期刊
ANALYTICAL CHEMISTRY
卷 76, 期 24, 页码 7169-7178出版社
AMER CHEMICAL SOC
DOI: 10.1021/ac048661s
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资金
- NHLBI NIH HHS [N01HV28183, N01-HV-28183] Funding Source: Medline
- NIGMS NIH HHS [1R01-GM65382, R01 GM065382] Funding Source: Medline
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.
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