Note to users. If you're seeing this message, it means that your browser cannot find this page's style/presentation instructions -- or possibly that you are using a browser that does not support current Web standards. Find out more about why this message is appearing, and what you can do to make your experience of our site the best it can be.
Invitrogen

Site Tools

  • AAAS
  • Subscribe
  • Feedback

Site Search

Search Advanced

Science 9 May 2008:
Vol. 320. no. 5877, pp. 794 - 797
DOI: 10.1126/science.1154800

Reports

Architecture of a Charge-Transfer State Regulating Light Harvesting in a Plant Antenna Protein

Tae Kyu Ahn,1,2* Thomas J. Avenson,2,3* Matteo Ballottari,4 Yuan-Chung Cheng,2 Krishna K. Niyogi,1,3 Roberto Bassi,4{dagger} Graham R. Fleming1,2{dagger}

Energy-dependent quenching of excess absorbed light energy (qE) is a vital mechanism for regulating photosynthetic light harvesting in higher plants. All of the physiological characteristics of qE have been positively correlated with charge transfer between coupled chlorophyll and zeaxanthin molecules in the light-harvesting antenna of photosystem II (PSII). We found evidence for charge-transfer quenching in all three of the individual minor antenna complexes of PSII (CP29, CP26, and CP24), and we conclude that charge-transfer quenching in CP29 involves a delocalized state of an excitonically coupled chlorophyll dimer. We propose that reversible conformational changes in CP29 can "tune" the electronic coupling between the chlorophylls in this dimer, thereby modulating the energy of the chlorophyll-zeaxanthin charge-transfer state and switching on and off the charge-transfer quenching during qE.

1 Physical Biosciences Division, Lawrence Berkeley National Laboratory, Berkeley, CA 94720, USA.
2 Department of Chemistry and QB3 Institute, University of California, Berkeley, CA 94720, USA.
3 Department of Plant and Microbial Biology, 111 Koshland Hall, University of California, Berkeley, CA 94720, USA.
4 Department of Science and Technology, University of Verona, 37134 Verona, Italy.

* These authors contributed equally to this work.

{dagger} To whom correspondence should be addressed. E-mail: grfleming{at}lbl.gov (G.R.F.); bassi{at}sci.univr.it (R.B.)

Read the Full Text





ADVERTISEMENT
Click Me!

ADVERTISEMENT
Click Me!

To Advertise     Find Products


Science. ISSN 0036-8075 (print), 1095-9203 (online)