<p>The functionally unknown Middle rhodopsin (HwMR) is a microbial rhodopsin (mRho) identified in <i>Haloquadratum walsbyi</i>, an archaeon that thrives in a 2 M MgCl<sub>2</sub> environment harmful to most other microorganisms. HwMR shares conserved and functionally critical residues with both bacteriorhodopsin (BR), a proton pump, and sensory rhodopsin II (SRII), which mediates phototaxis, even though HwMR exerts neither function. We previously reported HwMR as a unique mRho found to associate with Mg<sup>2+</sup>. Here, we show that HwMR can sense environmental Mg<sup>2+</sup> concentration via the D84 residue according to characteristic maximum absorption wavelength shift, photocycle kinetics, and Mg<sup>2+</sup> titration assay. X-ray crystallography of the wild-type HwMR and its D84N mutant produced two HwMR atomic structure models. Omit maps analysis of the wild-type HwMR model revealed D84 as a Mg<sup>2+</sup> binding site. On the cytoplasmic side, omit maps also revealed Mg<sup>2+</sup> association with T216. Both Mg<sup>2+</sup> sites were absent in the D84N mutant. A cell-based light-driven conductivity assay provided evidence to propose that HwMR is an inward magnesium transporter, with D84 as the primary binding site and T216 as the transportation stabilizing site. A sequential model was proposed to illustrate Mg<sup>2+</sup> transportation in HwMR.</p>

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Rhodopsin from Haloquadratum walsbyi is a light-driven magnesium transporter

  • Ling-Ning Ko,
  • Guo Zhen Lim,
  • Jui-Chien Chen,
  • Ta Ko,
  • Guan-Yi Li,
  • Chii-Shen Yang

摘要

The functionally unknown Middle rhodopsin (HwMR) is a microbial rhodopsin (mRho) identified in Haloquadratum walsbyi, an archaeon that thrives in a 2 M MgCl2 environment harmful to most other microorganisms. HwMR shares conserved and functionally critical residues with both bacteriorhodopsin (BR), a proton pump, and sensory rhodopsin II (SRII), which mediates phototaxis, even though HwMR exerts neither function. We previously reported HwMR as a unique mRho found to associate with Mg2+. Here, we show that HwMR can sense environmental Mg2+ concentration via the D84 residue according to characteristic maximum absorption wavelength shift, photocycle kinetics, and Mg2+ titration assay. X-ray crystallography of the wild-type HwMR and its D84N mutant produced two HwMR atomic structure models. Omit maps analysis of the wild-type HwMR model revealed D84 as a Mg2+ binding site. On the cytoplasmic side, omit maps also revealed Mg2+ association with T216. Both Mg2+ sites were absent in the D84N mutant. A cell-based light-driven conductivity assay provided evidence to propose that HwMR is an inward magnesium transporter, with D84 as the primary binding site and T216 as the transportation stabilizing site. A sequential model was proposed to illustrate Mg2+ transportation in HwMR.