Literature DB >> 26225890

A stable bidentate protein binder achieved via DNA self-assembly driven ligand migration.

Xiaoye Su1, Xiao Zhou, Nan Zhang, Mengyuan Zhu, Hong Zhang, Janarthanan Jayawickramarajah.   

Abstract

Herein we disclose the development of two complementary single stranded DNA-small molecule chimeras (DCs) that by themselves only bind weakly to a protein target (human serum albumin; HSA). However, upon self-assembly, the DC duplex facilitates a ligand migration reaction leading to a covalently fastened high-affinity, bidentate, protein-binder that resides at the terminus of only one of the DC strands. Due to this specific localization, the bidentate projection remains intact—and thus the system continues to strongly bind HSA—even under conditions that denature and degrade the DNA scaffolds.

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Year:  2015        PMID: 26225890      PMCID: PMC4677574          DOI: 10.1039/c5cc03213j

Source DB:  PubMed          Journal:  Chem Commun (Camb)        ISSN: 1359-7345            Impact factor:   6.222


  28 in total

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Journal:  Angew Chem Int Ed Engl       Date:  2008       Impact factor: 15.336

8.  DNA-encoded chemical libraries: advancing beyond conventional small-molecule libraries.

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9.  Efficient nucleic acid detection by templated reductive quencher release.

Authors:  Raphael M Franzini; Eric T Kool
Journal:  J Am Chem Soc       Date:  2009-11-11       Impact factor: 15.419

10.  Selective protein-surface sensing using ruthenium(II) tris(bipyridine) complexes.

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  1 in total

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