Secondary structure of the 33 kDa, extrinsic protein of Photosystem II: a far-UV circular dichroism study
1994
Xu, Q. | Nelson, J. | Bricker, T.M.
The 33 kDa extrinsic protein of Photosystem II is an important component of the oxygen-evolving apparatus which functions to stabilize the manganese cluster at physiological chloride concentrations and to lower the calcium requirement for oxygen evolution. Chou-Fasman analysis of the amino-acid sequence of this protein suggests that this component contains a high proportion of alpha-helical structure and only relatively small amounts of beta-sheet structure. A computational study using more sophisticated techniques (Beauregard, M. (1992) Environ. Exp. Bot. 32, 411-429) concluded that the protein contained little periodically ordered secondary structure. In this we have directly measured the relative proportions of secondary structure present in the 33 kDa protein using far-ultraviolet circular dichroism spectroscopy. Our results indicate that, in solution, this protein contains a large proportion of beta-sheet structure (38%) and relatively small amounts of alpha-helical structure (9%). A structural model of the 33 kDa protein based on a constrained Chou-Fasman analysis (Teeter, M.M. and Whitlow, M (1988) Proteins 4, 262-273) is presented.
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