2011 OSU Molecular Life Sciences
Interdisciplinary Graduate Programs Symposium
Poster abstracts
Abstract:
Hydration dynamics in the immediate vicinity of a protein, probed by time-dependent fluorescence Stokes shift experiments, is critical to understand its biological function. Protein Stokes shifts typically exhibit biphasic
relaxation following photo-excitation: fast relaxation occurs on a time scale of
several picoseconds while slower components indicate additional hydration dynamics on a time scale of tens of picoseconds, or longer. Theoretical
studies using both linear response and non-equilibrium molecular dynamics (MD)
calculation qualitatively reproduce the observed biphasic behavior of time dependent Stokes shift for Trp-7 (W7) in myoglobin.
Comparison with constrained MD simulations with protein frozen at the instant of
photo-excitation reveals the molecular mechanism of slow hydration process and establishes the critical role of protein flexibility. Coupled
protein-water motion is shown to be necessary for the observation of the slow
component of hydration dynamics. Qualitatively similar results are found for a series of additional cases, such as monellin and staph. nuclease. We
illustrate why tracking the separate contributions to the Stokes shift without
constrained MD studies may not yield an accurate interpretation of protein hydration dynamics. Additionally, we examine the extent to which protein
fluctuations obey Gaussian statistics and the linear response approximation to the Stokes shift is valid. Equilibrium fluctuations of the ground-excited energy difference, which control the absorption and fluorescence
line shapes, in the ground and excited electronic states are not independent of
each other. We illustrate how small differences from Gaussian statistics in one electronic state can be a signature of very significant deviations
from linear response theory, such as isomerization, in the other electronic state.
Keywords: Hydration dynamics, fluorescence Stokes shift, slow component