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一种中心体蛋白FOR20作为新型S100A6靶点的鉴定与表征

Identification and characterization of a centrosomal protein, FOR20 as a novel S100A6 target.

作者信息

Sakane Kyohei, Nishiguchi Miyu, Denda Miwako, Yamagchi Fuminori, Magari Masaki, Kanayama Naoki, Morishita Ryo, Tokumitsu Hiroshi

机构信息

Division of Medical Bioengineering, Graduate School of Natural Science and Technology, Okayama University, Okayama 700-8530, Japan.

Department of Applied Chemistry and Biotechnology, Faculty of Engineering, Okayama University, Okayama 700-8530, Japan.

出版信息

Biochem Biophys Res Commun. 2017 Sep 30;491(4):980-985. doi: 10.1016/j.bbrc.2017.07.161. Epub 2017 Jul 29.

Abstract

S100A6 is a Ca-signal transducer that interacts with numerous proteins and regulates their biochemical functions. Here we identified a centrosomal protein, FOR20 (FOP-related protein of 20 kDa) as a novel S100A6 target by screening protein microarrays carrying 19,676 recombinant GST-fused human proteins. Binding experiments revealed that S100A6 interacts with the N-terminal region (residues 1-30) of FOR20 in a Ca-dependent manner in vitro and in living cells. Several S100 proteins including S100A1, A2, A4, A11, B also exhibited Ca-dependent interactions with FOR20 as well as S100A6. We found that two distantly related centrosomal proteins, FOP and OFD1, also possess N-terminal regions with a significant sequence similarity to the putative S100A6-binding site (residues 1-30) in FOR20 and are capable of binding to S100A6 in a Ca-dependent manner. Taken together, these results may indicate that S100A6 interacts with FOR20 and related centrosomal proteins through a conserved N-terminal domain, suggesting a novel Ca-dependent regulation of centrosomal function.

摘要

S100A6是一种钙信号转导蛋白,可与多种蛋白质相互作用并调节其生化功能。在此,我们通过筛选携带19,676种重组GST融合人蛋白的蛋白质微阵列,鉴定出一种中心体蛋白FOR20(20 kDa的FOP相关蛋白)为新型S100A6靶点。结合实验表明,S100A6在体外和活细胞中以钙依赖的方式与FOR20的N端区域(第1 - 30位氨基酸残基)相互作用。包括S100A1、A2、A4、A11、B在内的几种S100蛋白也表现出与FOR20以及S100A6的钙依赖相互作用。我们发现,两种远缘相关的中心体蛋白FOP和OFD1,其N端区域与FOR20中假定的S100A6结合位点(第1 - 30位氨基酸残基)具有显著的序列相似性,并且能够以钙依赖的方式与S100A6结合。综上所述,这些结果可能表明S100A6通过保守的N端结构域与FOR20及相关中心体蛋白相互作用,提示了一种新型的钙依赖的中心体功能调节机制。

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