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改变阻遏物的DNA结合特异性。

Changing the DNA-binding specificity of a repressor.

作者信息

Youderian P, Vershon A, Bouvier S, Sauer R T, Susskind M M

出版信息

Cell. 1983 Dec;35(3 Pt 2):777-83. doi: 10.1016/0092-8674(83)90110-1.

Abstract

The Mnt repressor of Salmonella phage P22 recognizes a 17 base pair operator. We constructed an Mnt binding site with two symmetric operator-constitutive mutations. We then selected Mnt mutants that have lost the ability to bind the wild-type operator but acquired the ability to bind the mutant operator. Four independent mutations change the same CAC codon in the mnt gene to CCT or CCC. The corresponding amino acid change in Mnt is His6 leads to Pro. DNA binding assays with purified wild-type and mutant proteins confirm the change of binding specificity in vitro. Wild-type Mnt binds strongly to the wild-type operator, but binds the mutant operator with 1000-fold less affinity. The mutant Mnt binds with converse affinities to the two operators.

摘要

沙门氏菌噬菌体P22的Mnt阻遏蛋白识别一个17个碱基对的操纵基因。我们构建了一个带有两个对称的操纵基因组成型突变的Mnt结合位点。然后我们筛选出了失去结合野生型操纵基因能力但获得结合突变型操纵基因能力的Mnt突变体。四个独立的突变将mnt基因中相同的CAC密码子变为CCT或CCC。Mnt中相应的氨基酸变化是His6变为Pro。用纯化的野生型和突变型蛋白进行的DNA结合试验证实了体外结合特异性的改变。野生型Mnt与野生型操纵基因强烈结合,但与突变型操纵基因的结合亲和力低1000倍。突变型Mnt与这两个操纵基因的结合亲和力则相反。

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