8TUP

Cryo-EM structure of the human MRS2 magnesium channel under Mg2+-free condition

8TUP の概要

• エントリーDOI: 10.2210/pdb8tup/pdb
• 関連するPDBエントリー: 8TUL
• EMDBエントリー: 41624 41628
• 分子名称: Magnesium transporter MRS2 homolog, mitochondrial, MAGNESIUM ION (3 entities in total)
• 機能のキーワード: magnesium, ion channel, membrane protein, metal transport, ion translocation, divalent ion, pentamer
• 由来する生物種: Homo sapiens (human)
• タンパク質・核酸の鎖数: 5
• 化学式量合計: 256940.50

構造登録者

Lai, L.T.F.,Balaraman, J.,Zhou, F.,Matthies, D. (登録日: 2023-08-16, 公開日: 2023-09-13, 最終更新日: 2024-05-01)

主引用文献

Lai, L.T.F.,Balaraman, J.,Zhou, F.,Matthies, D.
Cryo-EM structures of human magnesium channel MRS2 reveal gating and regulatory mechanisms.
Nat Commun, 14:7207-7207, 2023

PubMed Abstract: Magnesium ions (Mg) play an essential role in cellular physiology. In mitochondria, protein and ATP synthesis and various metabolic pathways are directly regulated by Mg. MRS2, a magnesium channel located in the inner mitochondrial membrane, mediates the influx of Mg into the mitochondrial matrix and regulates Mg homeostasis. Knockdown of MRS2 in human cells leads to reduced uptake of Mg into mitochondria and disruption of the mitochondrial metabolism. Despite the importance of MRS2, the Mg translocation and regulation mechanisms of MRS2 are still unclear. Here, using cryo-EM we report the structures of human MRS2 in the presence and absence of Mg at 2.8 Å and 3.3 Å, respectively. From the homo-pentameric structures, we identify R332 and M336 as major gating residues, which are then tested using mutagenesis and two cellular divalent ion uptake assays. A network of hydrogen bonds is found connecting the gating residue R332 to the soluble domain, potentially regulating the gate. Two Mg-binding sites are identified in the MRS2 soluble domain, distinct from the two sites previously reported in CorA, a homolog of MRS2 in prokaryotes. Altogether, this study provides the molecular basis for understanding the Mg translocation and regulatory mechanisms of MRS2.

PubMed: 37938562
DOI: 10.1038/s41467-023-42599-3

実験手法

ELECTRON MICROSCOPY (3.3 Å)