Proliferating cell nuclear antigen loaded onto double-stranded DNA: dynamics, minor groove interactions and functional implications

被引:62
|
作者
Ivanov, Ivaylo
Chapados, Brian R.
McCammon, J. Andrew
Tainer, John A.
机构
[1] Univ Calif San Diego, Dept Chem & Biochem, Dept Pharmacol, Howard Hughes Med Inst, La Jolla, CA 92093 USA
[2] Univ Calif San Diego, Ctr Theoret Biol Phys, La Jolla, CA 92093 USA
[3] Scripps Res Inst, Dept Biol Mol, La Jolla, CA 92037 USA
[4] Scripps Res Inst, Skaggs Inst Chem Biol, La Jolla, CA 92037 USA
[5] Lawrence Berkeley Natl Lab, Life Sci Div, Dept Biol Mol, Berkeley, CA 94720 USA
关键词
D O I
10.1093/nar/gkl744
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) acts as a biologically essential processivity factor that encircles DNA and provides binding sites for polymerase, flap endonuclease-1 (FEN-1) and ligase during DNA replication and repair. We have computationally characterized the interactions of human and Archaeoglobus fulgidus PCNA trimer with double-stranded DNA (ds DNA) using multi-nanosecond classical molecular dynamics simulations. The results reveal the interactions of DNA passing through the PCNA trimeric ring including the contacts formed, overall orientation and motion with respect to the sliding clamp. Notably, we observe pronounced tilting of the axis of dsDNA with respect to the PCNA ring plane reflecting interactions between the DNA phosphodiester backbone and positively charged arginine and lysine residues lining the PCNA inner surface. Covariance matrix analysis revealed a pattern of correlated motions within and between the three equivalent subunits involving the PCNA C-terminal region and linker strand associated with partner protein binding sites. Additionally, principal component analysis identified low frequency global PCNA subunit motions suitable for translocation along duplex DNA. The PCNA motions and interactions with the DNA minor groove, identified here computationally, provide an unexpected basis for PCNA to act in the coordinated handoff of intermediates from polymerase to FEN-1 to ligase during DNA replication and repair.
引用
收藏
页码:6023 / 6033
页数:11
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