Role of Arg-72 of pharaonis Phoborhodopsin (sensory rhodopsin II) on its photochemistry |
| |
Authors: | Ikeura Yukako Shimono Kazumi Iwamoto Masayuki Sudo Yuki Kamo Naoki |
| |
Affiliation: | Laboratory of Biophysical Chemistry, Graduate School of Pharmaceutical Sciences, Hokkaido University, Sapporo, Japan. |
| |
Abstract: | Pharaonis phoborhodopsin (ppR, or pharaonis sensory rhodopsin II, NpsRII) is a sensor for the negative phototaxis of Natronomonas (Natronobacterium) pharaonis. Arginine 72 of ppR corresponds to Arg-82 of bacteriorhodopsin, which is a highly conserved residue among microbial rhodopsins. Using various Arg-72 ppR mutants, we obtained the following results: 1). Arg-72(ppR) together possibly with Asp-193 influenced the pK(a) of the counterion of the protonated Schiff base. 2). The M-rise became approximately four times faster than the wild-type. 3). Illumination causes proton uptake and release, and the pH profiles of the sequence of these two proton movements were different between R72A mutant and the wild-type; it is inferred that Arg-72 connects the proton transfer events occurring at both the Schiff base and an extracellular proton-releasing residue (Asp-193). 4). The M-decays of Arg-72 mutants were faster ( approximately 8-27 folds at pH 8 depending on mutants) than the wild-type, implying that the guanidinium prevents the proton transfer from the extracellular space to the deprotonated Schiff base. 5), The proton-pumping activities were decreased for mutants having increased M-decay rates, but the extent of the decrease was smaller than expected. The role of Arg-72 of ppR on the photochemistry was discussed. |
| |
Keywords: | bR, bacteriorhodopsin hR, halorhodopsin sR, sensory rhodopsin pR, phoborhodopsin ppR, pharaonis phoborhodopsin (sensory rhodopsin II) NpsRII, pharaonis sensory rhodopsin II pHtrII, halobacterial transducer for pharaonis phoborhodopsin (sensory rhodopsin II) Arg-82bR, arginine residue at 82nd position of bR Arg-72ppR, arginine residue at 72nd position of ppR EC, extracellular channel CP, cytoplasmic channel R72AppR, mutant in which Arg-72ppR is replaced with Ala |
本文献已被 ScienceDirect PubMed 等数据库收录! |
|