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Itk/Tsk Src同源结构域3配体的鉴定。

Identification of Itk/Tsk Src homology 3 domain ligands.

作者信息

Bunnell S C, Henry P A, Kolluri R, Kirchhausen T, Rickles R J, Berg L J

机构信息

Department of Molecular and Cellular Biology, Harvard University, Cambridge, Massachusetts 02138, USA.

出版信息

J Biol Chem. 1996 Oct 11;271(41):25646-56. doi: 10.1074/jbc.271.41.25646.

Abstract

The tyrosine kinase Itk/Tsk is a T cell specific analog of Btk, the tyrosine kinase defective in the human immunodeficiency X-linked agammaglobulinemia and in xid mice. T lymphocytes from Itk-deficient mice are refractory to mitogenic stimuli delivered through the T cell receptor (TCR). To gain insights into the biochemical role of Itk, the binding properties of the Itk SH3 domain were examined. An optimal Itk SH3 binding motif was derived by screening biased phage display libraries; peptides based on this motif bound with high affinity and selectivity to the Itk SH3 domain. Initial studies with T cell lysates indicated that the Itk SH3 domain bound Cbl, Fyn, and other tyrosine phosphoproteins from TCR-stimulated Jurkat cells. Under conditions of increased detergent stringency Sam 68, Wiskott-Aldrich Syndrome protein, and hnRNP-K, but not Cbl and Fyn, were bound to the Itk SH3 domain. By examining the ability of different SH3 domains to interact with deletion variants of Sam 68 and WASP, we demonstrated that the Itk-SH3 domain and the SH3 domains of Src family kinases bind to overlapping but distinct sets of proline-rich regions in Sam 68 and WASP.

摘要

酪氨酸激酶Itk/Tsk是Btk的T细胞特异性类似物,Btk是人类免疫缺陷X连锁无丙种球蛋白血症和xid小鼠中存在缺陷的酪氨酸激酶。来自Itk缺陷小鼠的T淋巴细胞对通过T细胞受体(TCR)传递的促有丝分裂刺激具有抗性。为了深入了解Itk的生化作用,我们研究了Itk SH3结构域的结合特性。通过筛选偏向性噬菌体展示文库获得了最佳的Itk SH3结合基序;基于该基序的肽与Itk SH3结构域具有高亲和力和选择性结合。对T细胞裂解物的初步研究表明,Itk SH3结构域与来自TCR刺激的Jurkat细胞的Cbl、Fyn和其他酪氨酸磷酸化蛋白结合。在去污剂严格度增加的条件下,Sam 68、威斯科特-奥尔德里奇综合征蛋白和hnRNP-K与Itk SH3结构域结合,但Cbl和Fyn不与Itk SH3结构域结合。通过研究不同SH3结构域与Sam 68和WASP缺失变体相互作用的能力,我们证明了Itk-SH结构域和Src家族激酶的SH3结构域与Sam 68和WASP中富含脯氨酸区域的重叠但不同的集合结合。

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