Mass spectrometry-A versatile tool for characterising the lipid environment of membrane protein assemblies

被引:23
作者
Frick, Melissa [1 ]
Schmidt, Carla [1 ]
机构
[1] Martin Luther Univ Halle Wittenberg, Inst Biochem & Biotechnol, Charles Tanford Prot Ctr, Interdisciplinary Res Ctr HALOmem, Halle, Germany
关键词
Biological membranes; Lipids; Membrane proteins; Membrane mimetics; Mass spectrometry; Protein-lipid interactions; CYTOCHROME-C-OXIDASE; ELECTROSPRAY-IONIZATION; HYDROGEN/DEUTERIUM EXCHANGE; TRANSMEMBRANE PEPTIDES; SHOTGUN LIPIDOMICS; ANNULAR LIPIDS; DOUBLE-BONDS; SAPOSIN; LIPOSOMES; INTACT;
D O I
10.1016/j.chemphyslip.2019.04.001
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Biological membranes are selectively permeable barriers important for cell organization and compartmentalization. Their organisation strongly depends on the lipids that constitute the lipid bilayer as well as the proteins that reside in the membrane. Unravelling the organisation of biological membranes is therefore of great importance to understand cellular function driven by integral and peripheral membrane proteins. Recent developments in mass spectrometry made it a powerful tool contributing to our present-day understanding of membrane composition and organisation. The two main deliverables of mass spectrometry are (i) the identification and quantification of the membrane components, and (ii) the analysis of their structural arrangements. In this review article, we first briefly discuss the aspects of membrane organization that are accessible through mass spectrometry. We then provide detailed insights into the various mass spectrometric strategies which help identifying lipids from membranes or membrane protein assemblies, unravelling the lipid binding modes in membrane proteins and uncovering their structural roles. We further discuss the growing interest in membrane mimetics providing membrane proteins with a native-like lipid environment for structural and functional studies and the possibilities of mass spectrometry to contribute in these experiments.
引用
收藏
页码:145 / 157
页数:13
相关论文
共 108 条
[1]   Micelles protect membrane complexes from solution to vacuum [J].
Barrera, Nelson P. ;
Di Bartolo, Natalie ;
Booth, Paula J. ;
Robinson, Carol V. .
SCIENCE, 2008, 321 (5886) :243-246
[2]   The role of lipids in defining membrane protein interactions: insights from mass spectrometry [J].
Barrera, Nelson P. ;
Zhou, Min ;
Robinson, Carol V. .
TRENDS IN CELL BIOLOGY, 2013, 23 (01) :1-8
[3]   Advances in the Mass Spectrometry of Membrane Proteins: From Individual Proteins to Intact Complexes [J].
Barrera, Nelson P. ;
Robinson, Carol V. .
ANNUAL REVIEW OF BIOCHEMISTRY, VOL 80, 2011, 80 :247-271
[4]   Mass spectrometry of membrane transporters reveals subunit stoichiometry and interactions [J].
Barrera, Nelson P. ;
Isaacson, Shoshanna C. ;
Zhou, Min ;
Bavro, Vassiliy N. ;
Welch, Alex ;
Schaedler, Theresia A. ;
Seeger, Markus A. ;
Miguel, Ricardo Nunez ;
Korkhov, Vladimir M. ;
van Veen, Hendrik W. ;
Venter, Henrietta ;
Walmsley, Adrian R. ;
Tate, Christopher G. ;
Robinson, Carol V. .
NATURE METHODS, 2009, 6 (08) :585-U49
[5]   Self-assembly of discoidal phospholipid bilayer nanoparticles with membrane scaffold proteins [J].
Bayburt, TH ;
Grinkova, YV ;
Sligar, SG .
NANO LETTERS, 2002, 2 (08) :853-856
[6]   Different Modes of Lipid Binding to Membrane Proteins Probed by Mass Spectrometry [J].
Bechara, Cherine ;
Robinson, Carol V. .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2015, 137 (16) :5240-5247
[7]  
Bechara C, 2015, NAT CHEM, V7, P255, DOI [10.1038/nchem.2172, 10.1038/NCHEM.2172]
[8]  
BLIGH EG, 1959, CAN J BIOCHEM PHYS, V37, P911
[9]   SORTING OF GPI-ANCHORED PROTEINS TO GLYCOLIPID-ENRICHED MEMBRANE SUBDOMAINS DURING TRANSPORT TO THE APICAL CELL-SURFACE [J].
BROWN, DA ;
ROSE, JK .
CELL, 1992, 68 (03) :533-544
[10]   Quantitative analysis of biological membrane lipids at the low picomole level by nano-electrospray ionization tandem mass spectrometry [J].
Brugger, B ;
Erben, G ;
Sandhoff, R ;
Wieland, FT ;
Lehmann, WD .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (06) :2339-2344