4.4 Article

Synthesis of DNA-Binding Peptoids

期刊

SYNLETT
卷 26, 期 11, 页码 1581-1585

出版社

GEORG THIEME VERLAG KG
DOI: 10.1055/s-0034-1380698

关键词

triazine; cyanuric chloride; peptide synthesis; assembly; PNA; peptoids

资金

  1. NSF
  2. Division Of Materials Research
  3. Direct For Mathematical & Physical Scien [1410232] Funding Source: National Science Foundation

向作者/读者索取更多资源

Programmable molecular recognition through nucleic acid base pairing has enabled applications in nano- and biotechnology using DNA, RNA, PNA, and more recently, bifacial PNA (bPNA). We describe herein the synthesis and DNA recognition properties of peptoid backbones bearing the bifacial synthetic nucleobase melamine. These peptoid nucleic acids' hybridize with thymine-rich DNA, like their peptide cognate (bPNA). DNA complexation is highly sensitive to peptoid side-chain length and overall charge. Peptoids isomeric with peptide bPNA were less efficient at DNA recognition, possibly due to conformational and steric differences. 1 Triazines and DNA Molecular Recognition 2 Synthesis of DNA-Binding Peptoids 3 Peptoid-DNA Binding Studies

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