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Updated: Sep 14, 2026

Proton Transfer and Protein Conformation Dynamics in Photosensitive Proteins by Time-resolved Step-scan Fourier-transform Infrared Spectroscopy
Published on: June 27, 2014
Influence of excitation energy on the bacteriorhodopsin photocycle
R W Hendler1, Z Dancsházy, S Bose
1Laboratory of Cell Biology, National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, Maryland 20892.
Abstract:
Kinetic curves for the bacteriorhodopsin (BR) photocycle were obtained both at 570 and at 412 nm at a series of increasing levels of intensity of the exciting laser. Singular value decomposition (SVD) of these curves showed two transitions in the kinetic profiles that occurred at specific levels of actinic light. This means that the photocycle was influenced by photon density in two ways. In a separate application of SVD, time-resolved optical spectra were analyzed at each of many levels of exciting laser intensities. The studies showed that the transition at the low level of laser intensity was due principally to an increase in the amount of BR that was turning over. The transition at the higher level of laser intensity showed a fundamental change in kinetics of the photocycle. At low intensity levels, the fast form of M (Mf) predominated, whereas at high levels the slow form of M (Ms) predominated. A distinction was found between Mf and Ms, in that the former decayed directly to the O intermediate whereas the latter decayed directly to BR.
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