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Pdx1同源结构域识别DNA时诱导契合机制的结构基础。

Structural basis for induced fit mechanisms in DNA recognition by the Pdx1 homeodomain.

作者信息

Longo Antonella, Guanga Gerald P, Rose Robert B

机构信息

Department of Molecular and Structural Biochemistry, 128 Polk Hall, North Carolina State University, Raleigh, North Carolina 27695, USA.

出版信息

Biochemistry. 2007 Mar 20;46(11):2948-57. doi: 10.1021/bi060969l. Epub 2007 Feb 23.

Abstract

Pancreatic and duodenal homeobox 1 (Pdx1) is a homeodomain transcription factor belonging to the ParaHox family. Pdx1 plays an essential role in pancreatic endocrine and exocrine cell development and maintenance of adult islet beta-cell function. Mutations in the human pdx1 gene are linked to an early onset form of non-insulin-dependent diabetes mellitus, MODY-4. We demonstrate that the homeodomain reproduces the binding specificity of the full-length protein. We report the 2.4 A resolution crystal structure of the homeodomain bound to a target DNA. The two Pdx1/DNA complexes in the asymmetric unit display conformational differences: in the DNA curvature, the orientation of the homeodomain in the major groove, and the order of the N-terminal arm. Comparing the two complexes indicates invariant protein-DNA contacts, and variant contacts that are unique to each binding orientation. An induced fit model is proposed that depends on the DNA conformation and provides a mechanism for nonlocal contributions to binding specificity.

摘要

胰腺十二指肠同源盒1(Pdx1)是一种属于副同源盒家族的同源结构域转录因子。Pdx1在胰腺内分泌和外分泌细胞发育以及成年胰岛β细胞功能维持中发挥着至关重要的作用。人类pdx1基因突变与非胰岛素依赖型糖尿病的早发型MODY-4相关。我们证明同源结构域再现了全长蛋白的结合特异性。我们报道了与靶DNA结合的同源结构域的2.4埃分辨率晶体结构。不对称单元中的两个Pdx1/DNA复合物表现出构象差异:在DNA曲率、同源结构域在大沟中的方向以及N端臂的顺序方面。比较这两个复合物表明存在不变的蛋白质-DNA接触以及每个结合方向特有的可变接触。提出了一种诱导契合模型,该模型取决于DNA构象,并为结合特异性的非局部贡献提供了一种机制。

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