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Photodissociation and Dissociative Photoionization Mass Spectrometry of Proteins and Noncovalent Protein-Ligand Complexes
被引:42
作者:

Canon, Francis
论文数: 0 引用数: 0
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机构:
Synchrotron SOLEIL, F-91192 Gif Sur Yvette, France
INRA, UMR1324, Ctr Sci Gout & Alimentat, F-21065 Dijon, France Synchrotron SOLEIL, F-91192 Gif Sur Yvette, France

Milosavljevic, Aleksandar R.
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Belgrade, Inst Phys Belgrade, Belgrade 11080, Serbia Synchrotron SOLEIL, F-91192 Gif Sur Yvette, France

论文数: 引用数:
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Refregiers, Matthieu
论文数: 0 引用数: 0
h-index: 0
机构:
Synchrotron SOLEIL, F-91192 Gif Sur Yvette, France Synchrotron SOLEIL, F-91192 Gif Sur Yvette, France

Nahon, Laurent
论文数: 0 引用数: 0
h-index: 0
机构:
Synchrotron SOLEIL, F-91192 Gif Sur Yvette, France Synchrotron SOLEIL, F-91192 Gif Sur Yvette, France

Sarni-Manchado, Pascale
论文数: 0 引用数: 0
h-index: 0
机构:
INRA, Sci Oenol UMR1083, F-34060 Montpellier, France Synchrotron SOLEIL, F-91192 Gif Sur Yvette, France

Cheynier, Veronique
论文数: 0 引用数: 0
h-index: 0
机构:
INRA, Sci Oenol UMR1083, F-34060 Montpellier, France Synchrotron SOLEIL, F-91192 Gif Sur Yvette, France

Giuliani, Alexandre
论文数: 0 引用数: 0
h-index: 0
机构:
Synchrotron SOLEIL, F-91192 Gif Sur Yvette, France
INRA, CEPIA, UAR1008, F-44316 Nantes, France Synchrotron SOLEIL, F-91192 Gif Sur Yvette, France
机构:
[1] Synchrotron SOLEIL, F-91192 Gif Sur Yvette, France
[2] INRA, UMR1324, Ctr Sci Gout & Alimentat, F-21065 Dijon, France
[3] INRA, CEPIA, UAR1008, F-44316 Nantes, France
[4] Univ Belgrade, Inst Phys Belgrade, Belgrade 11080, Serbia
[5] INRA, Sci Oenol UMR1083, F-34060 Montpellier, France
[6] Univ Paris 11, Lab Chim Phys, F-91405 Orsay, France
关键词:
dissociative photoionization;
mass spectrometry;
proteins;
tannins;
VUV photon activation;
PROLINE-RICH PROTEIN;
TOP-DOWN PROTEOMICS;
SYNCHROTRON-RADIATION;
PEPTIDES;
TANNINS;
BINDING;
NM;
D O I:
10.1002/anie.201304046
中图分类号:
O6 [化学];
学科分类号:
0703 ;
摘要:
Weight of evidence: Using synchrotron radiation, photo-fragmentation of an intrinsically disordered protein is probed and compared with classical tandem mass-spectrometry activation techniques. It provides excellent sequence coverage allowing the identification of the protein noncovalent binding sites. Copyright © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
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页码:8377 / 8381
页数:5
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