Literature DB >> 30560669

Ultra-Sensitive and Label-Free Probing of Binding Affinity Using Recognition Imaging.

Yoo Jin Oh1, Melanie Koehler1, Yoonhee Lee2, Sourav Mishra2, Joon Won Park2, Peter Hinterdorfer1.   

Abstract

Reliable quantification of binding affinity is important in biotechnology and pharmacology and increasingly coupled with a demand for ultrasensitivity, nanoscale resolution, and minute sample amounts. Standard techniques are not able to meet these criteria. This study provides a new platform based on atomic force microscopy (AFM)-derived recognition imaging to determine affinity by visualizing single molecular bindings on nanosize dendrons. Using DNA hybridization as a demonstrator, an AFM sensor adorned with a cognate binding strand senses and localizes target DNAs at nanometer resolution. To overcome the limitations of speed and resolution, the AFM cantilever is sinusoidally oscillated close to resonance conditions at small amplitudes. The equilibrium dissociation constant of capturing DNA duplexes was obtained, yielding 2.4 × 10-10 M. Our label-free single-molecular biochemical analysis approach evidences the utility of recognition imaging and analysis in quantifying biomolecular interactions of just a few hundred molecules.

Entities:  

Keywords:  Affinity; DNA hybridization; molecular recognition; scanning probe microscopy; single-molecule

Mesh:

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Year:  2018        PMID: 30560669     DOI: 10.1021/acs.nanolett.8b04883

Source DB:  PubMed          Journal:  Nano Lett        ISSN: 1530-6984            Impact factor:   12.262


  2 in total

1.  Direct imaging of antigen-antibody binding by atomic force microscopy.

Authors:  Jing Hu; Mingyan Gao; Zuobin Wang; Yujuan Chen; Zhengxun Song; Hongmei Xu
Journal:  Appl Nanosci       Date:  2020-09-24       Impact factor: 3.674

2.  Interdomain Linker Effect on the Mechanical Stability of Ig Domains in Titin.

Authors:  Bei Tong; Fang Tian; Peng Zheng
Journal:  Int J Mol Sci       Date:  2022-08-30       Impact factor: 6.208

  2 in total

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