| Literature DB >> 15595857 |
David E Hertzog1, Xavier Michalet, Marcus Jäger, Xiangxu Kong, Juan G Santiago, Shimon Weiss, Olgica Bakajin.
Abstract
We have developed a microfluidic mixer for studying protein folding and other reactions with a mixing time of 8 mus and sample consumption of femtomoles. This device enables us to access conformational changes under conditions far from equilibrium and at previously inaccessible time scales. In this paper, we discuss the design and optimization of the mixer using modeling of convective diffusion phenomena and a characterization of the mixer performance using microparticle image velocimetry, dye quenching, and Forster resonance energy-transfer (FRET) measurements of single-stranded DNA. We also demonstrate the feasibility of measuring fast protein folding kinetics using FRET with acyl-CoA binding protein.Mesh:
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Year: 2004 PMID: 15595857 PMCID: PMC1413504 DOI: 10.1021/ac048661s
Source DB: PubMed Journal: Anal Chem ISSN: 0003-2700 Impact factor: 6.986