Förster Energy Transfer Theory As Reflected in the Structures of Photosynthetic Light-harvesting Systems

Overview

Journal Chemphyschem

Specialty Chemistry

Date 2011 Feb 24

PMID 21344591

Citations 48

Authors

Melih Sener

Johan Strumpfer

Jen Hsin

Danielle Chandler

Simon Scheuring

C Neil Hunter

Klaus Schulten

Affiliations

Soon will be listed here.

Abstract

Förster’s theory of resonant energy transfer underlies a fundamental process in nature, namely the harvesting of sunlight by photosynthetic life forms. The theoretical framework developed by Förster and others describes how electronic excitation migrates in the photosynthetic apparatus of plants, algae, and bacteria from light absorbing pigments to reaction centers where light energy is utilized for the eventual conversion into chemical energy. The demand for highest possible efficiency of light harvesting appears to have shaped the evolution of photosynthetic species from bacteria to plants which, despite a great variation in architecture, display common structural themes founded on the quantum physics of energy transfer as described first by Förster. Herein, Förster’s theory of excitation transfer is summarized, including recent extensions, and the relevance of the theory to photosynthetic systems as evolved in purple bacteria, cyanobacteria, and plants is demonstrated. Förster’s energy transfer formula, as used widely today in many fields of science, is also derived.

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References

Koepke J, Hu X, Muenke C, Schulten K, Michel H . The crystal structure of the light-harvesting complex II (B800-850) from Rhodospirillum molischianum. Structure. 1996; 4(5):581-97. DOI: 10.1016/s0969-2126(96)00063-9. View

Emerson R, Arnold W . THE PHOTOCHEMICAL REACTION IN PHOTOSYNTHESIS. J Gen Physiol. 2009; 16(2):191-205. PMC: 2141200. DOI: 10.1085/jgp.16.2.191. View

Ishizaki A, Fleming G . On the adequacy of the Redfield equation and related approaches to the study of quantum dynamics in electronic energy transfer. J Chem Phys. 2009; 130(23):234110. DOI: 10.1063/1.3155214. View

Hsin J, Chandler D, Gumbart J, Harrison C, Sener M, Strumpfer J . Self-assembly of photosynthetic membranes. Chemphyschem. 2010; 11(6):1154-9. PMC: 3086839. DOI: 10.1002/cphc.200900911. View

Strumpfer J, Schulten K . Light harvesting complex II B850 excitation dynamics. J Chem Phys. 2009; 131(22):225101. PMC: 2802260. DOI: 10.1063/1.3271348. View

Sener M, Park S, Lu D, Damjanovic A, Ritz T, Fromme P . Excitation migration in trimeric cyanobacterial photosystem I. J Chem Phys. 2004; 120(23):11183-95. DOI: 10.1063/1.1739400. View

Chen L, Zheng R, Shi Q, Yan Y . Optical line shapes of molecular aggregates: hierarchical equations of motion method. J Chem Phys. 2009; 131(9):094502. DOI: 10.1063/1.3213013. View

Gobets B, van Stokkum I, Rogner M, Kruip J, Schlodder E, Karapetyan N . Time-resolved fluorescence emission measurements of photosystem I particles of various cyanobacteria: a unified compartmental model. Biophys J. 2001; 81(1):407-24. PMC: 1301521. DOI: 10.1016/S0006-3495(01)75709-8. View

Scheuring S, Sturgis J, Prima V, Bernadac A, Levy D, Rigaud J . Watching the photosynthetic apparatus in native membranes. Proc Natl Acad Sci U S A. 2004; 101(31):11293-7. PMC: 509197. DOI: 10.1073/pnas.0404350101. View

10.

Tucker J, Siebert C, Escalante M, Adams P, Olsen J, Otto C . Membrane invagination in Rhodobacter sphaeroides is initiated at curved regions of the cytoplasmic membrane, then forms both budded and fully detached spherical vesicles. Mol Microbiol. 2010; 76(4):833-47. DOI: 10.1111/j.1365-2958.2010.07153.x. View

11.

Hu X, Damjanovic A, Ritz T, Schulten K . Architecture and mechanism of the light-harvesting apparatus of purple bacteria. Proc Natl Acad Sci U S A. 1998; 95(11):5935-41. PMC: 34498. DOI: 10.1073/pnas.95.11.5935. View

12.

Damjanovic A, Kosztin I, Kleinekathofer U, Schulten K . Excitons in a photosynthetic light-harvesting system: a combined molecular dynamics, quantum chemistry, and polaron model study. Phys Rev E Stat Nonlin Soft Matter Phys. 2002; 65(3 Pt 1):031919. DOI: 10.1103/PhysRevE.65.031919. View

13.

Scheuring S, Sturgis J . Atomic force microscopy of the bacterial photosynthetic apparatus: plain pictures of an elaborate machinery. Photosynth Res. 2009; 102(2-3):197-211. DOI: 10.1007/s11120-009-9413-7. View

14.

Amunts A, Toporik H, Borovikova A, Nelson N . Structure determination and improved model of plant photosystem I. J Biol Chem. 2009; 285(5):3478-86. PMC: 2823434. DOI: 10.1074/jbc.M109.072645. View

15.

Camara-Artigas A, Brune D, Allen J . Interactions between lipids and bacterial reaction centers determined by protein crystallography. Proc Natl Acad Sci U S A. 2002; 99(17):11055-60. PMC: 123209. DOI: 10.1073/pnas.162368399. View

16.

Siebert C, Qian P, Fotiadis D, Engel A, Hunter C, Bullough P . Molecular architecture of photosynthetic membranes in Rhodobacter sphaeroides: the role of PufX. EMBO J. 2004; 23(4):690-700. PMC: 381000. DOI: 10.1038/sj.emboj.7600092. View

17.

Guskov A, Kern J, Gabdulkhakov A, Broser M, Zouni A, Saenger W . Cyanobacterial photosystem II at 2.9-A resolution and the role of quinones, lipids, channels and chloride. Nat Struct Mol Biol. 2009; 16(3):334-42. DOI: 10.1038/nsmb.1559. View

18.

Rutkauskas D, Novoderezhkin V, Cogdell R, van Grondelle R . Fluorescence spectroscopy of conformational changes of single LH2 complexes. Biophys J. 2004; 88(1):422-35. PMC: 1305019. DOI: 10.1529/biophysj.104.048629. View

19.

Jungas C, Ranck J, RIGAUD J, Joliot P, Vermeglio A . Supramolecular organization of the photosynthetic apparatus of Rhodobacter sphaeroides. EMBO J. 1999; 18(3):534-42. PMC: 1171146. DOI: 10.1093/emboj/18.3.534. View

20.

Cogdell R, Gall A, Kohler J . The architecture and function of the light-harvesting apparatus of purple bacteria: from single molecules to in vivo membranes. Q Rev Biophys. 2006; 39(3):227-324. DOI: 10.1017/S0033583506004434. View