Chen J, Peters R, Saha P, Lee P, Theodoras A, Pagano M, Wagner G, Dutta A
Department of Pathology, Division of Molecular Oncology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115, USA.
Nucleic Acids Res. 1996 May 1;24(9):1727-33. doi: 10.1093/nar/24.9.1727.
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.
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。