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2:1吡咯-咪唑聚酰胺-DNA基序的结合位点大小限制

Binding site size limit of the 2:1 pyrrole-imidazole polyamide-DNA motif.

作者信息

Kelly J J, Baird E E, Dervan P B

机构信息

Division of Chemistry and Chemical Engineering, California Institute of Technology, Pasadena, CA 91125, USA.

出版信息

Proc Natl Acad Sci U S A. 1996 Jul 9;93(14):6981-5. doi: 10.1073/pnas.93.14.6981.

Abstract

Polyamides containing N-methylimidazole (Im) and N-methylpyrrole (Py) amino acids can be combined in antiparallel side-by-side dimeric complexes for sequence-specific recognition in the minor groove of DNA. Six polyamides containing three to eight rings bind DNA sites 5-10 bp in length, respectively. Quantitative DNase I footprint titration experiments demonstrate that affinity maximizes and is similar at ring sizes of five, six, and seven. Sequence specificity decreases as the length of the polyamides increases beyond five rings. These results provide useful guidelines for the design of new polyamides that bind longer DNA sites with enhanced affinity and specificity.

摘要

含有N-甲基咪唑(Im)和N-甲基吡咯(Py)氨基酸的聚酰胺可以组合成反平行并排的二聚体复合物,用于在DNA小沟中进行序列特异性识别。六种含有三到八个环的聚酰胺分别与长度为5 - 10个碱基对的DNA位点结合。定量DNase I足迹滴定实验表明,在环大小为五、六和七时亲和力最大且相似。当聚酰胺的长度超过五个环时,序列特异性降低。这些结果为设计能以增强的亲和力和特异性结合更长DNA位点的新型聚酰胺提供了有用的指导方针。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ad7f/38920/3b0d67a2e187/pnas01518-0147-a.jpg

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