TY - JOUR
T1 - Automated Tools to Advance High-Resolution Imaging in Liquid
AU - Jonaid, G. M.
AU - Casasanta, Michael A.
AU - Dearnaley, William J.
AU - Berry, Samantha
AU - Kaylor, Liam
AU - Dressel-Dukes, Madeline J.
AU - Spilman, Michael S.
AU - Gray, Jennifer L.
AU - Kelly, Deborah F.
N1 - Publisher Copyright:
Copyright © The Author(s), 2022. Published by Cambridge University Press on behalf of the Microscopy Society of America.
PY - 2022/4/11
Y1 - 2022/4/11
N2 - Liquid-electron microscopy (EM), the room-temperature correlate to cryo-EM, is a rapidly growing field providing high-resolution insights of macromolecules in solution. Here, we describe how liquid-EM experiments can incorporate automated tools to propel the field to new heights. We demonstrate fresh workflows for specimen preparation, data collection, and computing processes to assess biological structures in liquid. Adeno-associated virus (AAV) and the SARS-CoV-2 nucleocapsid (N) were used as model systems to highlight the technical advances. These complexes were selected based on their major differences in size and natural symmetry. AAV is a highly symmetric, icosahedral assembly with a particle diameter of ~25 nm. At the other end of the spectrum, N protein is an asymmetric monomer or dimer with dimensions of approximately 5-7 nm, depending upon its oligomerization state. Equally important, both AAV and N protein are popular subjects in biomedical research due to their high value in vaccine development and therapeutic efforts against COVID-19. Overall, we demonstrate how automated practices in liquid-EM can be used to decode molecules of interest for human health and disease.
AB - Liquid-electron microscopy (EM), the room-temperature correlate to cryo-EM, is a rapidly growing field providing high-resolution insights of macromolecules in solution. Here, we describe how liquid-EM experiments can incorporate automated tools to propel the field to new heights. We demonstrate fresh workflows for specimen preparation, data collection, and computing processes to assess biological structures in liquid. Adeno-associated virus (AAV) and the SARS-CoV-2 nucleocapsid (N) were used as model systems to highlight the technical advances. These complexes were selected based on their major differences in size and natural symmetry. AAV is a highly symmetric, icosahedral assembly with a particle diameter of ~25 nm. At the other end of the spectrum, N protein is an asymmetric monomer or dimer with dimensions of approximately 5-7 nm, depending upon its oligomerization state. Equally important, both AAV and N protein are popular subjects in biomedical research due to their high value in vaccine development and therapeutic efforts against COVID-19. Overall, we demonstrate how automated practices in liquid-EM can be used to decode molecules of interest for human health and disease.
UR - http://www.scopus.com/inward/record.url?scp=85123981161&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85123981161&partnerID=8YFLogxK
U2 - 10.1017/S1431927621013921
DO - 10.1017/S1431927621013921
M3 - Article
C2 - 35048845
AN - SCOPUS:85123981161
SN - 1431-9276
VL - 28
SP - 361
EP - 370
JO - Microscopy and Microanalysis
JF - Microscopy and Microanalysis
IS - 2
ER -