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参与限制性内切酶EcoRI切割DNA过程的多肽序列。

Polypeptide sequences involved in the cleavage of DNA by the restriction endonuclease EcoRI.

作者信息

Scholtissek S, Pingoud A, Maass G, Zabeau M

出版信息

J Biol Chem. 1986 Feb 15;261(5):2228-34.

PMID:3003104
Abstract

We have prepared a variety of fragments of the restriction endonuclease EcoRI by partial or total CNBr or acid cleavage of the protein. These fragments were isolated by preparative polyacrylamide gel electrophoresis in the presence of sodium dodecyl sulfate. They were analyzed in a qualitative manner for phosphodiesterase activity. Antibodies against these fragments were elicited in rats and tested for binding to native EcoRI in an enzyme-linked immunoassay. We conclude from these experiments that the DNA binding site of EcoRI is located in the COOH-terminal half of the molecule, close to and probably comprising amino acid residues 137 to 157. This conclusion is reinforced by the observation that this sequence shows homology to the sequences of the recognition helix of other gene-regulatory proteins.

摘要

我们通过对蛋白质进行部分或完全的溴化氰(CNBr)裂解或酸裂解,制备了多种限制性内切酶EcoRI的片段。这些片段在十二烷基硫酸钠存在的情况下,通过制备性聚丙烯酰胺凝胶电泳进行分离。对它们的磷酸二酯酶活性进行了定性分析。在大鼠体内引发了针对这些片段的抗体,并在酶联免疫测定中测试其与天然EcoRI的结合情况。我们从这些实验中得出结论,EcoRI的DNA结合位点位于分子的COOH末端一半,靠近并可能包含氨基酸残基137至157。这一序列与其他基因调节蛋白的识别螺旋序列具有同源性,这一观察结果进一步强化了这一结论。

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