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定点突变使兔钙环蛋白形成二聚体。

Site-directed mutation makes rabbit calcyclin dimer.

作者信息

Ando Y, Watanabe M, Akatsuka H, Tokumitsu H, Hidaka H

机构信息

Department of Pharmacology, Nagoya University School of Medicine, Japan.

出版信息

FEBS Lett. 1992 Dec 14;314(2):109-13. doi: 10.1016/0014-5793(92)80953-e.

Abstract

Unlike human, rat and mouse calcyclin, purified rabbit calcyclin did not form a dimer on Tricine SDS-PAGE under non-reduced conditions. Based on the internal peptide sequence of rabbit calcylin, we isolated and sequenced a cDNA clone encoding calcyclin. The sequence of this clone (pCalC) is 629 bp long and codes 90 amino acid residues of a protein with a molecular mass of 10,153 Da. By Northern blot analysis, a major band of 0.9 kbp and a minor band of 2.6 kbp were detected in the lung. The recombinant calcyclin mutated serine at the third position to cysteine was expressed in E. coli and made dimer formation under non-reduced conditions on SDS-PAGE. Whether or not this type of mutation which prevents dimer formation of calcyclin plays a physiological role in the rabbit lung is the subject of an ongoing study.

摘要

与人和大鼠及小鼠的钙结合蛋白不同,纯化后的兔钙结合蛋白在非还原条件下的Tricine SDS-PAGE上不会形成二聚体。基于兔钙结合蛋白的内部肽序列,我们分离并测序了一个编码钙结合蛋白的cDNA克隆。该克隆(pCalC)的序列长629 bp,编码一个分子量为10153 Da的蛋白质的90个氨基酸残基。通过Northern印迹分析,在肺中检测到一条0.9 kbp的主要条带和一条2.6 kbp的次要条带。将重组钙结合蛋白第三位的丝氨酸突变为半胱氨酸,在大肠杆菌中表达,并在非还原条件下的SDS-PAGE上形成二聚体。这种阻止钙结合蛋白二聚体形成的突变类型在兔肺中是否发挥生理作用是一项正在进行的研究课题。

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