key: cord-0984303-54kb2f3o authors: Leslie, Sabrina R. title: Biophysical Reviews ‘Meet the Editors Series’ — a profile of Sabrina Leslie date: 2022-04-13 journal: Biophys Rev DOI: 10.1007/s12551-022-00948-4 sha: 3f3fd3719964a224036fa6edfd20fd1afd90bf4c doc_id: 984303 cord_uid: 54kb2f3o It is my pleasure to introduce myself to the readers of Biophysical Reviews as part of the ‘Meet the Editors Series’. I began my undergraduate studies in the Science One Program at the University of British Columbia (UBC) in 1998, in Vancouver, BC, Canada (Fig. 1 ). This honours programme integrated first-year undergraduate courses in mathematics, physics, chemistry, and biology in a unique way. Four professors and instructors, together with sixty or so keen students, gathered daily in one large room to engage in lectures and tutorials. This inspired a culture of curiosity and questioning assumptions, appreciation of cross-disciplinary approaches and perspectives, and flow of conversations, projects, and friendships. Following this positive experience and my appreciation of the interactions enabled by smaller honours programmes, I pursued my B.Sc. in Honours Physics and Mathematics. Not only did this programme offer challenging courses with stimulating peer groups, but also it provided the quantitative tools and rigorous foundation necessary to explore a wide array of research. I enjoyed thinking and problem solving, was encouraged by my professors to follow my intuition and talent for physics, and this settled my decision to continue in scientific research rather than music as a profession -although I have continued to play the oboe in amateur orchestras over the years. Complementing By the end of my first year, I selected to focus my graduate studies on atomic molecular and optical (AMO) physics with Drs. Dan Stamper-Kurn and Birgitta Whaley who were developing high-resolution imaging and theoretical tools to study the spin dynamics of quantum gases at ultra-high vacuum and zero kelvin. I was attracted by investigating what had never been seen before, the precision and control of these experiments -but was aware that what I was working on was actually colder than deep space. The experience of designing and building instrumentation which ranged from lasers, to magnetic and optical traps, to high-voltage electronics, balanced with theoretical modelling and quantitative understanding of our imaging results, gave me the strong training as an experimental physicist that I sought. Over time, though, cold atomic physics felt increasingly remote and while I enjoyed the challenge, my curiosities shifted closer to life. I'd always been fascinated by biology, particularly at the small scale -molecular and cellular biology. How do lifepreserving processes work? How our cells divide and replicate? How does our DNA get repaired? And how does all this happen in such a robust way? Towards the end of my PhD, I began to explore Biophysics sessions of the American Physics Society (APS) Annual March meeting rather than the AMO sessions, for example. In 2008, I made the decision to accept a Mary Fieser Postdoctoral Fellowship in the Department of Chemistry and Chemical Biology at Harvard University with Adam Cohen and to switch fields. It was there that I got into biophysics, and in everything I did I just kept wanting to take a closer look. That inspiration is the origin of the next steps of my career in biophysics and biotechnology development. My postdoctoral work at Harvard University aimed to address widely recognized shortcomings of existing singlemolecule techniques due to their requirement for complex surface-tethering chemistry or applied electromagnetic fields that introduced variability and altered the behaviour of the molecules. To overcome these limitations, I developed a novel confinement technique that was able to produce the first high-quality images of individual, freely diffusing and interacting molecules in out-of-equilibrium, cell-like conditions (Leslie et al. 2010; Shaheen et al. 2022 (Leslie et al. 2010) . I was very grateful for this appreciation of my work and for my supervisor's encouragement to apply for an Assistant Professor position which popped up at McGill University shortly after this meeting. I am grateful for his advice and support to take my preliminary data and innovations and to build a lab of my own. Without this confidence and push, and the opportunity to attend this GRC meeting in Italy, I may have been hesitant to take that important step and at the right time. At McGill, I had the opportunity to found and lead my first independent research team and lab, replete with many lessons and growth experiences (Fig. 2) . Over the next ten years, we developed CLiC imaging into a platform and used it for new single-molecule studies of nucleic acids and their interactions (Henkin et al. 2016 ) and how these interactions are mediated by DNA structure (Scott et al. 2018 (Scott et al. , 2019 ; . I am especially interested in collaborative projects directed towards the development and optimization of genetic medicines and RNA vaccines, and their delivery systems using these insights. Over the past ten years, I have enjoyed publishing 32 peer-reviewed papers and travelling to give 70 invited presentations in different corners of the world. Since 2009, I have also been the lead inventor on 4 patents (2 awarded, 2 pending), which are now exclusively licensed by Harvard and McGill Universities to our biotech start-up, ScopeSys, who are supportive partners in our vision for the translation of our work to practice. In the midst of the pandemic, I moved my lab to the interdisciplinary Michael Smith Laboratory (MSL) at UBC to take up a joint position bridging this biotechnology hub, the Physics and Astronomy Department, and the School of Biomedical Engineering. I am now working at the leading edge of my field, pioneering high-resolution imaging techniques that are supporting drug and vaccine discovery and development. This work is in close touch with collaborators and partners who are concentrated in Vancouver and California. I am excited to have established active collaborations with academic and private sector partners who helped to pioneer the lipid nanoparticle (LNP) delivery systems that were used in the Pfizer and Moderna mRNA vaccines approved during the COVID-19 pandemic such as Dr. Pieter Cullis (UBC Biochemistry). This collaboration led to our recent publication in ACS Nano of a novel method for simultaneous measurement of LNP size and RNA loading (Kamanzi et al. 2021) . Single-particle imaging of mRNA-LNPs is especially important because the per-particle mRNA-loading can be on the order of unity for standard vaccine formulations, and their structural and dynamic properties are functional but not yet optimized. Through these collaborations and others, my team and I are excited to work at the interface of singlemolecule biophysics and therapeutics. Our vision is to apply our 'bottom-up' microscopy measurements of the biophysics of interactions of biomolecules, in combination with multi-level measurements (in cells and tissues, and the results of clinical trials), to accelerate and advance genetic medicines and vaccines. Outreach is an energizing dimension of my work. I am passionate about science and sharing my curiosity and dedication to discovery. Public advocacy for science and supporting the next generation of scientists is also important to me. I especially enjoy speaking to and interacting with diverse audiences, for example as the keynote speaker at the 2020 I believe in active mentoring and consciously building a positive culture. I value listening, forming teams, and emphasizing communication with an adaptive style. My research requires training in optics, molecular and cell biology, instrumentation, micro/nanodesign and fabrication, and computational, theoretical, and data analysis and I enjoy mentoring all of these (Fig. 3) . Leadership is a growing dimension of my career. In particular, I appreciate the chance to listen and support young women entering as well as considering STEM careers. For example, when I joined the McGill Physics Department, I identified a need for a Women in Physics Committee, to engage with and support diversity in science, founded this committee, and energized its growth. At a more junior level, I visited my former high school to accept their Junior Alumni Achievement Award, which was an honour but what I valued even more was the opportunity to meet with women students there to offer my encouragement for pursuing careers in science, technology, and entrepreneurship. Curriculum is another vehicle through which I lead change. I lead the design of the Biophysics Streams-Majors and Honours for McGill Physics, which is now established and guiding students. Recently I hosted Biophysics Day for the four biophysics groups within UBC Physics and Astronomy to share our science and meet one another in person. I am excited to be working at the interface between biophysics and therapeutics communities, at a time when our single-molecule and single-cell imaging tools may help us guard against future pandemics, and to be doing this work in my home in BC. In closing, I am grateful to the readers of Biophysical Review to share this story of my career. I look forward to, in my role as an Editorial Board Member, inviting, reviewing, and handling articles on your research. Continuous confinement fluidics: getting lots of molecules into small spaces with high fidelity Open-frame system for single-molecule microscopy Miniaturized flow cell with pneumaticallyactuated vertical nanoconfinement for single-molecule imaging and manipulation Precision platform for convex lens-induced confinement microscopy (2013) Precision platform for convex lens-induced confinement microscopy Convex lensinduced nanoscale templating Single-molecule fluorescence imaging of processive myosin with enhanced background suppression using linear zero-mode waveguides (ZMWs) and convex lens induced confinement (CLIC) Manipulating and visualizing molecular interactions in customized nanoscale spaces Parallelized cytoindentation using convex micropatterned surfaces Simultaneous, single-particle measurements of size and loading give insights into the structure of drug-delivery nanoparticles Free energy of a polymer in slit-like confinement from the Odijk regime to the bulk Convex lens-induced confinement for imaging single molecules Development of a platform for single cell genomics using convex lens-induced confinement Visualizing structure-mediated interactions in supercoiled DNA molecules Single-molecule visualization of the effects of ionic strength and crowding on structure-mediated interactions in supercoiled DNA molecules Non-equilibrium structural dynamics of supercoiled DNA plasmids exhibits asymmetrical relaxation Probing inhomogeneous diffusion in the microenvironments of phase-separated polymers under confinement Single-cell analysis for drug development using convex lens-induced confinement imaging The author declares no competing interests.