4.5 Editorial Material

Structure and function of proteins in membranes and nanodiscs

Journal

BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES
Volume 1863, Issue 1, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.bbamem.2020.183445

Keywords

Membrane proteins; Native nanodiscs; Styrene-maleic acid; SMALP; Transmembrane protein

Funding

  1. Campus Alberta Innovation Program [RCP-12-002C]
  2. Alberta Prion Research Institute/Alberta Innovates Bio Solutions [201600018]
  3. NSERC [2018-04994, 2018-00620]
  4. Natural Sciences and Engineering Research Council of Canada-NSERC [RGPIN-2016-06478]
  5. CIHR/NSERC [SOF-549297-2019]
  6. CIHR [VR3 - 172655]

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The field of membrane structural biology is rapidly evolving, with developments such as native nanodiscs and memteins changing the way we understand biological membranes. Tools like cryo-electron microscopy, X-ray crystallography, and nuclear magnetic resonance spectroscopy are advancing, but challenges remain in understanding how lipids and ligands interact at an atomic level.
The field of membrane structural biology represents a fast-moving field with exciting developments including native nanodiscs that allow preparation of complexes of post-translationally modified proteins bound to biological lipids. This has led to conceptual advances including biological membrane:protein assemblies or memteins as the fundamental functional units of biological membranes. Tools including cryo-electron microscopy and X-ray crystallography are maturing such that it is becoming increasingly feasible to solve structures of large, multicomponent complexes, while complementary methods including nuclear magnetic resonance spectroscopy yield unique insights into interactions and dynamics. Challenges remain, including elucidating exactly how lipids and ligands are recognized at atomic resolution and transduce signals across asymmetric bilayers. In this special volume some of the latest thinking and methods are gathered through the analysis of a range of transmembrane targets. Ongoing work on areas including polymer design, protein labelling and microfluidic technologies will ensure continued progress on improving resolution and throughput, providing deeper understanding of this most important group of targets.

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