Light Harvesting by Equally Contributing Mechanisms in a Photosynthetic Antenna Protein
Source abstract
Abstract
We report supramolecular quantum mechanics/molecular mechanics simulations on the peridinin–chlorophyll a protein (PCP) complex from the causative algal species of red tides. These calculations reproduce for the first time quantitatively the distinct peridinin absorptions, identify multichromophoric molecular excitations, and elucidate the mechanisms regulating the strongly allowed S 0 (1 1 A g – ) → S 2 (1 1 B u + ) absorptions of the bound peridinins that span a 58 nm spectral range in the region of maximal solar irradiance. We discovered that protein binding site-imposed conformations, local electrostatics, and electronic coupling contribute equally to the spectral inhomogeneity. Electronic coupling causes coherent excitations among the densely packed pigments. Complementary pairing of tuning mechanisms is the result of a competition between pigment–pigment and pigment–environment interactions. We found that the aqueous solvent works in concert with the charge distribution of PCP to produce a strong correlation between peridinin spectral bathochromism and the local dielectric environment.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Photosynthetic Processes and Mechanisms · Photoreceptor and optogenetics research · Light effects on plants
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Chemistry, University of Connecticut, Storrs, Connecticut 06269-3060, United States
Funding
Division of Chemistry · Division of Graduate Education
References (24)
Show source-provided references
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