Difference between revisions of "2020Ho CryoID"
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Latest revision as of 08:44, 4 June 2020
Citation
Ho, C.-M.; Li, X.; Lai, M.; Terwilliger, T. C.; Beck, J. R.; Wohlschlegel, J.; Goldberg, D. E.; Fitzpatrick, A. W. P. & Zhou, Z. H. Bottom-up structural proteomics: cryoEM of protein complexes enriched from the cellular milieu. Nature methods, 2020, 17, 79-85
Abstract
X-ray crystallography often requires non-native constructs involving mutations or truncations, and is challenged by membrane proteins and large multicomponent complexes. We present here a bottom-up endogenous structural proteomics approach whereby near-atomic-resolution cryo electron microscopy (cryoEM) maps are reconstructed ab initio from unidentified protein complexes enriched directly from the endogenous cellular milieu, followed by identification and atomic modeling of the proteins. The proteins in each complex are identified using cryoID, a program we developed to identify proteins in ab initio cryoEM maps. As a proof of principle, we applied this approach to the malaria-causing parasite Plasmodium falciparum, an organism that has resisted conventional structural-biology approaches, to obtain atomic models of multiple protein complexes implicated in intraerythrocytic survival of the parasite. Our approach is broadly applicable for determining structures of undiscovered protein complexes enriched directly from endogenous sources.
Keywords
Links
https://www.nature.com/articles/s41592-019-0637-y
