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


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.

SUBMITTER: Su X 

PROVIDER: S-EPMC4677574 | biostudies-literature | 2015 Sep

REPOSITORIES: biostudies-literature

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

Su Xiaoye X   Zhou Xiao X   Zhang Nan N   Zhu Mengyuan M   Zhang Hong H   Jayawickramarajah Janarthanan J  

Chemical communications (Cambridge, England) 20150901 71


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 syste  ...[more]

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