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鉴定GIYWHHY作为人p60c-src蛋白酪氨酸激酶的一种新型肽底物。

Identification of GIYWHHY as a novel peptide substrate for human p60c-src protein tyrosine kinase.

作者信息

Lou Q, Leftwich M E, Lam K S

机构信息

Arizona Cancer Center, Tucson, USA.

出版信息

Bioorg Med Chem. 1996 May;4(5):677-82. doi: 10.1016/0968-0896(96)00063-6.

Abstract

We have recently determined that -Ile-Tyr- were the two critical residues as a peptide substrate for p60c-src protein tyrosine kinase (Lou, Q. et al., Lett. Peptide Sci., 1995, 2, 289). Here, we report on the design and synthesis of a secondary 'one-bead, one-compound' combinatorial peptide library based on this dipeptide motif (XIYXXXX, where X = all 19 eukaryotic amino acids except for cysteine). This secondary library was screened for its ability to be phosphorylated by p60c-src PTK using [gamma 32P]ATP as a tracer. Five of the strongest [32P]-labeled peptide-beads were identified and microsequenced: GIYWHHY, KIYDDYE, EIYEENG, EIYEEYE, and YIYEEED. A solid-phase phosphorylation assay was used to evaluate the structure-activity relationship of GIYWHHY. It was determined that Ile2, Tyr3, His5, and His6 were crucial for its activity as a substrate.

摘要

我们最近确定,-Ile-Tyr-是作为p60c-src蛋白酪氨酸激酶的肽底物的两个关键残基(Lou, Q.等人,《肽科学快报》,1995年,2卷,289页)。在此,我们报告基于此二肽基序(XIYXXXX,其中X = 除半胱氨酸外的所有19种真核氨基酸)设计和合成的第二代“单珠单化合物”组合肽库。使用[γ-32P]ATP作为示踪剂,筛选该第二代文库被p60c-src PTK磷酸化的能力。鉴定出五个放射性最强的[32P]标记的肽珠并进行微量测序:GIYWHHY、KIYDDYE、EIYEENG、EIYEEYE和YIYEEED。采用固相磷酸化试验评估GIYWHHY的构效关系。确定Ile2、Tyr3、His5和His6对其作为底物的活性至关重要。

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