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Learn how Cryo-Electron Microscopy (Cryo-EM) is used to study the structure of filaments, such as microfilaments, microtubules, and myofilaments, at Creative Biostructure. This process includes sample preparation, negative staining EM, image processing, and 3D reconstruction at near-atomic resolution. The service provides biologically insightful information for understanding biological progress.
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Cryo-Electron Microscopy (Cryo-EM) techniques have been essential
for understanding the structure of biological specimens such as cells,
tissues and macromolecular complexes. Characterizing the molecular
structure of macromolecules is crucial for getting an insight into
understanding of the biochemical and cellular processes. Due to there
is not required crystallization and only small amounts of sample are
needed, Cryo-EM has become a major technique in structural biology
for the studies of functional complexes. Meanwhile, with the
advanced of image processing and three-dimensional reconstruction
techniques, Cryo-EM can also provide a three-dimensional (3D) maps
of biological macromolecules at a near-atomic resolutions.
At Creative Biostructure, our service includes the preparation and
purification of filaments, negative staining EM and image processing of
Cryo-EM, provide the customer with the 3D reconstruction at a near
atomic resolution, and finally provides a biologically insightful for
understanding the biological progress.
References
Eva Nogales, Sjors H.W. Scheres, Cryo-EM: A Unique Tool for the
Visualization of Macromolecular Complexity. Mol Cell, 2015; 58:677-
Lingyun Zhao, Jingfei Xu, et al. Determining the RAD51-DNA
Nucleoprotein Filament Structure and Function by Cryo-Electron
Microscopy. Methods Enzymol, 2018; 600:179-199.
Ahmet Mentesa, Andrew Huehn, et al. High-resolution cryo-EM
structures of actin-bound myosin states reveal the mechanism of
myosin force sensing. Proc Natl Acad Sci U S A. 2018; 115:1292-1297.