The mechanism of proton translocation in respiratory complex I from molecular dynamics

Abstract

Respiratory complex I, the biggest enzyme of respiratory chain, plays a key role in energy production by the mitochondrial respiratory chain and has been implicated in many human neurodegenerative diseases. Recently, the crystal structure of respiratory complex I is reported. We perform 50 ns molecular dynamics simulations on the membrane domain of respiratory complex I under two hypothetical states (oxidized state and reduced state). We find that the density of water molecules in the trans-membrane domain under reduced state is bigger than that under oxidized state. The connecting elements (helix HL and β-hairpins-helix element) fluctuate stronger under reduced state than that under oxidized state, causing more internal water molecules and facilitating the proton conduction. The conformational changes of helix HL and the crucial charged residue Glu in TM5 play key roles in the mechanism of proton translocation. Our results illustrate the dynamic behavior and the potential mechanism of respiratory complex I, which provides the structural basis for drug design of respiratory complex I.

• Molecular dynamics
• membrane protein
• protein structure

Declaration of interest

This work is supported by the National Basic Research Program of China (973 Program, grant no. 2012CB932400), the National Natural Science Foundation of China (grant no. 91233115, 21273158, 21303112 and 91227201), Natural Science Foundation of Jiangsu Province (grant no. BK20130291), a Project Funded by the Priority Academic Program Development of Jiangsu Higher Education Institutions (PAPD). This is also a project supported by the Fund for Innovative Research Teams of Jiangsu Higher Education Institutions.