4.8 Article

Novel RNA base pair with higher specificity using single selenium atom

期刊

NUCLEIC ACIDS RESEARCH
卷 40, 期 11, 页码 5171-5179

出版社

OXFORD UNIV PRESS
DOI: 10.1093/nar/gks010

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资金

  1. USA National Foundation (NSF) [CHE-0750235, MCB-0824837]
  2. USA National Institute of Health (NIH) [GM095086]
  3. Georgia Cancer Coalition Distinguished Cancer Clinicians and Scientists award
  4. National Science Foundation [CHE-0750235]
  5. Direct For Biological Sciences
  6. Div Of Molecular and Cellular Bioscience [0824837] Funding Source: National Science Foundation

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Specificity of nucleobase pairing provides essential foundation for genetic information storage, replication, transcription and translation in all living organisms. However, the wobble base pairs, where U in RNA (or T in DNA) pairs with G instead of A, might compromise the high specificity of the base pairing. The U/G wobble pairing is ubiquitous in RNA, especially in non-coding RNA. In order to increase U/A pairing specificity, we have hypothesized to discriminate against U/G wobble pair by tailoring the steric and electronic effects at the 2-exo position of uridine and replacing the 2-exo oxygen with a selenium atom. We report here the first synthesis of the 2-Se-U-RNAs as well as the 2-Se-uridine (U-Se) phosphoramidite. Our biophysical and structural studies of the U-Se-RNAs indicate that this single atom replacement can indeed create a novel U/A base pair with higher specificity than the natural one. We reveal that the U-Se/A pair maintains a structure virtually identical to the native U/A base pair, while discriminating against U/G wobble pair. This oxygen replacement with selenium offers a unique chemical strategy to enhance the base pairing specificity at the atomic level.

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