Exploring cryo-electron microscopy with molecular dynamics

Author:

Vant John W.1ORCID,Sarkar Daipayan12ORCID,Nguyen Jonathan1ORCID,Baker Alexander T.13ORCID,Vermaas Josh V.2ORCID,Singharoy Abhishek1ORCID

Affiliation:

1. Biodesign Center for Applied Structural Discovery, Arizona State University, Tempe, AZ 85281, USA

2. MSU-DOE Plant Research Laboratory, Michigan State University, East Lansing, MI 48824, USA

3. Center for Individualized Medicine, Mayo Clinic, Rochester, MN 55905, USA

Abstract

Single particle analysis cryo-electron microscopy (EM) and molecular dynamics (MD) have been complimentary methods since cryo-EM was first applied to the field of structural biology. The relationship started by biasing structural models to fit low-resolution cryo-EM maps of large macromolecular complexes not amenable to crystallization. The connection between cryo-EM and MD evolved as cryo-EM maps improved in resolution, allowing advanced sampling algorithms to simultaneously refine backbone and sidechains. Moving beyond a single static snapshot, modern inferencing approaches integrate cryo-EM and MD to generate structural ensembles from cryo-EM map data or directly from the particle images themselves. We summarize the recent history of MD innovations in the area of cryo-EM modeling. The merits for the myriad of MD based cryo-EM modeling methods are discussed, as well as, the discoveries that were made possible by the integration of molecular modeling with cryo-EM. Lastly, current challenges and potential opportunities are reviewed.

Publisher

Portland Press Ltd.

Subject

Biochemistry

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