Complex pathways in folding of protein G explored by simulation and experiment

Lisa J. Lapidus, Srabasti Acharya, Christian R. Schwantes, Ling Wu, Diwakar Shukla, Michael King, Stephen J. Decamp, Vijay S. Pande

Research output: Contribution to journalArticlepeer-review

Abstract

The B1 domain of protein G has been a classic model system of folding for decades, the subject of numerous experimental and computational studies. Most of the experimental work has focused on whether the protein folds via an intermediate, but the evidence is mostly limited to relatively slow kinetic observations with a few structural probes. In this work we observe folding on the submillisecond timescale with microfluidic mixers using a variety of probes including tryptophan fluorescence, circular dichroism, and photochemical oxidation. We find that each probe yields different kinetics and compare these observations with a Markov State Model constructed from large-scale molecular dynamics simulations and find a complex network of states that yield different kinetics for different observables. We conclude that there are many folding pathways before the final folding step and that these paths do not have large free energy barriers.

Original languageEnglish (US)
Pages (from-to)947-955
Number of pages9
JournalBiophysical journal
Volume107
Issue number4
DOIs
StatePublished - Aug 19 2014
Externally publishedYes

ASJC Scopus subject areas

  • Biophysics

Fingerprint Dive into the research topics of 'Complex pathways in folding of protein G explored by simulation and experiment'. Together they form a unique fingerprint.

Cite this