Single-molecule recognition of biomolecular interaction via Kelvin probe force microscopy.

Citation data:

ACS nano, ISSN: 1936-086X, Vol: 5, Issue: 9, Page: 6981-90

Publication Year:
2011
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Citations 19
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Repository URL:
http://scholarworks.unist.ac.kr/handle/201301/12301
PMID:
21806048
DOI:
10.1021/nn201540c
Author(s):
Park, Jinsung, Yang, Jaemoon, Lee, Gyudo, Lee, Chang Young, Na, Sungsoo, Lee, Sang Woo, Haam, Seungjoo, Huh, Yong-Min, Yoon, Dae Sung, Eom, Kilho, Kwon, Taeyun Show More Hide
Publisher(s):
American Chemical Society (ACS), AMER CHEMICAL SOC
Tags:
Materials Science, Engineering, Physics and Astronomy, single molecule, biomolecular interactions, protein kinase, Kelvin probe force microscopy, label-free, surface potential
article description
We report the scanning probe microscope (SPM)-based single-molecule recognition of biomolecular interactions between protein kinase and small ligands (i.e., ATP and Imatinib). In general, it is difficult to sense and detect the small ligands bound to protein kinase (at single-molecule resolution) using a conventional atomic force microscope (AFM) due to the limited resolution of conventional AFM for detecting the miniscule changes in molecular size driven by ligand binding. In this study, we have demonstrated that Kelvin probe force microscopy (KPFM) is able to articulate the surface potential of biomolecules interacting with ligands (i.e., the protein kinase-ATP interactions and inhibition phenomena induced by antagonistic molecules) in a label-free manner. Furthermore, measured surface potentials for biomolecular interactions enable quantitative descriptions on the ability of protein kinase to interact with small ligands such as ATP or antagonistic molecules. Our study sheds light on KPFM that allows the precise recognition of single-molecule interactions, which opens a new avenue for the design and development of novel molecular therapeutics.

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