Literature DB >> 32020797

Native Mass Spectrometry: What is in the Name?

Aneika C Leney1,2, Albert J R Heck1,2.   

Abstract

Electrospray ionization mass spectrometry (ESI-MS) is nowadays one of the cornerstones of biomolecular mass spectrometry and proteomics. Advances in sample preparation and mass analyzers have enabled researchers to extract much more information from biological samples than just the molecular weight. In particular, relevant for structural biology, noncovalent protein-protein and protein-ligand complexes can now also be analyzed by MS. For these types of analyses, assemblies need to be retained in their native quaternary state in the gas phase. This initial small niche of biomolecular mass spectrometry, nowadays often referred to as "native MS," has come to maturation over the last two decades, with dozens of laboratories using it to study mostly protein assemblies, but also DNA and RNA-protein assemblies, with the goal to define structure-function relationships. In this perspective, we describe the origins of and (re)define the term native MS, portraying in detail what we meant by "native MS," when the term was coined and also describing what it does (according to us) not entail. Additionally, we describe a few examples highlighting what native MS is, showing its successes to date while illustrating the wide scope this technology has in solving complex biological questions.

Keywords:  Electrospray ionization mass spectrometry (ESI-MS); Native mass spectrometry

Year:  2017        PMID: 32020797     DOI: 10.1021/jasms.8b05378

Source DB:  PubMed          Journal:  J Am Soc Mass Spectrom        ISSN: 1044-0305            Impact factor:   3.109


  62 in total

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3.  First-Principles Collision Cross Section Measurements of Large Proteins and Protein Complexes.

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Journal:  Anal Chem       Date:  2020-07-28       Impact factor: 6.986

4.  Structural Analysis of the Effect of a Dual-FLAG Tag on Transthyretin.

Authors:  Mehdi Shirzadeh; Michael L Poltash; Arthur Laganowsky; David H Russell
Journal:  Biochemistry       Date:  2020-03-02       Impact factor: 3.162

5.  Ultraviolet Photodissociation Mass Spectrometry for Analysis of Biological Molecules.

Authors:  Jennifer S Brodbelt; Lindsay J Morrison; Inês Santos
Journal:  Chem Rev       Date:  2019-12-18       Impact factor: 60.622

6.  Characterization of [2Fe-2S]-Cluster-Bridged Protein Complexes and Reaction Intermediates by use of Native Mass Spectrometric Methods.

Authors:  Mengxuan Jia; Sambuddha Sen; Christine Wachnowsky; Insiya Fidai; James A Cowan; Vicki H Wysocki
Journal:  Angew Chem Int Ed Engl       Date:  2020-03-03       Impact factor: 15.336

Review 7.  Mass Spectrometry-Based Protein Footprinting for Higher-Order Structure Analysis: Fundamentals and Applications.

Authors:  Xiaoran Roger Liu; Mengru Mira Zhang; Michael L Gross
Journal:  Chem Rev       Date:  2020-04-22       Impact factor: 60.622

8.  High Mass Analysis with a Fourier Transform Ion Cyclotron Resonance Mass Spectrometer: From Inorganic Salt Clusters to Antibody Conjugates and Beyond.

Authors:  Iain D G Campuzano; Michael Nshanian; Christopher Spahr; Carter Lantz; Chawita Netirojjanakul; Huilin Li; Piriya Wongkongkathep; Jeremy J Wolff; Joseph A Loo
Journal:  J Am Soc Mass Spectrom       Date:  2020-04-02       Impact factor: 3.109

9.  Uniting Native Capillary Electrophoresis and Multistage Ultraviolet Photodissociation Mass Spectrometry for Online Separation and Characterization of Escherichia coli Ribosomal Proteins and Protein Complexes.

Authors:  M Rachel Mehaffey; Qiangwei Xia; Jennifer S Brodbelt
Journal:  Anal Chem       Date:  2020-11-06       Impact factor: 6.986

10.  Collision-Induced Unfolding Studies of Proteins and Protein Complexes using Drift Tube Ion Mobility-Mass Spectrometer.

Authors:  Xueyun Zheng; Ruwan T Kurulugama; Arthur Laganowsky; David H Russell
Journal:  Anal Chem       Date:  2020-05-08       Impact factor: 6.986

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