High-Resolution Native Mass Spectrometry

被引:287
作者
Tamara, Sem [1 ,2 ,3 ]
den Boer, Maurits A. [1 ,2 ,3 ]
Heck, Albert J. R. [1 ,2 ,3 ]
机构
[1] Univ Utrecht, Biomol Mass Spectrometry & Prote, Bijvoet Ctr Biomol Res, NL-3584 CH Utrecht, Netherlands
[2] Univ Utrecht, Utrecht Inst Pharmaceut Sci, NL-3584 CH Utrecht, Netherlands
[3] Netherlands Prote Ctr, NL-3584 CH Utrecht, Netherlands
关键词
TIME-OF-FLIGHT; NONCOVALENT PROTEIN COMPLEXES; ELECTRON-TRANSFER DISSOCIATION; SURFACE-INDUCED DISSOCIATION; TOP-DOWN PROTEOMICS; RECEPTOR-LIGAND COMPLEXES; GAS-PHASE DISSOCIATION; NANOSCALE ION EMITTERS; DE-NOVO DESIGN; FOURIER-TRANSFORM;
D O I
10.1021/acs.chemrev.1c00212
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Native mass spectrometry (MS) involves the analysis and characterization of macromolecules, predominantly intact proteins and protein complexes, whereby as much as possible the native structural features of the analytes are retained. As such, native MS enables the study of secondary, tertiary, and even quaternary structure of proteins and other biomolecules. Native MS represents a relatively recent addition to the analytical toolbox of mass spectrometry and has over the past decade experienced immense growth, especially in enhancing sensitivity and resolving power but also in ease of use. With the advent of dedicated mass analyzers, sample preparation and separation approaches, targeted fragmentation techniques, and software solutions, the number of practitioners and novel applications has risen in both academia and industry. This review focuses on recent developments, particularly in high-resolution native MS, describing applications in the structural analysis of protein assemblies, proteoform profiling of-among others-biopharmaceuticals and plasma proteins, and quantitative and qualitative analysis of protein-ligand interactions, with the latter covering lipid, drug, and carbohydrate molecules, to name a few.
引用
收藏
页码:7269 / 7326
页数:58
相关论文
共 498 条
[1]   Mass Analysis of Macro-molecular Analytes via Multiply-Charged Ion Attachment [J].
Abdillahi, Abdirahman M. ;
Lee, Kenneth W. ;
McLuckey, Scott A. .
ANALYTICAL CHEMISTRY, 2020, 92 (24) :16301-16306
[2]   Mass-spectrometric exploration of proteome structure and function [J].
Aebersold, Ruedi ;
Mann, Matthias .
NATURE, 2016, 537 (7620) :347-355
[3]   How paired PSII-LHCII supercomplexes mediate the stacking of plant thylakoid membranes unveiled by structural mass-spectrometry [J].
Albanese, Pascal ;
Tamara, Sem ;
Saracco, Guido ;
Scheltema, Richard A. ;
Pagliano, Cristina .
NATURE COMMUNICATIONS, 2020, 11 (01)
[4]   Single-Molecule Analysis with Solid-State Nanopores [J].
Albrecht, Tim .
ANNUAL REVIEW OF ANALYTICAL CHEMISTRY, VOL 12, 2019, 12 :371-387
[5]   High-sensitivity Analytical Approaches for the Structural Characterization of Glycoproteins [J].
Alley, William R., Jr. ;
Mann, Benjamin F. ;
Novotny, Milos V. .
CHEMICAL REVIEWS, 2013, 113 (04) :2668-2732
[6]  
Allison T. M., 2019, ADV ION MOBILITY MAS, V83, P161
[7]   Next-generation proteomics: towards an integrative view of proteome dynamics [J].
Altelaar, A. F. Maarten ;
Munoz, Javier ;
Heck, Albert J. R. .
NATURE REVIEWS GENETICS, 2013, 14 (01) :35-48
[8]   Antibody glycosylation in inflammation, disease and vaccination [J].
Alter, Galit ;
Ottenhoff, Tom H. M. ;
Joosten, Simone A. .
SEMINARS IN IMMUNOLOGY, 2018, 39 (0C) :102-110
[9]   The Clinical Plasma Proteome: A Survey of Clinical Assays for Proteins in Plasma and Serum [J].
Anderson, N. Leigh .
CLINICAL CHEMISTRY, 2010, 56 (02) :177-185
[10]   The smaller the better [J].
不详 .
NATURE METHODS, 2008, 5 (06) :457-457