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  4. Rhodopsin from Haloquadratum walsbyi is a light-driven magnesium transporter
 
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Rhodopsin from Haloquadratum walsbyi is a light-driven magnesium transporter

Journal
Nature Communications
Journal Volume
16
Journal Issue
1
Start Page
Article number 4472
ISSN
2041-1723
Date Issued
2025-05-14
Author(s)
Ko, Ling-Ning
Lim, Guo Zhen
Chen, Jui-Chien
Ko, Ta
Li, Guan-Yi
CHII-SHEN YANG  
DOI
10.1038/s41467-025-59795-y
URI
https://www.scopus.com/record/display.uri?eid=2-s2.0-105005116266&origin=resultslist
https://scholars.lib.ntu.edu.tw/handle/123456789/730004
Abstract
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.
Publisher
Springer Science and Business Media LLC
Type
journal article

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