Literature DB >> 35133709

How physical forces drive the process of helical membrane protein folding.

Karolina Corin1, James U Bowie1.   

Abstract

Protein folding is a fundamental process of life with important implications throughout biology. Indeed, tens of thousands of mutations have been associated with diseases, and most of these mutations are believed to affect protein folding rather than function. Correct folding is also a key element of design. These factors have motivated decades of research on protein folding. Unfortunately, knowledge of membrane protein folding lags that of soluble proteins. This gap is partly caused by the greater technical challenges associated with membrane protein studies, but also because of additional complexities. While soluble proteins fold in a homogenous water environment, membrane proteins fold in a setting that ranges from bulk water to highly charged to apolar. Thus, the forces that drive folding vary in different regions of the protein, and this complexity needs to be incorporated into our understanding of the folding process. Here, we review our understanding of membrane protein folding biophysics. Despite the greater challenge, better model systems and new experimental techniques are starting to unravel the forces and pathways in membrane protein folding.
© 2022 The Authors.

Entities:  

Keywords:  co-translational folding; energetics; folding pathways; helix insertion; membrane protein topology

Mesh:

Substances:

Year:  2022        PMID: 35133709      PMCID: PMC8892262          DOI: 10.15252/embr.202153025

Source DB:  PubMed          Journal:  EMBO Rep        ISSN: 1469-221X            Impact factor:   8.807


  226 in total

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Journal:  Proteins       Date:  2001-12-01

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Journal:  J Biol Chem       Date:  2007-05-08       Impact factor: 5.157

4.  A frequent, GxxxG-mediated, transmembrane association motif is optimized for the formation of interhelical Cα-H hydrogen bonds.

Authors:  Benjamin K Mueller; Sabareesh Subramaniam; Alessandro Senes
Journal:  Proc Natl Acad Sci U S A       Date:  2014-02-25       Impact factor: 11.205

5.  Hydrogen bonding and equilibrium protium-deuterium fractionation factors in the immunoglobulin G binding domain of protein G.

Authors:  D Khare; P Alexander; J Orban
Journal:  Biochemistry       Date:  1999-03-30       Impact factor: 3.162

6.  Lipids and topological rules of membrane protein assembly: balance between long and short range lipid-protein interactions.

Authors:  Heidi Vitrac; Mikhail Bogdanov; Phil Heacock; William Dowhan
Journal:  J Biol Chem       Date:  2011-03-15       Impact factor: 5.157

7.  Phosphatidylglycerol lipids enhance folding of an alpha helical membrane protein.

Authors:  Annela M Seddon; Mark Lorch; Oscar Ces; Richard H Templer; Fiona Macrae; Paula J Booth
Journal:  J Mol Biol       Date:  2008-05-07       Impact factor: 5.469

8.  Knowledge-based potential for positioning membrane-associated structures and assessing residue-specific energetic contributions.

Authors:  Chaim A Schramm; Brett T Hannigan; Jason E Donald; Chen Keasar; Jeffrey G Saven; William F Degrado; Ilan Samish
Journal:  Structure       Date:  2012-05-09       Impact factor: 5.006

9.  Orientational preferences of neighboring helices can drive ER insertion of a marginally hydrophobic transmembrane helix.

Authors:  Karin Ojemalm; Katrin K Halling; Ingmarie Nilsson; Gunnar von Heijne
Journal:  Mol Cell       Date:  2012-01-25       Impact factor: 17.970

10.  Insertion and folding pathways of single membrane proteins guided by translocases and insertases.

Authors:  Tetiana Serdiuk; Anja Steudle; Stefania A Mari; Selen Manioglu; H Ronald Kaback; Andreas Kuhn; Daniel J Müller
Journal:  Sci Adv       Date:  2019-01-30       Impact factor: 14.136

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  1 in total

Review 1.  How physical forces drive the process of helical membrane protein folding.

Authors:  Karolina Corin; James U Bowie
Journal:  EMBO Rep       Date:  2022-02-08       Impact factor: 8.807

  1 in total

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