The emerging role of native mass spectrometry in characterizing the structure and dynamics of macromolecular complexes

Protein Science

Volumn 24, Issue 8, 2015, Pages 1176-1192

  Erba, Elisabetta Boeri ^a,b   Petosa, Carlo ^a,b  

^a UNIV GRENOBLE ALPES   (France)

^b INSTITUT DE BIOLOGIE STRUCTURALE   (France)

Author keywords

2D interaction map; Macromolecular complexes; Native mass spectrometry (MS); Protein2ligand interactions; Stoichiometry; Top down MS

Indexed keywords

KELCH LIKE ECH ASSOCIATED PROTEIN 1; MEMBRANE PROTEIN; LIGAND; MACROMOLECULE; PROTEIN;

ARTICLE; ATOMIC FORCE MICROSCOPY; COLLISIONALLY ACTIVATED DISSOCIATION; COVALENT BOND; DEUTERIUM HYDROGEN EXCHANGE; DISSOCIATION; ELECTROSPRAY; ELECTROSPRAY MASS SPECTROMETRY; FOURIER TRANSFORMATION; HUMAN; LIQUID CHROMATOGRAPHY; MACROMOLECULE; MASS SPECTROMETRY; MATRIX ASSISTED LASER DESORPTION IONIZATION TIME OF FLIGHT MASS SPECTROMETRY; PRIORITY JOURNAL; PROTEIN CONFORMATION; PROTEIN INTERACTION; PROTEIN QUATERNARY STRUCTURE; RELATIVE BINDING AFFINITY; STOICHIOMETRY; SURFACE PLASMON RESONANCE; X RAY CRYSTALLOGRAPHY; ANIMAL; CHEMICAL STRUCTURE; CHEMISTRY; DEVICES; FOURIER ANALYSIS; METABOLISM; PROCEDURES;

ANIMALS; FOURIER ANALYSIS; HUMANS; LIGANDS; MACROMOLECULAR SUBSTANCES; MASS SPECTROMETRY; MEMBRANE PROTEINS; MODELS, MOLECULAR; PROTEIN CONFORMATION; PROTEINS;

EID: 84943407635     PISSN: 09618368     EISSN: 1469896X     Source Type: Journal    
DOI: 10.1002/pro.2661     Document Type: Article

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