two antibodies, p1-1 and p13B1, were cloned into the pDNL6 yeast display vector and protein display induced. Protein display levels were assayed using PE conjugated anti-SV5 antibody in panel A. In panel B, binding of scTGPs to their corresponding targets using the green fluorescence (FITC-A) of the TGP as a detection modality (instead of SV5) is shown in the x-axis. The y-axis shows the recognition of the biotinylated peptide bound to streptavidin Alexa 633. In the case of the displayed scFvs target binding is shown, but no display as measured by TGP fluorescence. p1-1 4.3 6.9 p13B1 5.5 6.9 αTyrS 0.7 6.0 scTGP format of the antibodies were functional and recognized the expected specific antigen with comparable recognition signals and the recognition signal for specific antigen is more than three times higher than signal for control antigen. The specificity of the scTGP antibodies were further investigated using a FLISA (Velappan et al., 2008) . The results showed that recognition of binding by scTGP can be assayed using fluorescence and all three antibodies showed specific recognition of their target antigen (Fig. 4C ). Data presented in Supplementary Fig. S2 , available at PEDS online, show that at equimolar concentration scFv and scTGP formats of p1-1 and p13B1 provide equivalent binding signals. Previous attempts to crystallize the p1-1 scFv were unsuccessful and we hypothesized that incorporation into the scFP format would promote crystallization. Large (>300 μm), green-colored rod-shaped crystals of scTGP p1-1 were observed in several conditions in the initial screening trials but did not diffract beyond 4 Å. Later, bipyramid-shaped crystals of scTGP p1-1 formed with 1.6 M citric acid pH 6.2 as crystallization buffer after 2 months. These crystals diffracted to better than 2.5 Å resolution and belonged to the P4 1 2 1 2 space group with cell dimensions of a = b = 130.96 Å, c = 122.74 Å. The complete data set has an R merge of 5.9% for the resolution range of 50-2.5 Å. Cell content analysis gave a Matthews coefficient of 3.17 Å 3 Da −1 and a solvent content of 61% with one copy of scTGP p1-1 molecule in the asymmetric unit. The final R work and R free values were 16.3% and 21.1%, respectively. The refined structure contains 1 scTGP p1-1, 2 glycerols, and 136 water molecules. Detailed data collection and refinement statistics are listed in Table III . The atomic coordinates and structure factors are available in the RCSB Protein Data Bank under accession code 6WZN. Figure 5 shows the crystal structure of scTGP p1-1, which revealed a single-chain protein with three distinct domains, the TGP domain (residues 119-335) and the scFv VL (residues 1-112) and VH (residues 346-465) domains. The linker residues 113-118 formed a short α-helix between the scFv VL domain and the N-terminal of TGP. Residues 336-345 linking the C-terminal of TGP to the scFv VH domain have relatively poor electron densities indicating partial disorder. Two glycine residues (338-339) in this linker were not modeled. The TGP structure was used as the MR search model and as the initial structure of the TGP domain in scTGP p1-1 structural refinement. When superposed together, the Cα root-mean-square deviations (RMSD) between the refined TGP domain (this work) and the four individual protomers in the TGP structure range from 0.24 to 0.41 Å. As expected, several FP structures such as PDB IDs: 4PPL, 5EBJ, 2GX2 have RMSDs within this range when superposed with the TGP domain of scTGP p1-1. This is consistent with the well-conserved sequence of these proteins (>90% identity) in this FP family. The structures of the VH and VL domains of this scTGP are also well conserved with structures in the Fab structure family such as PDB IDs: 1RZG and 3UX9. The superposed Cα RMSDs are about 0.5 Å between the VL domain of scTGP and similar light-chain structures and are 0.6-0.7 Å between heavy-chain structures. Cysteines 367 and 441 in the VH domain are in close proximity to each other. They did not form a disulfide bond as most of the corresponding cysteine pairs did in similar structures listed in Supplementary Table S1, available at PEDS online, except the VH domain of PDB ID: 4NIK (Robin et al., Fig. 3 Assessing protein expression systems for scTGPs. The scFv format of the antibodies is expressed in the periplasmic protein expression vector, pEP. The scTGP (scFP) format of the constructs was expressed in both pEP (periplasmic expression) and pETCK3 (cytoplasmic expression). Panel A shows the fluorescence obtained after protein expression in both vector systems using the corresponding scFv constructs as controls. The upper panel B shows fluorescence from 100 μl of cell culture after two nights of protein expression (pre-lysis). The lower panel B shows fluorescence for equal volume of POP culture supernatant (postlysis). The error bars were generated from three independent protein expressions. Panel C shows the functionality of scTGPs produced in the periplasmic and cytoplasmic compartments. Two scTGPs (p1-1 and p13B1) were analyzed by FLISA for binding to their cognate antigen (ITAM p13 peptide) using M2 peptide of influenza A as negative control. The activity of the scTGPs produced in the cytoplasm (green) was normalized to the activity of scTGP produced in the periplasm (orange) in two different ways: equal volume (light green) or equal fluorescence (dark green). * denotes a p value ≤ to 0.05. The error bars represent standard deviation generated from three independent binding assays. 2014). This could be attributed to, in part, the reducing environment provided in protein purification processes. We show that scTGPs could be successfully used for epitope binning of antibodies recognizing the recombinant chimeric Y. pestis F1V protein (causative agent of plague). Here, the effect of unlabeled IgGs on scTGPs binding was used to determine whether the two antibody formats bind to same or different epitopes, in a one-step assay (Fig. 6A ). An scTGP-F1V binding curve (Fig. 6B ) was used to estimate the half-saturating concentration of scTGP, optimal for detection of scTGP displacement. Figure 6C and D each show the results of competitive epitope binning assay for anti-F1V antibodies YP2, YP3 and YP8. Binding of scTGP was detected by fluorescence in the presence of non-fluorescent IgGs. Results suggest that antibody YP2 has a different epitope than YP3 and YP8 (Fig. 6C) , since no displacement of scTGP YP2 (i.e. lowering of fluorescence) is observed in the presence of IgG YP3 and IgG YP8. As expected, IgG YP2 displaced the scTGP YP2. The data also show that YP3 and YP8 antibodies compete for the same epitope, as displacement of scTGP YP8 was observed in the presence of IgG YP8 and IgG YP3 (Fig. 6D) . These results were confirmed by ELISA and flow cytometry experiments . A major problem with the use of antibodies in research and diagnostics has been their inconsistency, particularly lot-to-lot variation in polyclonals (Bradbury and Pluckthun, 2015; Schumacher and Seitz, 2016; Slaastad et al., 2011; Weller, 2016) . However, monoclonals have also been found to be problematic (Vaezi et al., 2014) , in some cases due to the expression of additional chains in hybridomas (Bradbury et al., 2018) , reflecting the uncharacterized nature of most commercial antibodies, including monoclonals (Bradbury et al., 2018) . In contrast to polyclonal antibodies from animal immunization campaigns, recombinant antibodies are expressed from defined plasmids where the sequences of the VH and VL genes are known. Recombinant antibodies can be obtained from hybridomas by cloning the VH and VL genes (Bradbury et al., 2018; Ruberti et al., 1994) , Fig. 4 Protein purification and functionality assays. Panel A shows scFv and scTGP proteins purified using Nickel NTA 6× HIS tag from a 1-l culture volume. The scFvs run slightly above 25 kDa, while scTGP run at ∼50 kDa. Panel B shows a comparison of the functionality of scFv and scTGP by ELISA. Panel C shows that only scTGPs are functional in FLISA assays. Data for three different antibodies (p13B1, p1-1, αTyrS) with binding profiles against four different antigens (one specific, and three non-specific-ITAM peptides p0, p123, p1 and fibrinogen) are shown. The ELISA/FLISA assays were performed in triplicate and error bars refer to standard deviation. as well by selecting from large combinatorial antibody libraries displayed on phage and/or yeast Marks et al., 1991) . Finally, scFv can be converted into full IgGs identical to animal-derived antibodies. A significant advantage to using display technologies to select antibodies is that the genes encoding the VH and VL genes are obtained concurrently with selection of the Fig. 6 Epitope mapping using scTGPs. The rationale behind epitope binning using scTGPs and IgGs is depicted in panel A. Here, the scTGP (green star) is allowed to bind to a dimeric protein. Upon addition of unlabeled IgG (red oval) scTGP is either displaced (lowering the amount of fluorescence) or remains the same (unchanged fluorescence). These two scenarios indicate IgG competition for the same epitope or IgG recognition of a different epitope, respectively. Panel B shows an example of a scTGP-F1V binding curve that was used to determine suitable non-saturating amount of scTGP needed for the epitope binning assay (in this case 5000 ng). Panel C and D show scTGP binding (fluorescence) in the presence of increasing concentrations of IgG (0-50 μg). The dots represent average fluorescence values with corresponding standard deviations (error bars). Panel C shows the displacement of the scTGP 2 by IgGs YP2 and lack of displacement by YP3 and YP8. Panel D shows the displacement of scTGP 8 by IgGs YP3 and YP8. For panels B, C, D two per moving average trend line is given as solid line and the line is extended to last value using dotted line. antibody specificity, making the generation of potentially useful derivatives relatively straightforward. Apart from reformatting as full-length IgGs (Persic et al., 1997) , VH and VL genes can be transformed into dimerizing (De Kruif and Logtenberg, 1996) or multimerizing (Dübel et al., 1995; Hudson and Kortt, 1999) antibody fragments, as well as novel functional entities generated by fusion to enzymes, tags (Cloutier et al., 2000) or fluorescent proteins (Casey et al., 2000) . While antibody fragments selected from display libraries have been reformatted as full-length antibodies for catalog sale (Kehoe et al., 2006) , the potential utility of other formats as commercial therapeutics has been limited. One particularly useful format enabled by the work described here is recombinant intrinsically fluorescent antibodies, which have the potential to be widely used in flow cytometry and immunofluorescence. These could replace chemically labeled fluorescent antibodies, which suffer from a number of problems including variability in labeling efficiency, inactivation and quenching (Haugland, 1995; Vira et al., 2010) . In this study, we build on previous efforts (Markiv et al., 2011a,b) aimed at ameliorating these problems by showing that: (i) the VL-FP-VH orientation can also be used (in addition to the original VH-FP-VL orientation); (ii) additional scFvs can be effectively modified in this way; (iii) suitable FPs are not limited to those described by Markiv et al. but also include TGP, an extremely stable monomeric fluorescent protein (Close et al., 2015) ; (iv) scFPs can be effectively displayed on yeast, where they function similarly to their corresponding scFv counterparts, opening the possibility to selecting variants with improved properties either directly from naïve, or preselected, libraries; and (v) functional expression levels of scFPs in the bacterial cytoplasm are relatively high and can rescue some scFvs otherwise expressed at low levels in the periplasm. This was particularly true of the anti-TyrS scFv, which has been challenging to use in the past due to poor expression levels and a propensity to aggregate. The expression level of the scFP version was dramatically higher than the scFv version, increasing by nearly 10-fold (6 vs 0.7 mg/ml). While we have previously demonstrated the value of TGP as a fluorescent protein (Close et al., 2015) , we have not compared the properties of scFPs made using TGP with others such as sfGFP or those used by Markiv et al. (2011a,b) (monomeric red fluorescent protein; blue, cerulean and citrine fluorescent proteins). The ability to crystallize one scTGP construct, as well as express the others within the normal E. coli cytoplasm (i.e. without the need for specialized strains with thioredoxin reductase and glutathione reductase mutations), suggests increased stability of the scTGP construct. However, further experiments to confirm this increased stability will be required. TGP is a monomeric fluorescent protein amenable to crystallization. These features provide unique and valuable characteristics to scTGP molecules for their use in protein chemistry. In addition to utility in downstream assays such as immunofluorescence and flow cytometry, the intrinsic fluorescence of the molecules allows straightforward assessment of expression levels, monitoring of protein purification steps, and antigen recognition. The one step FLISA utilized here saves time and improves the utility of antibodies produced in this format. We also describe the use of the scTGP proteins for epitope binning, a useful and easy technique if the antigen is multimeric that capitalizes on the monomeric and fluorescent properties of the scTGP constructs to assess and develop noncompetitive sets of antigen detection proteins. IgGs in general have higher affinity for the antigen than the corresponding scFvs, since IgGs have two copies of VH-VL and scFPs have one. Therefore, eventual competition between the two antibody formats is strong and easy to detect. Our ongoing work includes development of an LFAbased detection system for plague using antibodies YP2 and YP8, identified as orthogonal binder pairs using the scTGP displacement assay described here . A critical result obtained in this study was the observation that the affinity values for the scFv and scTGP formats of the antibodies were very similar, providing an additional indication that the addition of fluorescent protein added utility without decreasing antibody functionality. However, the display levels of scTGP on the yeast surface were significantly lower compared to the display of the scFv and required additional induction time (∼48 vs 12-16 h for scFvs) to increase the fluorescence of yeast displaying scTGPs by ∼20%, as shown in Supplementary Fig. S1 , available at PEDS online. This extended time likely reflects the need for additional time to fold the larger scFP molecules, or mature the fluorophore, and may vary depending upon the scFv sequence. Therefore, the development of high-throughput methods to select scFvs suitable for conversion to scTGP would be highly advantageous. Interactions between the folding of the FP and the VH, VL domains are difficult to predict. For example, yields may be improved by other robustly folding fluorescent proteins such as superfolder GFP (Pédelacq et al., 2006) , which was specifically selected to avoid interfering with the folding of fused domains. The availability of several, alternative, robustly folded fluorescent proteins to serve as linkers should extend the applicability of the approach described . Attempts to obtain crystal structures of scTGP complexed with 3 versions of the 17mer antigen peptides were unsuccessful. The 17mer peptide sequence was LYEELHVYSPIYSALED and peptides containing the first tyrosine phosphorylated (p1-17), the second tyrosine phosphorylated (p2-17), and both first and second tyrosines phosphorylated p12-17 were selected for crystallization experiments based on ELISA, FLISA and flow cytometry studies with peptides of varying lengths. Over 800 screening conditions were attempted to obtain co-crystals of scTGP and these peptides but resulted in no crystal hits. Soaking apo-scTGP crystals in peptide-containing mother liquors shattered and dissolved crystals almost instantaneously, and crystal pieces harvested after flash-soaking in these solutions did not diffract. These observations suggest that strong interactions exist between scTGP and its antigen peptides. Such interactions are likely to induce substantial conformational changes between the scFv domains causing deformation of the crystal lattice of the apo-scTGP crystal. The bound peptides could also interfere with crystal formation in the case of co-crystallization trials. Systematic peptide construct screening may be required to obtain the co-crystals of the scTGP and its antigen peptides. One of the major problems faced by scFvs identified using display technologies is the quality, quantity and stability of purified scFv protein available for downstream characterization. E. coli periplasmic expression produces limited quantities of scFv, which can lead to poorly purified, aggregated and unstable protein (Arbabi-Ghahroudi et al., 2005; Arndt et al., 1998) , which is why scFvs are not widely used as research reagents. N-and C-terminal FPs require additional flexible linkers that are prone to proteolytic cleavage resulting in potential decoupling of binding from fluorescence. scFv constructs use a flexible linker to connect the VL and VH regions of the scFv, while in naturally occurring IgGs, the VH/VL interaction is stabilized by CH1 and CL. It is possible that the use of a fluorescent protein as connector between the VL and VH domains of a scFv may promote greater stability by mimicking the Fab architecture of natural IgGs, while also providing the added biotechnological functionality of intrinsic fluorescence. The additional stability provided in this orientation relative to N-and C-terminal constructs may promote crystallization through minimization of interdomain flexibility. The crystal structure reported here provides some evidence to support this concept, as the scFv version of the scFP was previously refractory to crystallization, and within the structure, the TGP is found in close proximity to the lower scFv interface. In conclusion, we report that the scTGP format holds promise for the development of robust and readily expressible antibody fragments with a wide variety of uses in research and clinical settings. Supplementary data are available at PEDS online. Monoclonal Antibody Protocols Development of antiyersinia pestis human antibodies with features required for diagnostic and therapeutic applications Quality control of antibodies for assay development Selection and characterization of FceRI phospho-ITAM specific antibodies Selection and verification of antibodies against the cytoplasmic domain of M2 of influenza, a transmembrane protein Authors would like to acknowledge Dr Thomas Terwilliger for his guidance. We would like to thank the staff at the beam line 5. No potential conflicts of interest were disclosed.