Walker W L, Kopka M L, Goodsell D S
Department of Biomathematics, University of California at Los Angeles 90095, USA.
Biopolymers. 1997;44(4):323-34. doi: 10.1002/(SICI)1097-0282(1997)44:4<323::AID-BIP2>3.0.CO;2-0.
Sequence-specific polyamides that bind in the minor groove of DNA are attractive candidates for antibiotics, cancer chemotherapeutics, and transcriptional antagonists. This paper reviews the progress of structure-based design of minor-groove-binding polyamides, from the first structure of netropsin with DNA, to the effective linked polyamides currently under study. A theory of polyamide specificity is also reviewed, introducing methods to determine the optimal strategies for targeting a given DNA sequence within a genome of competing sequences.
在DNA小沟中结合的序列特异性聚酰胺,是抗生素、癌症化疗药物和转录拮抗剂的理想候选物。本文综述了基于结构设计小沟结合聚酰胺的进展,从放线菌素与DNA的首个结构,到目前正在研究的有效连接聚酰胺。还综述了聚酰胺特异性理论,介绍了在竞争序列基因组中确定靶向给定DNA序列的最佳策略的方法。