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SPARC与内皮细胞的特异性相互作用是通过一个包含钙结合EF手的羧基末端序列介导的。

Specific interaction of SPARC with endothelial cells is mediated through a carboxyl-terminal sequence containing a calcium-binding EF hand.

作者信息

Yost J C, Sage E H

机构信息

Department of Biological Structure, University of Washington, Seattle 98195.

出版信息

J Biol Chem. 1993 Dec 5;268(34):25790-6.

PMID:8245016
Abstract

SPARC is a secreted, Ca(2+)-binding protein that modulates cell shape and gene expression (Sage, E.H., and Bornstein, P. (1991) J. Biol. Chem. 266, 14831-14834). In the present study we questioned whether SPARC interacted with an endothelial cell surface receptor. The binding of 125I-SPARC to bovine aortic endothelial cells was dependent on Ca2+ and was sensitive to small changes in extracellular pH; maximal binding occurred at pH 7.1. Scatchard analysis indicated approximately 2.3 x 10(7) binding sites/cell with an apparent KI of 1.1 nM. The interaction was diminished specifically by competition with synthetic peptides corresponding to amino acids 54-73 (SPARC 54-73) and 254-273 (SPARC254-273). The binding of 125I-SPARC254-273, a sequence containing a Ca(2+)-binding EF-hand, was saturated within 45 min at a concentration of 5 microM; Scatchard analysis indicated 4.2 x 10(7) sites/cell and a KI of 2.4 nM. Iodinated proteins from plasma membranes were affinity-chromatographed on SPARC254-273; several proteins with apparent masses ranging from 153 to 100 kDa (unreduced) or from 153 to 122 kDa (reduced) were eluted with the soluble peptide. These proteins represent candidates for a SPARC receptor(s) that mediates the biological activity of this protein on endothelial cells.

摘要

SPARC是一种分泌型的、能结合钙离子的蛋白质,可调节细胞形态和基因表达(塞奇,E.H.,和伯恩斯坦,P.(1991年)《生物化学杂志》266卷,14831 - 14834页)。在本研究中,我们探究了SPARC是否与内皮细胞表面受体相互作用。125I - SPARC与牛主动脉内皮细胞的结合依赖于钙离子,并且对细胞外pH值的微小变化敏感;最大结合发生在pH 7.1时。斯卡查德分析表明,每个细胞大约有2.3×10^7个结合位点,表观解离常数为1.1 nM。通过与对应于氨基酸54 - 73(SPARC 54 - 73)和254 - 273(SPARC254 - 273)的合成肽竞争,这种相互作用会特异性减弱。125I - SPARC254 - 273(一个包含钙离子结合EF手结构的序列)在5 microM浓度下45分钟内达到饱和结合;斯卡查德分析表明每个细胞有4.2×10^7个位点,解离常数为2.4 nM。来自质膜的碘化蛋白在SPARC254 - 273上进行亲和层析;几种表观分子量在153至100 kDa(未还原)或153至122 kDa(还原)范围内的蛋白质与可溶性肽一起被洗脱。这些蛋白质代表了介导该蛋白在内皮细胞上生物活性的SPARC受体的候选者。

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