TY - JOUR
T1 - Dynamic control of protein diffusion within the granal thylakoid lumen
AU - Kirchhoff, Helmut
AU - Hall, Chris
AU - Wood, Magnus
AU - Herbstova, Miroslava
AU - Tsabari, Onie
AU - Nevo, Reinat
AU - Charuvi, Dana
AU - Shimoni, Eyal
AU - Reich, Ziv
N1 - Washington State University; Binational Agricultural Research and Development Fund; Israel Science Foundation [1005/07]; Carolito Stiftung; Minerva FoundationWe thank Egbert Boekema and Roman Kouril for kindly providing the tomographic data used for modeling the photosystem II distributions. The photosystem II images shown in Figs. 2 and 3 (derived from ref. 15) were provided by Bertram Daum. The electron microscopy studies were conducted at the Irving and Cherna Moskowitz Center for Nano and Bio-Nano Imaging at the Weizmann Institute of Science. This study was supported in part by Washington State University (to H. K.); the Binational Agricultural Research and Development Fund (H. K. and Z.R.); and the Israel Science Foundation (1005/07), the Carolito Stiftung, and the Minerva Foundation (to Z.R.).
PY - 2011/12/13
Y1 - 2011/12/13
N2 - The machinery that conducts the light-driven reactions of oxygenic photosynthesis is hosted within specialized paired membranes called thylakoids. In higher plants, the thylakoids are segregated into two morphological and functional domains called grana and stroma lamellae. A large fraction of the luminal volume of the granal thylakoids is occupied by the oxygen-evolving complex of photosystem II. Electron microscopy data we obtained on dark- and light-adapted Arabidopsis thylakoids indicate that the granal thylakoid lumen significantly expands in the light. Models generated for the organization of the oxygen-evolving complex within the granal lumen predict that the light-induced expansion greatly alleviates restrictions imposed on protein diffusion in this compartment in the dark. Experiments monitoring the redox kinetics of the luminal electron carrier plastocyanin support this prediction. The impact of the increase in protein mobility within the granal luminal compartment in the light on photosynthetic electron transport rates and processes associated with the repair of photodamaged photosystem II complexes is discussed.
AB - The machinery that conducts the light-driven reactions of oxygenic photosynthesis is hosted within specialized paired membranes called thylakoids. In higher plants, the thylakoids are segregated into two morphological and functional domains called grana and stroma lamellae. A large fraction of the luminal volume of the granal thylakoids is occupied by the oxygen-evolving complex of photosystem II. Electron microscopy data we obtained on dark- and light-adapted Arabidopsis thylakoids indicate that the granal thylakoid lumen significantly expands in the light. Models generated for the organization of the oxygen-evolving complex within the granal lumen predict that the light-induced expansion greatly alleviates restrictions imposed on protein diffusion in this compartment in the dark. Experiments monitoring the redox kinetics of the luminal electron carrier plastocyanin support this prediction. The impact of the increase in protein mobility within the granal luminal compartment in the light on photosynthetic electron transport rates and processes associated with the repair of photodamaged photosystem II complexes is discussed.
UR - http://www.scopus.com/inward/record.url?scp=84055200485&partnerID=8YFLogxK
U2 - 10.1073/pnas.1104141109
DO - 10.1073/pnas.1104141109
M3 - مقالة
C2 - 22128333
SN - 0027-8424
VL - 108
SP - 20248
EP - 20253
JO - Proceedings of the National Academy of Sciences of the United States of America
JF - Proceedings of the National Academy of Sciences of the United States of America
IS - 50
ER -