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使鸟嘌呤核苷酸结合功能丧失的ras基因产物p21的突变。

Mutations of the ras gene product p21 that abolish guanine nucleotide binding.

作者信息

Clanton D J, Hattori S, Shih T Y

出版信息

Proc Natl Acad Sci U S A. 1986 Jul;83(14):5076-80. doi: 10.1073/pnas.83.14.5076.

Abstract

We have constructed several point mutations affecting the GTP-binding site of p21, the ras-encoded protein. Both lysine (116K) and tyrosine (116Y) mutations of asparagine-116, which, by analogy with the crystal structure of elongation factor Tu (EF-Tu), has critical interactions with the guanine base, abolish GTP binding and transforming activities of p21. These activities are retained by proteins with a mutation at position 117 or 118. Both 116K and 116Y mutant p21s, when overproduced in Escherichia coli, are apparently devoid of GTP-binding and autokinase activities. Similarly, the mutant DNAs do not transform NIH 3T3 cells in a focus-forming assay. By cotransfection with pSV-neo, cell clones resistant to the neomycin analog G418 have been isolated. Cells transfected with 116K or 116Y mutant DNA are contact inhibited. In contrast to competent clones, the defective mutants have no detectable phosphorylated p21. The present results suggest that the basic structure of the GTP-binding site is conserved between p21 and EF-Tu and that this binding site is crucial for ras gene function.

摘要

我们构建了几个影响p21(ras编码蛋白)GTP结合位点的点突变。天冬酰胺-116的赖氨酸(116K)和酪氨酸(116Y)突变,通过与延伸因子Tu(EF-Tu)的晶体结构类比,该位点与鸟嘌呤碱基有关键相互作用,可消除p21的GTP结合和转化活性。在第117或118位发生突变的蛋白质保留了这些活性。当在大肠杆菌中过量表达时,116K和116Y突变型p21显然都没有GTP结合和自身激酶活性。同样,在焦点形成试验中,突变DNA不能转化NIH 3T3细胞。通过与pSV-neo共转染,分离出了对新霉素类似物G418有抗性的细胞克隆。用116K或116Y突变DNA转染的细胞受到接触抑制。与有能力的克隆不同,有缺陷的突变体没有可检测到的磷酸化p21。目前的结果表明,p21和EF-Tu之间GTP结合位点的基本结构是保守的,并且该结合位点对ras基因功能至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ced1/323893/db762ec99b49/pnas00318-0113-a.jpg

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