Occupancy and functional architecture of the pigment binding sites of photosystem II antenna complex Lhcb5.

ABSTRACT: Lhcb5 is an antenna protein that is highly conserved in plants and green algae. It is part of the inner layer of photosystem II antenna system retained in high light acclimated plants. To study the structure-function relation and the role of individual pigments in this complex, we (i) "knocked out" each of the chromophores bound to multiple (nine total) chlorophyll sites and (ii) exchanged the xanthophylls bound to the three xanthophyll sites. The occupancy and associated energy of the pigment binding sites were determined. The role of the individual pigments in protein folding, stability, energy transfer, and dissipation was studied in vitro. The results indicate that lutein has a primary role in the folding and stability of the complex, whereas violaxanthin and zeaxanthin have a negative

SUBMITTER: Ballottari M 

PROVIDER: S-EPMC2658104 | biostudies-literature | 2009 Mar

REPOSITORIES: biostudies-literature