Improved selectivity for the binding of naphthyridine dimer to guanine-guanine mismatch

被引:105
作者
Nakatani, K [1 ]
Sando, S [1 ]
Saito, I [1 ]
机构
[1] Kyoto Univ, Fac Engn, Dept Synthet Chem & Biol Chem, CREST, Kyoto 6068501, Japan
关键词
D O I
10.1016/S0968-0896(01)00160-2
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Naphthyridine dimer composed of two 2-amino-1,8-naphthyridines and a connecting linker strongly binds to guanine-guanine (G-G) mismatch in duplex DNA. In order to improve G-G selectivity for the binding, we have examined structure modification of the linker. A new naphthyridine dimer possessing 3,6-diazaoctanedioic acid linker binds to G-G mismatch with an association constant of 1.18 x 10(7) M-1, which is somewhat weaker than that of the original naphthyridine dimer having a shorter connecting linker. However, the binding of the modified naphthyridine dimer to G-A mismatch was almost negligible as compared to that of the original. This results in a net increase of the selectivity for the binding to G-G mismatch by 4-folds. (C) 2001 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:2381 / 2385
页数:5
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