» Articles » PMID: 27072057

Accessible Mannitol-Based Amphiphiles (MNAs) for Membrane Protein Solubilisation and Stabilisation

Overview
Journal Chemistry
Specialty Chemistry
Date 2016 Apr 14
PMID 27072057
Citations 30
Authors
Affiliations
Soon will be listed here.
Abstract

Integral membrane proteins are amphipathic molecules crucial for all cellular life. The structural study of these macromolecules starts with protein extraction from the native membranes, followed by purification and crystallisation. Detergents are essential tools for these processes, but detergent-solubilised membrane proteins often denature and aggregate, resulting in loss of both structure and function. In this study, a novel class of agents, designated mannitol-based amphiphiles (MNAs), were prepared and characterised for their ability to solubilise and stabilise membrane proteins. Some of MNAs conferred enhanced stability to four membrane proteins including a G protein-coupled receptor (GPCR), the β2 adrenergic receptor (β2 AR), compared to both n-dodecyl-d-maltoside (DDM) and the other MNAs. These agents were also better than DDM for electron microscopy analysis of the β2 AR. The ease of preparation together with the enhanced membrane protein stabilisation efficacy demonstrates the value of these agents for future membrane protein research.

Citing Articles

Unsymmetric Triazine-Based Triglucoside Detergents for Membrane Protein Stability.

Ehsan M, Ghani L, Lan B, Katsube S, Poulsen I, Zhang X Chembiochem. 2025; 26(5):e202400958.

PMID: 39779472 PMC: 11875885. DOI: 10.1002/cbic.202400958.


Rational Approach to Improve Detergent Efficacy for Membrane Protein Stabilization.

Yoon S, Bae H, Hariharan P, Nygaard A, Lan B, Woubshete M Bioconjug Chem. 2024; 35(2):223-231.

PMID: 38215010 PMC: 10970486. DOI: 10.1021/acs.bioconjchem.3c00507.


Melamine-cored glucosides for membrane protein solubilization and stabilization: importance of water-mediated intermolecular hydrogen bonding in detergent performance.

Ghani L, Kim S, Ehsan M, Lan B, Poulsen I, Dev C Chem Sci. 2023; 14(45):13014-13024.

PMID: 38023530 PMC: 10664503. DOI: 10.1039/d3sc03543c.


Molecular Mechanisms behind Conformational Transitions of the Influenza Virus Hemagglutinin Membrane Anchor.

Michalski M, Setny P J Phys Chem B. 2023; 127(44):9450-9460.

PMID: 37877534 PMC: 10641832. DOI: 10.1021/acs.jpcb.3c05257.


Synthesis, Self-Assembly Properties, and Degradation Characterization of a Nonionic Photocleavable Azo-Sulfide Surfactant Family.

Brown K, Gugger M, Roberts D, Moreno D, Chae P, Ge Y Langmuir. 2023; 39(4):1465-1473.

PMID: 36638323 PMC: 10164600. DOI: 10.1021/acs.langmuir.2c02820.


References
1.
White S, Wimley W . Membrane protein folding and stability: physical principles. Annu Rev Biophys Biomol Struct. 1999; 28:319-65. DOI: 10.1146/annurev.biophys.28.1.319. View

2.
Garavito R, Ferguson-Miller S . Detergents as tools in membrane biochemistry. J Biol Chem. 2001; 276(35):32403-6. DOI: 10.1074/jbc.R100031200. View

3.
Bowie J . Stabilizing membrane proteins. Curr Opin Struct Biol. 2001; 11(4):397-402. DOI: 10.1016/s0959-440x(00)00223-2. View

4.
Mansoor S, Mchaourab H, Farrens D . Mapping proximity within proteins using fluorescence spectroscopy. A study of T4 lysozyme showing that tryptophan residues quench bimane fluorescence. Biochemistry. 2002; 41(8):2475-84. DOI: 10.1021/bi011198i. View

5.
Chen L, Pomroy N, Hwang P, Go S, Chakrabartty A, Prive G . Lipopeptide detergents designed for the structural study of membrane proteins. Nat Biotechnol. 2003; 21(2):171-6. DOI: 10.1038/nbt776. View