Abstract
Testing
the premise of evolutionarily optimized protein dynamics has remained an experimental
challenge. Most measurements fail to
isolate specific structural motions. Our
simulations show that the structural variation of a single protein in time
results in variation in the vibrations leading to the observed broad and
featureless optical absorption. However,
when the thermal population of a protein’s configurations are considered,
vibrations with functional displacements are concentrated in specific frequency
bands. These emergent dynamics are
apparent in anisotropic optical absorbance, indicating an experimental avenue
for measuring these motions and their impact on biological function.
Supplementary materials
Title
Romo NMEA SI
Description
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