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细胞周期调节因子p21的一个39个氨基酸的片段足以结合增殖细胞核抗原并在体内部分抑制DNA复制。

A 39 amino acid fragment of the cell cycle regulator p21 is sufficient to bind PCNA and partially inhibit DNA replication in vivo.

作者信息

Chen J, Peters R, Saha P, Lee P, Theodoras A, Pagano M, Wagner G, Dutta A

机构信息

Department of Pathology, Division of Molecular Oncology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115, USA.

出版信息

Nucleic Acids Res. 1996 May 1;24(9):1727-33. doi: 10.1093/nar/24.9.1727.

Abstract

The cell cycle regulator p21 interacts with and inhibits the DNA replication and repair factor proliferating cell nuclear antigen (PCNA). We have defined a 39 amino acid fragment of p21 which is sufficient to bind PCNA with high affinity (Kd 10-20 nM). This peptide can inhibit DNA replication in vitro and microinjection of a GST fusion protein containing this domain inhibited S phase in vivo. Despite its high affinity for PCNA, the free 39 amino acid peptide does not have a well-defined structure, as judged from circular dichroism and nuclear magnetic resonance measurements, suggesting an induced fit mechanism for the PCNA-p21 interaction. The association of the small peptide with PCNA was thermolabile, suggesting that portions of p21 adjoining the minimal region of contact stabilize the interaction. In addition, a domain containing 67 amino acids from the N-terminus of PCNA was defined as both necessary and sufficient for binding to p21.

摘要

细胞周期调节因子p21与DNA复制及修复因子增殖细胞核抗原(PCNA)相互作用并对其产生抑制作用。我们已确定p21的一个39个氨基酸的片段,该片段足以与PCNA高亲和力结合(解离常数Kd为10 - 20 nM)。此肽段可在体外抑制DNA复制,且显微注射含有该结构域的GST融合蛋白可在体内抑制S期。尽管其对PCNA具有高亲和力,但根据圆二色性和核磁共振测量判断,游离的39个氨基酸肽段并没有明确的结构,这表明PCNA与p21的相互作用存在诱导契合机制。小肽与PCNA的结合对热不稳定,这表明p21中与最小接触区域相邻的部分可稳定这种相互作用。此外,PCNA N端的一个包含67个氨基酸的结构域被确定为与p21结合既必要又充分。

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