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A proteomics approach to identify proliferating cell nuclear antigen (PCNA)-binding proteins in human cell lysates - Identification of the human CHL12/RFCs2-5 complex as a novel PCNA-binding protein
被引:78
作者:
Ohta, S
Shiomi, Y
Sugimoto, K
Obuse, C
Tsurimoto, T
[1
]
机构:
[1] Nara Inst Sci & Technol, Nara 6300101, Japan
[2] Nagoya Univ, Grad Sch Sci, Div Biol Sci, Chikusa Ku, Nagoya, Aichi 4640814, Japan
关键词:
D O I:
10.1074/jbc.M206194200
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:
Proliferating cell nuclear antigen (PCNA), a eukaryotic DNA replication factor, functions not only as a processivity factor for DNA polymerase 5 but also as a binding partner for multiple other factors. To understand its broad significance, we have carried out systematic studies of PCNA-binding proteins by a combination of affinity chromatography and mass spectrometric analyses. We detected more than 20 specific protein bands of various intensities in fractions bound to PCNA-fixed resin from human cell lysates and determined their peptide sequences by liquid chromatography and tandem mass spectrometry. A search with human protein data bases identified 12 reported PCNA-binding proteins from both cytoplasmic (S100 lysate) and nuclear extracts with substantial significance and four more solely from the nuclear preparation. CHL12, a factor involved in checkpoint response and chromosome cohesion, was a novel example found in both lysates. Further studies with recombinant proteins demonstrated that CHL12 and small subunits of replication factor C form a complex that interacts with PCNA.
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页码:40362 / 40367
页数:6
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