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Protein-nucleic acid complexes and the role of mass spectrometry in their structure determination
被引:12
作者:
Park, Ah Young
[1
]
Robinson, Carol V.
[1
]
机构:
[1] Univ Oxford, Dept Chem, Oxford OX1 3QZ, England
基金:
英国生物技术与生命科学研究理事会;
关键词:
Mass spectrometry;
ion-mobility mass spectrometry;
collision cross section;
structural biology;
hybrid structure determination;
RNA-POLYMERASE-III;
BINDING ATTENUATION PROTEIN;
TRANSLATION FACTOR EIF3;
ION MOBILITY;
TRANSCRIPTION INITIATION;
SUBUNIT ARCHITECTURE;
CLAMP LOADER;
MACROMOLECULAR ASSEMBLIES;
ACCESSORY PROTEINS;
CRYSTAL-STRUCTURE;
D O I:
10.3109/10409238.2011.559451
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:
Mass spectrometry is now established as a powerful tool for the study of the stoichiometry, interactions, dynamics, and subunit architecture of large protein assemblies and their subcomplexes. Recent evidence has suggested that the 3D structure of protein complexes can be maintained intact in the gas phase, highlighting the potential of ion mobility to contribute to structural biology. A key challenge is to integrate the compositional and structural information from ion mobility mass spectrometry with molecular modelling approaches to produce 3D models of intact protein complexes. In this review, we focus on the mass spectrometry of protein-nucleic acid assemblies with particular attention to the application of ion mobility, an emerging technique in structural studies. We also discuss the challenges that lie ahead for the full integration of ion mobility mass spectrometry with structural biology.
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页码:152 / 164
页数:13
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