Calcium binding to the purple membrane: A molecular dynamics study

• Published in: Proteins, structure, function, and bioinformatics Vol. 74; no. 3; pp. 669 - 681
• Main Authors: Wassenaar, Tsjerk A., Daura, Xavier, Padrós, Esteve, Mark, Alan E.
• Format: Journal Article
• Language: English
• Published: Hoboken Wiley Subscription Services, Inc., A Wiley Company 15.02.2009
• Subjects: Archaea; bacteriorhodopsin; Binding Sites; bond valence sum; Calcium - chemistry; Calcium - metabolism; cation binding; Computer Simulation; Crystallography, X-Ray; Glutamic Acid - genetics; Glutamic Acid - metabolism; Models, Molecular; Purple Membrane - chemistry; Purple Membrane - metabolism; Schiff Bases; simulation
• ISSN: 0887-3585; 1097-0134
• DOI: 10.1002/prot.22182

The purple membrane (PM) is a specialized membrane patch found in halophilic archaea, containing the photoreceptor bacteriorhodopsin (bR). It is long known that calcium ions bind to the PM, but their position and role remain elusive to date. Molecular dynamics simulations in conjunction with a highly detailed model of the PM have been used to investigate the stability of calcium ions placed at three proposed cation binding sites within bR, one near the Schiff base, one in the region of the proton release group, and one near Glu9. The simulations suggest that, of the sites investigated, the binding of calcium ions was most likely at the proton release group. Binding in the region of the Schiff base, while possible, was associated with significant changes in local geometry. Calcium ions placed near Glu9 in the interior of bR (simultaneously to a Ca2+ near the Schiff base and another one near the Glu194–Glu204 site) were not stable. The results obtained are discussed in relation to recent experimental observations and theoretical considerations. Proteins 2009. © 2008 Wiley‐Liss, Inc.