5LSE

PHOTOSYNTHETIC REACTION CENTER MUTANT WITH Glu L212 replaced with Ala (CHAIN L, EL212W), Asp L213 replaced with ALA (Chain L, DL213A) AND LEU M215 REPLACED WITH ALA (CHAIN M, LM215A)

5LSE の概要

• エントリーDOI: 10.2210/pdb5lse/pdb
• 分子名称: Reaction center protein L chain, LAURYL DIMETHYLAMINE-N-OXIDE, PHOSPHATE ION, ... (13 entities in total)
• 機能のキーワード: transmembrane, electron transport, photosynthesis
• 由来する生物種: Rhodobacter sphaeroides; 詳細
• 細胞内の位置: Cellular chromatophore membrane; Multi-pass membrane protein: P0C0Y8 P0C0Y9; Cellular chromatophore membrane; Single-pass membrane protein: P0C0Y7
• タンパク質・核酸の鎖数: 3
• 化学式量合計: 104567.99

構造登録者

Fyfe, P.K.,Jones, M.R. (登録日: 2016-08-25, 公開日: 2016-11-09, 最終更新日: 2024-05-01)

主引用文献

Friebe, V.M.,Swainsbury, D.J.,Fyfe, P.K.,van der Heijden, W.,Jones, M.R.,Frese, R.N.
On the mechanism of ubiquinone mediated photocurrent generation by a reaction center based photocathode.
Biochim.Biophys.Acta, 1857:1925-1934, 2016

PubMed Abstract: Upon photoexcitation, the reaction center (RC) pigment-proteins that facilitate natural photosynthesis achieve a metastable separation of electrical charge among the embedded cofactors. Because of the high quantum efficiency of this process, there is a growing interest in their incorporation into biohybrid materials for solar energy conversion, bioelectronics and biosensing. Multiple bioelectrochemical studies have shown that reaction centers from various photosynthetic organisms can be interfaced with diverse electrode materials for the generation of photocurrents, but many mechanistic aspects of native protein functionality in a non-native environment is unknown. In vivo, RC's catalyse ubiquinone-10 reduction, protonation and exchange with other lipid phase ubiquinone-10s via protein-controlled spatial orientation and protein rearrangement. In contrast, the mechanism of ubiquinone-0 reduction, used to facilitate fast RC turnover in an aqueous photoelectrochemical cell (PEC), may not proceed via the same pathway as the native cofactor. In this report we show truncation of the native isoprene tail results in larger RC turnover rates in a PEC despite the removal of the tail's purported role of ubiquinone headgroup orientation and binding. Through the use of reaction centers with single or double mutations, we also show the extent to which two-electron/two-proton ubiquinone chemistry that operates in vivo also underpins the ubiquinone-0 reduction by surface-adsorbed RCs in a PEC. This reveals that only the ubiquinone headgroup is critical to the fast turnover of the RC in a PEC and provides insight into design principles for the development of new biophotovoltaic cells and biosensors.

PubMed: 27687473
DOI: 10.1016/j.bbabio.2016.09.011

実験手法

X-RAY DIFFRACTION (2.5 Å)