TY - JOUR
T1 - Advancing High-Resolution Imaging of Virus Assemblies in Liquid and Ice
AU - Dicecco, Liza Anastasia
AU - Berry, Samantha
AU - Jonaid, G. M.
AU - Solares, Maria J.
AU - Kaylor, Liam
AU - Gray, Jennifer L.
AU - Bator, Carol
AU - Dearnaley, William J.
AU - Spilman, Michael
AU - Dressel-Dukes, Madeline J.
AU - Grandfield, Kathryn
AU - McDonald Esstman, Sarah M.
AU - Kelly, Deborah F.
N1 - Publisher Copyright:
© 2022 JoVE Journal of Visualized Experiments.
PY - 2022/7
Y1 - 2022/7
N2 - Interest in liquid-electron microscopy (liquid-EM) has skyrocketed in recent years as scientists can now observe real-time processes at the nanoscale. It is extremely desirable to pair high-resolution cryo-EM information with dynamic observations as many events occur at rapid timescales-in the millisecond range or faster. Improved knowledge of flexible structures can also assist in the design of novel reagents to combat emerging pathogens, such as SARS-CoV-2. More importantly, viewing biological materials in a fluid environment provides a unique glimpse of their performance in the human body. Presented here are newly developed methods to investigate the nanoscale properties of virus assemblies in liquid and vitreous ice. To accomplish this goal, well-defined samples were used as model systems. Side-by-side comparisons of sample preparation methods and representative structural information are presented. Sub-nanometer features are shown for structures resolved in the range of ~3.5-Å-10 Å. Other recent results that support this complementary framework include dynamic insights of vaccine candidates and antibody-based therapies imaged in liquid. Overall, these correlative applications advance our ability to visualize molecular dynamics, providing a unique context for their use in human health and disease.
AB - Interest in liquid-electron microscopy (liquid-EM) has skyrocketed in recent years as scientists can now observe real-time processes at the nanoscale. It is extremely desirable to pair high-resolution cryo-EM information with dynamic observations as many events occur at rapid timescales-in the millisecond range or faster. Improved knowledge of flexible structures can also assist in the design of novel reagents to combat emerging pathogens, such as SARS-CoV-2. More importantly, viewing biological materials in a fluid environment provides a unique glimpse of their performance in the human body. Presented here are newly developed methods to investigate the nanoscale properties of virus assemblies in liquid and vitreous ice. To accomplish this goal, well-defined samples were used as model systems. Side-by-side comparisons of sample preparation methods and representative structural information are presented. Sub-nanometer features are shown for structures resolved in the range of ~3.5-Å-10 Å. Other recent results that support this complementary framework include dynamic insights of vaccine candidates and antibody-based therapies imaged in liquid. Overall, these correlative applications advance our ability to visualize molecular dynamics, providing a unique context for their use in human health and disease.
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U2 - 10.3791/63856
DO - 10.3791/63856
M3 - Article
C2 - 35938795
AN - SCOPUS:85134715924
SN - 1940-087X
VL - 2022
JO - Journal of Visualized Experiments
JF - Journal of Visualized Experiments
IS - 185
M1 - e63856
ER -