Conformational constraints of cyclopentane peptide nucleic acids facilitate tunable binding to DNA

环戊烷肽核酸的构象限制有利于与 DNA 的可调结合

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作者:Hongchao Zheng, Istvan Botos, Victor Clausse, Herman Nikolayevskiy, Elizabeth E Rastede, Munira F Fouz, Sharlyn J Mazur, Daniel H Appella

Abstract

We report a series of synthetic, nucleic acid mimics with highly customizable thermodynamic binding to DNA. Incorporation of helix-promoting cyclopentanes into peptide nucleic acids (PNAs) increases the melting temperatures (Tm) of PNA+DNA duplexes by approximately +5°C per cyclopentane. Sequential addition of cyclopentanes allows the Tm of PNA + DNA duplexes to be systematically fine-tuned from +5 to +50°C compared with the unmodified PNA. Containing only nine nucleobases and an equal number of cyclopentanes, cpPNA-9 binds to complementary DNA with a Tm around 90°C. Additional experiments reveal that the cpPNA-9 sequence specifically binds to DNA duplexes containing its complementary sequence and functions as a PCR clamp. An X-ray crystal structure of the cpPNA-9-DNA duplex revealed that cyclopentanes likely induce a right-handed helix in the PNA with conformations that promote DNA binding.

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