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Uncovering the interactions driving carotenoid binding in light-harvesting complexes

Authors :
Vincenzo Mascoli
Roberta Croce
Lorenzo Cupellini
Nicoletta Liguori
Eduard Elias
Benedetta Mennucci
Biophysics Photosynthesis/Energy
LaserLaB - Energy
Source :
Chemical Science, Mascoli, V, Liguori, N, Cupellini, L, Elias, E, Mennucci, B & Croce, R 2021, ' Uncovering the interactions driving carotenoid binding in light-harvesting complexes ', Chemical Science, vol. 12, no. 14, pp. 5113-5122 . https://doi.org/10.1039/d1sc00071c, Chemical Science, 12(14), 5113-5122. Royal Society of Chemistry
Publication Year :
2021
Publisher :
Royal Society of Chemistry (RSC), 2021.

Abstract

Carotenoids are essential constituents of plant light-harvesting complexes (LHCs), being involved in protein stability, light harvesting, and photoprotection. Unlike chlorophylls, whose binding to LHCs is known to require coordination of the central magnesium, carotenoid binding relies on weaker intermolecular interactions (such as hydrogen bonds and van der Waals forces), whose character is far more elusive. Here we addressed the key interactions responsible for carotenoid binding to LHCs by combining molecular dynamics simulations and polarizable quantum mechanics/molecular mechanics calculations on the major LHC, LHCII. We found that carotenoid binding is mainly stabilized by van der Waals interactions with the surrounding chlorophyll macrocycles rather than by hydrogen bonds to the protein, the latter being more labile than predicted from structural data. Furthermore, the interaction network in the binding pockets is relatively insensitive to the chemical structure of the embedded carotenoid. Our results are consistent with a number of experimental data and challenge the role played by specific interactions in the assembly of pigment-protein complexes.<br />Carotenoids are essential constituents of plant light-harvesting complexes. This in silico study shows that carotenoid binding is mainly driven by van der Waals interactions with the surrounding chlorophylls rather than hydrogen bonds to the protein.

Details

ISSN :
20416539 and 20416520
Volume :
12
Database :
OpenAIRE
Journal :
Chemical Science
Accession number :
edsair.doi.dedup.....805f787b2c78c9a587e0e44b6032c1aa