Direct observation of barrier-limited folding of BBL by single-molecule fluorescence resonance energy transfer.

ABSTRACT: One controversial area in protein folding mechanisms is whether some small, ultra-fast-folding proteins exist in distinct native and denatured state ensembles, separated by an energy barrier, or if there is a continuum of states between native and denatured. In theory, the simplest way of distinguishing between single-state barrierless or "downhill" folding and conventional separate state folding is by single-molecule spectroscopy, which can detect either distinct populations of proteins or a continuum. But, the time resolution of approximately 1 ms of most confocal fluorescence microscopes for single-molecule fluorescence resonance energy transfer (SM-FRET) is longer than that for the structural relaxation of proteins such as BBL, whose mechanism of folding is controversial. We have const

SUBMITTER: Huang F 

PROVIDER: S-EPMC2742407 | biostudies-literature | 2009 Sep

REPOSITORIES: biostudies-literature