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B细胞的CD19作为替代激酶插入区域与磷脂酰肌醇3激酶结合。

CD19 of B cells as a surrogate kinase insert region to bind phosphatidylinositol 3-kinase.

作者信息

Tuveson D A, Carter R H, Soltoff S P, Fearon D T

机构信息

Department of Molecular Biology and Genetics, Johns Hopkins University School of Medicine, Baltimore, MD 21205.

出版信息

Science. 1993 May 14;260(5110):986-9. doi: 10.1126/science.7684160.

Abstract

Antigen receptors on B and T lymphocytes transduce signals by activating nonreceptor protein tyrosine kinases (PTKs). A family of receptor PTKs contains kinase insert regions with the sequence tyrosine-X-X-methionine (where X is any amino acid) that when phosphorylated mediate the binding and activation of phosphatidylinositol 3-kinase (PI 3-kinase). The CD19 membrane protein of B cells enhances activation through membrane immunoglobulin M (mIgM) and was found to contain a functional analog of the kinase insert region. Ligation of mIgM induced phosphorylation of CD19 and association with PI 3-kinase. Thus, CD19 serves as a surrogate kinase insert region for mIgM by providing the means for PI 3-kinase activation by nonreceptor PTKs.

摘要

B淋巴细胞和T淋巴细胞上的抗原受体通过激活非受体蛋白酪氨酸激酶(PTK)来转导信号。一类受体PTK含有激酶插入区域,其序列为酪氨酸-X-X-甲硫氨酸(其中X为任意氨基酸),磷酸化后可介导磷脂酰肌醇3激酶(PI 3激酶)的结合与激活。B细胞的CD19膜蛋白通过膜免疫球蛋白M(mIgM)增强激活作用,并且发现其含有激酶插入区域的功能类似物。mIgM的连接诱导CD19磷酸化并与PI 3激酶结合。因此,CD19通过提供非受体PTK激活PI 3激酶的方式,作为mIgM的替代激酶插入区域。

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