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Studying membrane proteins with MicroED

Journal

BIOCHEMICAL SOCIETY TRANSACTIONS
Volume 50, Issue 1, Pages 231-239

Publisher

PORTLAND PRESS LTD
DOI: 10.1042/BST20210911

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Funding

  1. National Institutes of Health [P41GM136508]
  2. Howard Hughes Medical Institute

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The structural investigation of biological macromolecules is crucial for understanding disease mechanisms. MicroED is an effective technique for solving difficult sample structures, but membrane proteins remain a challenge.
The structural investigation of biological macromolecules is indispensable in understanding the molecular mechanisms underlying diseases. Several structural biology techniques have been introduced to unravel the structural facets of biomolecules. Among these, the has produced atomic resolution structures of important biological and small molecules. Since its inception in 2013, MicroED established a demonstrated ability for solving structures of difficult samples using vanishingly small crystals. However, membrane proteins remain the next big frontier for MicroED. The intrinsic properties of membrane proteins necessitate improved sample handling and imaging techniques to be developed and optimized for MicroED. Here, we summarize the milestones of electron crystallography of two-dimensional crystals leading to MicroED of three-dimensional crystals. Then, we focus on four different membrane protein families and discuss representatives from each family solved by MicroED.

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