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Originally published as Biophys J. BioFAST on May 18, 2007.
doi:10.1529/biophysj.107.104554
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Biophysical Journal 93:2240-2254 (2007)
© 2007 The Biophysical Society

Chlorophyll Ring Deformation Modulates Qy Electronic Energy in Chlorophyll-Protein Complexes and Generates Spectral Forms

Giuseppe Zucchelli, Doriano Brogioli, Anna Paola Casazza, Flavio M. Garlaschi and Robert C. Jennings

Consiglio Nazionale Delle Ricerche-Istituto di Biofisica, Dipartimento di Biologia, Università degli Studi di Milano, Milan, Italy

Correspondence: Address reprint requests to G. Zucchelli, E-mail: giuseppe.zucchelli{at}unimi.it.

The possibility that the chlorophyll (chl) ring distortions observed in the crystal structures of chl-protein complexes are involved in the transition energy modulation, giving rise to the spectral forms, is investigated. The out-of-plane chl-macrocycle distortions are described using an orthonormal set of deformations, defined by the displacements along the six lowest-frequency, out-of-plane normal coordinates. The total chl-ring deformation is the linear combination of these six deformations. The two higher occupied and the two lower unoccupied chl molecular orbitals, which define the Qy electronic transition, have the same symmetry as four of the six out-of-plane lowest frequency modes. We assume that a deformation along the normal-coordinate having the same symmetry as a given molecular orbital will perturb that orbital and modify its energy. The changes in the chl Qy transition energies are evaluated in the Peridinin-Chl-Protein complex and in light harvesting complex II (LHCII), using crystallographic data. The macrocycle deformations induce a distribution of the chl Qy electronic energy transitions which, for LHCII, is broader for chla than for chlb. This provides the physical mechanism to explain the long-held view that the chla spectral forms in LHCII are both more numerous and cover a wider energy range than those of chlb.







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Copyright © 2007 by the Biophysical Society.