Literature DB >> 23062114

Influence of halide binding on the hydrogen bonding network in the active site of Salinibacter sensory rhodopsin I.

Louisa Reissig1, Tatsuya Iwata, Takashi Kikukawa, Makoto Demura, Naoki Kamo, Hideki Kandori, Yuki Sudo.   

Abstract

In nature, organisms are subjected to a variety of environmental stimuli to which they respond and adapt. They can show avoidance or attractive behaviors away from or toward such stimuli in order to survive in the various environments in which they live. One such stimuli is light, to which, for example, the receptor sensory rhodopsin I (SRI) has been found to respond by regulating both negative and positive phototaxis in, e.g., the archaeon Halobacterium salinarum. Interestingly, to date, all organisms having SRI-like proteins live in highly halophilic environments, suggesting that salt significantly influences the properties of SRIs. Taking advantage of the discovery of the highly stable SRI homologue from Salinibacter ruber (SrSRI), which maintains its color even in the absence of salt, the importance of the chloride ion for the color tuning and for the slow M-decay, which is thought to be essential for the phototaxis function of SRIs, has been reported previously [Suzuki, D., et al. (2009) J. Mol. Biol.392, 48-62]. Here the effects of the anion binding on the structure and structural changes of SRI during its photocycle are investigated by means of Fourier transform infrared (FTIR) spectroscopy and electrochemical experiments. Our results reveal that, among other things, the structural change and proton movement of a characteristic amino acid residue, Asp102 in SrSRI, is suppressed by the binding of an anion in its vicinity, both in the K- and M-intermediate. The presence of this anion also effects the extent of chromophore distrotion, and tentative results indicate an influence on the number and/or properties of internal water molecules. In addition, a photoinduced proton transfer could only be observed in the absence of the bound anion. Possible proton movement pathways, including the residues Asp102 and the putative Cl binding site His131, are discussed. In conclusion, the results show that the anion binding to SRI is not only important for the color tuning, and for controlling the photocycle kinetics, but also induces some structural changes which facilitate the observed properties.

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Year:  2012        PMID: 23062114     DOI: 10.1021/bi3009592

Source DB:  PubMed          Journal:  Biochemistry        ISSN: 0006-2960            Impact factor:   3.162


  2 in total

1.  Retinal chromophore structure and Schiff base interactions in red-shifted channelrhodopsin-1 from Chlamydomonas augustae.

Authors:  John I Ogren; Sergey Mamaev; Daniel Russano; Hai Li; John L Spudich; Kenneth J Rothschild
Journal:  Biochemistry       Date:  2014-06-16       Impact factor: 3.162

2.  Functional importance of the oligomer formation of the cyanobacterial H+ pump Gloeobacter rhodopsin.

Authors:  Azusa Iizuka; Kousuke Kajimoto; Tomotsumi Fujisawa; Takashi Tsukamoto; Tomoyasu Aizawa; Naoki Kamo; Kwang-Hwan Jung; Masashi Unno; Makoto Demura; Takashi Kikukawa
Journal:  Sci Rep       Date:  2019-07-24       Impact factor: 4.379

  2 in total

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