key: cord-0833384-u8993exd
authors: Cotabarren, Juliana; Claver, Santiago; Payrol, Juan Abreu; Garcia-Pardo, Javier; Obregón, Walter David
title: Purification and Characterization of a Novel Thermostable Papain Inhibitor from Moringa oleifera with Antimicrobial and Anticoagulant Properties
date: 2021-04-08
journal: Pharmaceutics
DOI: 10.3390/pharmaceutics13040512
sha: a3d0901ecc4113e3311a0bc93ed6b9a4cdaa5e35
doc_id: 833384
cord_uid: u8993exd

Plant cystatins (or phytocystatins) comprise a large superfamily of natural bioactive small proteins that typically act as protein inhibitors of papain-like cysteine proteases. In this report, we present the purification and characterization of the first phytocystatin isolated from Moringa oleifera (MoPI). MoPI has a molecular mass of 19 kDa and showed an extraordinary physicochemical stability against acidic pHs and high temperatures. Our findings also revealed that MoPI is one of the most potent cysteine protease inhibitors reported to date, with Ki and IC(50) values of 2.1 nM and 5.7 nM, respectively. More interestingly, MoPI presents a strong antimicrobial activity against human pathogens such as Enterococcus faecalis and Staphylococcus aureus. In addition, MoPI also showed important anticoagulant activity, which is an unprecedented property for this family of protease inhibitors. These results highlight the pharmaceutical potential of this plant and its derived bioactive molecules.

Moringa oleifera (M. oleifera) is a plant native to India that grows in the tropical and subtropical regions of the world. Due to its high nutritional properties, the whole plant is typically used for nutritional or commercial purposes. It is worth mentioning that different parts of this tree are applied as food to combat malnutrition, especially among infants and breastfeeding woman in many developing countries, including India, Pakistan, the Philippines, Hawaii and many regions of Africa [1] .

In addition to its nutritional value, M. oleifera has an important medicinal and pharmacological potential. Recent studies have shown that extracts of this plant possess strong antioxidant, anticancer, anti-inflammatory and antidiabetic properties [2] . Furthermore, evidence suggests that almost all parts of the plant exhibit antibacterial activity [3] . In many cases, such antibacterial activity has been associated with the presence of small chemical compounds such as glucosinolates (β-thioglucoside N-hydroxysulfates), isothiocyanates, organic carbamates, chalcone-oxazolidinone hybrids and thiocarbamate [4] . Although extensive research has been carried out with M. oleifera extracts, little is known regarding the presence of protease inhibitors in this plant and their role as antibacterial agents. 0.01 M phosphate buffer, pH 7.4 in an ice bath to avoid possible protein denaturation. After incubation for 2 h at room temperature, the mixture was filtered with gauze, and the insoluble material was removed by centrifugation for 30 min at 7000× g at 4 • C. The clarified supernatant (from now on: MoCE) was collected and immediately frozen at −20 • C until analysis. The total protein content was determined by the Bradford's assay [24] , as described by Cotabarren et al. [25] using bovine serum albumin (BSA) as standard (0.1 mg/mL). Papain inhibitory activity was determined as described in Section 2.4.

According to our previous studies, protease inhibitors present high physicochemical stability with minimal loss of inhibitory activity [26] . Accordingly, in the first purification step, the crude extract was subjected to 100 • C for 15, 60, and 120 min. Afterward, the samples were cooled at room temperature, and the thermally denatured proteins were removed by centrifugation for 30 min at 7000× g and 4 • C. The total protein content and the inhibitory activity of the non-treated crude extract and heat-treated samples were determined. Each obtained sample was called MoHT15, MoHT60 and MoHT120, in accordance to the incubation time.

A sample of 150 mL of MoHT15 was loaded onto a papain-glyoxyl-agarose column prepared in-house following the method of Obregón and colleagues [27] (1.5 × 12 cm) connected to an Äkta-Purifier (GE Healthcare, Chicago, IL, USA) previously equilibrated with 0.01M phosphate buffer, pH 5.5-considering the optimal pH for the papain-inhibitor interaction-. After complete removal of the non-retained proteins with equilibration buffer, affiliated proteins were eluted generating a sudden pH change by the addition of 0.01 M HCl, pH 2.5 at a flow rate of 0.7 mL/min. The eluted fractions were immediately neutralized by adding 0.1 M NaOH. The purified papain inhibitor was named MoPI (M. oleifera papain inhibitor). Papain inhibitory activity and protein quantification were determined as previously described. Samples were analysed by SDS-PAGE as described by Cotabarren et al. [25] 2.4. Enzymatic Analysis of the Inhibitory Activity against Papain Papain inhibitory activity was determined by using the substrate L-pyroglutamyl-Lphenylalanyl-L-leucine-p-nitroanilide (PFLNA). The hydrolysis of PFLNA was monitored by measuring the increase of the absorbance at 410 nm at 37 • C every minute for 10 min [27] . Reaction volumes were adapted to a 96-well plate with a final volume of 200 µL. The inhibition of papain activity caused a decrease in the hydrolysis rate of the substrate, which resulted in the attenuation of the hydrolysis slope. The inhibitory activity was estimated as the residual proteolytic activity in the presence of the inhibitor and expressed as a percentage of inhibition in comparison with the control assay (in the absence of the inhibitor). In the case of heat-treated samples, the volume used in each assay was 20 µL.

One papain inhibitory unit (1 PIU) was defined as the decrease in 0.01 unit of absorbance at 410 nm per 10 min assay, at 37 • C. The inhibitory constant (Ki) and the IC 50 (defined as the inhibitor concentration required for half-activity of the enzyme) were calculated according to the protocol described by Tellechea and colleagues [28] , modified for papain inhibition. All measurements were performed in triplicate. equal parts, of 5 healthy individuals, maintained at 37 • C with 3.8% sodium citrate (ratio sample: anticoagulant 9:1) was used as a sample (from now on: PBP).

For the PT test, the commercial Soluplastin reactive (Wiener Lab.) was employed. Initially, equal parts of the PBP sample and the papain inhibitor (12.5 µg/mL) were incubated for 2 min at 37 • C, then 50 µL of Soluplastin were added to 25 µL of this mixture and checked for the coagulation time. For the aPTT test, 25 µL of aPTT (Wiener Lab.) were added to an equal volume of PBP-inhibitor mixture (previously incubated for 2 min at 37 • C). After 2 min incubation at 37 • C, 25 µL of 50 mM CaCl 2 was added to initiate the coagulation time determination. For both assays, measurements were carried out in triplicate and appropriate controls were achieved.

In order to determine the inhibitory capacity on the growth of various bacterial strains by the inhibitor, the agar diffusion assay based on the Kirby-Bauer test was performed with slight modifications [29] . Initially, the pre-inoculums of different pathogenic microorganisms (i.e., Citrobacter amalonaticus, Enterobacter cloacae, Enterococcus faecalis, Escherichia coli, Klebsiella pneumoniae, Proteus vulgaris, Pseudomonas aeruginosa, Salmonella typhimurium and Staphylococcus aureus) were grown at 37 • C for 18-24 h and the turbidity of the bacterial suspension was adjusted with a physiological solution to 0.5 McFarland scale (1.5 × 108 UFC/mL). The inoculums were plated on Müller Hinton agar plates, in which a drop of 10 µL inhibitor was placed. After the drop placed in the plate was dry, the plates were incubated at 37 • C for 24 h. Then, the diameters of the bacterial growth inhibition halos (in millimetres) were measured. The tests were conducted by triplicate, including the respective controls.

Statistical analyses (ANOVA) were performed with GraphPad Prism (v6.03, GraphPad Sofware Inc.: San Diego, CA, USA, 2012). Significant differences between the means of the parameters were determined by Tukey's post-hoc test (p < 0.05).

Moringa seeds are known to be rich sources of lipids (31%), and their elimination leads to a high protein expeller (19%), generating an interesting product for human nutrition. As described in Section 2.2, we prepared a crude extract of M. oleifera seeds (MoCE). The protein concentration of the sample was 3.51 ± 0.03 mg/mL (see Table 1 ), which is in agreement with previous reports [30] . Next, we aimed to investigate the papain inhibitory activity of the crude extract. This initial examination showed that small amounts of MoCE to the reaction tube produce a drastic decrease in the papain activity, which is consistent with the presence of inhibitory molecules in the sample. A more detailed dose-response analysis showed that MoCE strongly inhibits papain with an IC 50 value of 0.025 µg/mL. A number of plant protease inhibitors (PIs) have been purified and found to be stable and active at high temperatures [26, 31] . For this reason, we incubated the MoCE at 100 • C for 15, 60 and 120 min as an initial purification step. As observed in Table 1 , the heat treatment at 100 • C produced a decrease in protein content of 50-60% with respect to the Pharmaceutics 2021, 13, 512 5 of 11 raw starting crude extract. Papain inhibitory activity was then determined in the samples corresponding to each heat treatment (MoHT15, MoHT60 and MoHT120). As shown in Figure 1A , the inhibitory activity against papain was maintained even after 120 min of incubation, suggesting an extraordinary thermostability of the inhibitor. It is worth mentioning that this property is very interesting for most biotechnological applications, behind an added value for their commercial exploitation [32] . ment at 100 °C produced a decrease in protein content of 50-60% with respect to the raw starting crude extract. Papain inhibitory activity was then determined in the samples corresponding to each heat treatment (MoHT15, MoHT60 and MoHT120). As shown in Figure 1A , the inhibitory activity against papain was maintained even after 120 min of incubation, suggesting an extraordinary thermostability of the inhibitor. It is worth mentioning that this property is very interesting for most biotechnological applications, behind an added value for their commercial exploitation [32] .

In addition to the thermal stability, we also evaluated the effect of the temperature on the stability of the inhibitor at two extreme pH values (pH 2 and 9). Surprisingly, after 60 min of incubation, we were able to recover 100% of the inhibitory activity against papain. This unusual physicochemical stability is a remarkable feature for phytocystatins. So far, there is only one previous report describing a papain inhibitor isolated from Vigna unguiculata seeds that presented both thermal stability and a similar tolerance to a wide range of pHs [33] . As shown in Table 1 and Figure 1A , MoHT15 is the sample with a better relationship between conservation of activity/elimination of soluble non-inhibitory proteins. Moreover, this thermal treatment represents a simple and crucial purification step to achieve a partial purification of the inhibitor. MoPI was purified from the MoHT15 fraction after performing a high-speed centrifugation step (see Materials and Methods section for ex- In addition to the thermal stability, we also evaluated the effect of the temperature on the stability of the inhibitor at two extreme pH values (pH 2 and 9). Surprisingly, after 60 min of incubation, we were able to recover 100% of the inhibitory activity against papain. This unusual physicochemical stability is a remarkable feature for phytocystatins. So far, there is only one previous report describing a papain inhibitor isolated from Vigna unguiculata seeds that presented both thermal stability and a similar tolerance to a wide range of pHs [33] .

As shown in Table 1 and Figure 1A , MoHT15 is the sample with a better relationship between conservation of activity/elimination of soluble non-inhibitory proteins. Moreover, this thermal treatment represents a simple and crucial purification step to achieve a partial purification of the inhibitor. MoPI was purified from the MoHT15 fraction after performing a high-speed centrifugation step (see Materials and Methods section for experimental details). After centrifugation, the supernatant containing the inhibitor was further purified by affinity chromatography using a special support based on glyoxyl-agarose containing covalently immobilized papain. After purification by affinity chromatography, the papain inhibitory activity of the eluted fractions was determined. As shown in Figure 1B , the purified inhibitor eluted as a single peak that contained a protein concentration of 0.16 ± 0.01 mg/mL and specific inhibitory activity of 10.81 PIU/mg (see Table 2 ). After the different purification steps, the resultant MoPI showed an apparent molecular weight of 19 kDa ( Figure 1C ). This size is in agreement with the size of other phytocystatins previously isolated from plants (i.e., garlic phytocystatin [34] , Barley protease inhibitor and Vigna unguiculata cysteine inhibitor [33] . a One papain inhibitory unit (1 PIU) was defined as the amount of inhibitor that decreased absorbance at 410 nm by 0.1 under the assay conditions. b The purification index (Purity) was calculated as the ratio between the specific inhibitory activity determined after each purification step as compared to the initial inhibitory activity present in the crude extract. c Yield of inhibitory activity after each purification step compared to the crude extract (%).

Kinetic studies of MoPI inhibition activity were carried out following the protocol described by Tellechea and colleagues [28] . Analysis of the data revealed that MoPI has an IC 50 value of 0.11 µg/mL (5.7 × 10 −9 M, Figure 2A ) and a Ki value of 2.1 × 10 −9 M ( Figure 2B ), indicating that MoPI is a potent papain inhibitor. In comparison to other high thermostable protease inhibitors previously reported in the literature [26] , MoPI presents one of the lowest IC 50 values (see Table 3 ). MoPI also presents a Ki that is significantly lower in comparison to other thermostable PIs; i.e., papaya proteinase inhibitor (Ki = 3 × 10 −7 M; [35] ), Cajanus cajan proteinase inhibitor (2.72 × 10 −7 M, [36] ), Albizia amara protease inhibitor (1.24 × 10 −8 M, [37] ) and garlic protease inhibitor (8.5 × 10 −8 M, [34] ). tor and Vigna unguiculata cysteine inhibitor [33] . a One papain inhibitory unit (1 PIU) was defined as the amount of inhibitor that decreased absorbance at 410 nm by 0.1 under the assay conditions. b The purification index (Purity) was calculated as the ratio between the specific inhibitory activity determined after each purification step as compared to the initial inhibitory activity present in the crude extract. c Yield of inhibitory activity after each purification step compared to the crude extract (%).

Kinetic studies of MoPI inhibition activity were carried out following the protoc described by Tellechea and colleagues [28] . Analysis of the data revealed that MoPI has IC50 value of 0.11 µg/mL (5.7 × 10 −9 M, Figure 2A ) and a Ki value of 2.1 × 10 −9 M (Figure 2 indicating that MoPI is a potent papain inhibitor. In comparison to other high thermos ble protease inhibitors previously reported in the literature [26] , MoPI presents one of t lowest IC50 values (see Table 3 ). MoPI also presents a Ki that is significantly lower in co parison to other thermostable PIs; i.e., papaya proteinase inhibitor (Ki = 3 × 10 −7 M; [35 Cajanus cajan proteinase inhibitor (2.72 × 10 −7 M, [36] ), Albizia amara protease inhibitor (1 × 10 −8 M, [37] ) and garlic protease inhibitor (8.5 × 10 −8 M, [34] ). Interestingly, while most of the phytocystatins maintains only 10-25% of their inh itory capacity after 80-90 °C incubation, MoPI preserves total inhibitory capacity after min incubation at 100 °C, being one of the most stable phytocystatins reported to date (s Table 3 ). Only VuCys1 has a higher thermostability after 60 min incubation at 100 ° However, the inhibitory kinetics of this inhibitor is still unknown. It is important to me tion that although the phytocystatins included in Table 3 were classified by their autho Interestingly, while most of the phytocystatins maintains only 10-25% of their inhibitory capacity after 80-90 • C incubation, MoPI preserves total inhibitory capacity after 15 min incubation at 100 • C, being one of the most stable phytocystatins reported to date (see Table 3 ). Only VuCys1 has a higher thermostability after 60 min incubation at 100 • C. However, the inhibitory kinetics of this inhibitor is still unknown. It is important to mention that although the phytocystatins included in Table 3 were classified by their authors as highly thermostable PIs, we reported on a recently published article [26] that such phytocystatins do not fall within the super stable inhibitors. For this reason, the current stability data, the IC 50 and Ki position MoPI as one of the phytocystatins with the greatest potential for biotechnological applications. Several studies aimed at characterizing the dependence of the thermal stability of plant PIs on pH established the optimal conditions for the application of these proteins to biotechnology involved in the development of transgenic crops resistant to insect pests [38] or in the pharmaceutical industry as specific inhibitors of pathogens such as fungi and bacteria [39] . 

Thrombotic events due to blood clotting are known to pose a serious problem in cardiovascular disease [45] . Although heparin (a protease inhibitor widely used to delay blood clotting time) has been widely used for this purpose, its continued use often results in the development of thrombocytopenia and immune response [46] . Furthermore, other anticoagulant drugs, such as aspirin and clopidogrel, may lead to serious side effects [47] . In this context, only serine protease inhibitors have been studied as potential antithrombotic agents [48] [49] [50] . Discovery of new PIs with inhibitory activity of the coagulation cascade would result in an alternative strategy against thrombosis.

The anticoagulant activity of MoPI was tested by determining the activated partial thromboplastin time and the time of prothrombin ( Table 4 ). The concentration of inhibitor evaluated (12.5 µg/mL) produced a significant increase of 25% in the time of activated partial thromboplastin compared to the control sample. This result suggests a potential application of the M. oleifera papain inhibitor as an anticoagulant agent of natural origin as an alternative to conventional anticoagulant agents. Regarding the behaviour of MoPI for the extrinsic route (see Prothrombin time in Table 4 ), the values obtained for the corresponding test were very similar to those of the control sample; therefore, no significant increase in coagulation time was observed. 

The antimicrobial activity of the crude extract (MoCE) and heat-treated sample (MoHT15) were evaluated in order to establish whether the powerful papain inhibitor from M. oleifera is able to inhibit bacterial growth. As observed in Table 5 , our results confirmed the findings from Bancessi and colleagues [3] that reported a strong antimicrobial activity of Moringa seed extracts against E. coli, E. faecalis, S. aureaus, E. cloacae, Proteus, K. pneumoniae. More interestingly, the heat-treated sample showed a strong inhibitory effect against the growth of E. faecalis and S. aureaus. A similar profile of inhibition was observed for the purified inhibitor MoPI, suggesting that this papain inhibitor has strong Pharmaceutics 2021, 13, 512 8 of 11 antibacterial properties against these two bacterial strains. It should be noted that the tests were performed using a relatively low sample concentration. (++) inhibition zone of 6 mm; (+) inhibition zone of 5 mm; -(no inhibition).

As discussed above, the only known phytocystatin with antibacterial activity is a kiwi cystatin that inhibits the growth of Agrobacterium tumefaciens, Burkholderia cepacia, and Erwinia carotovora [23] . This study represents new evidence of the antimicrobial role of phytocystatins, expanding their possible biomedical applications. Genetically engineered cystatins could be generated and act as potent nutraceuticals in the development of a food product designed from a "plant derivative" that allows preventing the infection of pathogens in the human digestive system. So far there is no evidence that cysteine proteases (absent in the human intestinal system) have any role (as compared to serine proteases) in the degradation of human food. Therefore, plant cystatins would have appropriate characteristics to be used as pharmaceutical products and/or to be incorporated as nutraceuticals due to their antimicrobial and antiviral properties, since they can only interact with microbial or viral cysteine proteases in the human intestine and not with cysteine proteases in the human digestive system [51] .

It is known that, with the aim of getting the properties of Moringa to the consumer, studies are being carried out with different foods, mainly meat products and breads, in which Moringa (leaf, seed, extracts, etc.) is incorporated as an ingredient. In meat products, it is used as a preservative and antioxidant additive with very good results without affecting the sensory characteristics of the final product. In the bakery sector, the objective is usually the nutritional enrichment of the food. It would be very interesting to incorporate Moringa seed extracts as a food additive, substituting different preservatives and chemical antioxidants, and at the same time its use in the preparation of highly nutritious basic products, ideal for certain population groups in greater risk of malnutrition. There are indications that the industry is gearing up for a large investment in "designer foods" with benefits for humans. Such foods, which could ultimately decrease demand for drugs, could also help control disease and disorders often associated with a change in lifestyle.

Herein, we report the isolation and purification of the first papain inhibitor from M. oleifera seeds. This novel bioactive molecule demonstrated a great physicochemical stability at high temperatures and extreme pHs. In addition, MoPI showed a surprising inhibitory activity against papain with Ki and IC 50 values in the nanomolar range, making this inhibitor one of the most powerful phytocystatins found to date. On the other hand, the growth inhibitory capacity was determined on various strains of pathogenic bacteria, demonstrating a strong antimicrobial effect of this inhibitor against Enterococcus faecalis and Staphylococcus aureus strains. Moreover, we also anticipate that MoPI isolated from M. oleifera has intrinsic anticoagulant activity against the intrinsic pathway of the coagula-Pharmaceutics 2021, 13, 512 9 of 11 tion cascade. Taken together, these properties position this novel molecule as a potential natural antibacterial agent suitable for biotechnological and pharmaceutical applications. This research also contributes to the knowledge of unprecedented characteristics in this type of inhibitor, being the first cysteine protease inhibitor of vegetable origin with this particular combination of biological activities. 

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Institutional Review Board Statement: Not applicable.

Data Availability Statement: Not applicable.

The authors declare no conflict of interest.