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猴空泡病毒40 T抗原与猴空泡病毒40结合位点II的结合研究。

Binding studies of SV40 T-antigen to SV40 binding site II.

作者信息

Gottlieb P, Nasoff M S, Fisher E F, Walsh A M, Caruthers M H

出版信息

Nucleic Acids Res. 1985 Sep 25;13(18):6621-34. doi: 10.1093/nar/13.18.6621.

Abstract

SV40 T-Antigen binding site II was synthesized, cloned and analyzed for its ability to bind purified SV40 T-antigen. We report the binding constant of T-antigen for isolated site II. Using a filter binding assay the calculated binding constant was 6-8 fold less efficient than site I previously reported. Binding constants were calculated using two methods. The first was a direct calculation using a protein titration curve (KD). The second was by the ratio of measured association and dissociation rates. Both methods gave similar constants. Protection studies with SV40 T-antigen on the T-antigen binding sites in the wild-type array demonstrated that the binding constants of site I and site II are similar to those calculated for the individual sites. These results demonstrate that SV40 T-antigen does not bind cooperatively to sites one and two as earlier believed and are in agreement with recent observations emanating from several laboratories.

摘要

合成、克隆了SV40 T抗原结合位点II,并分析了其与纯化的SV40 T抗原的结合能力。我们报告了T抗原与分离的位点II的结合常数。使用滤膜结合试验,计算出的结合常数比先前报道的位点I效率低6至8倍。结合常数用两种方法计算。第一种是使用蛋白质滴定曲线直接计算(KD)。第二种是通过测量的缔合和解离速率之比。两种方法得到的常数相似。对野生型阵列中T抗原结合位点进行的SV40 T抗原保护研究表明,位点I和位点II的结合常数与为单个位点计算的常数相似。这些结果表明,SV40 T抗原并不像先前认为的那样与位点一和位点二协同结合,这与几个实验室最近的观察结果一致。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a38/321981/3ab17e8a253f/nar00312-0232-a.jpg

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