Literature DB >> 22920279

A synthetic chemomechanical machine driven by ligand-receptor bonding.

Gabriel J Lavella1, Amol D Jadhav, Michel M Maharbiz.   

Abstract

The ability to create synthetic chemomechanical machines with engineered functionality promises large technological rewards. However, current efforts in molecular chemistry are restrained by the formidable challenges faced in molecular structure and function prediction. An alternative approach to engineering machines with tailorable chemomechanical functionality is to design Brownian ratchet devices using molecular assemblies. We demonstrate this through the creation of autonomous molecular machines that sense, mechanically react, and extract energy from ligand-receptor binding. We present a specific instantiation, measuring approximately 100 nm in length, which actuates upon detection of a streptavidin ligand. Machines were designed through the tailoring of energy landscapes on 3D DNA origami motifs. We also analyzed the response over a logarithmic concentration ratio (device:ligand) range from 1:10(1) to 1:10(5).

Mesh:

Substances:

Year:  2012        PMID: 22920279     DOI: 10.1021/nl3026136

Source DB:  PubMed          Journal:  Nano Lett        ISSN: 1530-6984            Impact factor:   11.189


  2 in total

1.  Programmable motion of DNA origami mechanisms.

Authors:  Alexander E Marras; Lifeng Zhou; Hai-Jun Su; Carlos E Castro
Journal:  Proc Natl Acad Sci U S A       Date:  2015-01-05       Impact factor: 11.205

2.  Regulation at a distance of biomolecular interactions using a DNA origami nanoactuator.

Authors:  Yonggang Ke; Travis Meyer; William M Shih; Gaetan Bellot
Journal:  Nat Commun       Date:  2016-03-18       Impact factor: 14.919

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.