| Mechanism of Signal Propagation upon Retinal Isomerization: Insights from Molecular Dynamics Simulations of Rhodopsin Restrained by Normal Modes Biophysical Journal, Volume 95, Issue 2, 15 July 2008, Pages 789-803 Basak Isin, Klaus Schulten, Emad Tajkhorshid and Ivet Bahar Abstract As one of the best studied members of the pharmaceutically relevant family of G-protein-coupled receptors, rhodopsin serves as a prototype for understanding the mechanism of G-protein-coupled receptor activation. Here, we aim at exploring functionally relevant conformational changes and signal transmission mechanisms involved in its photoactivation brought about through a photoisomerization of retinal. For this exploration, we propose a molecular dynamics simulation protocol that utilizes normal modes derived from the anisotropic network model for proteins. Deformations along multiple low-frequency modes of motion are used to efficiently sample collective conformational changes in the presence of explicit membrane and water environment, consistent with interresidue interactions. We identify two highly stable regions in rhodopsin, one clustered near the chromophore, the other near the cytoplasmic ends of transmembrane helices H1, H2, and H7. Due to redistribution of interactions in the neighborhood of retinal upon stabilization of the form, local structural rearrangements in the adjoining H3–H6 residues are efficiently propagated to the cytoplasmic end of these particular helices. In the structures obtained by our simulations, all- retinal interacts with Cys on H4 and Phe on H5, which were not accessible in the dark state, and exhibits stronger interactions with H5, while some of the contacts made (in the form) with H6 are lost. Abstract | Full Text | PDF (2019 kb) |
| The Signaling Pathway of Rhodopsin Structure, Volume 15, Issue 5, 16 May 2007, Pages 611-623 Yifei Kong and Martin Karplus Summary The signal-transduction mechanism of rhodopsin was studied by molecular dynamics (MD) simulations of the high-resolution, inactive structure in an explicit membrane environment. The simulations were employed to calculate equal-time correlations of the fluctuating interaction energy of residue pairs. The resulting interaction-correlation matrix was used to determine a network that couples retinal to the cytoplasmic interface, where transducin binds. Two highly conserved motifs, D(E)RY and NPxxY, were found to have strong interaction correlation with retinal. MD simulations with restraints on each transmembrane helix indicated that the major signal-transduction pathway involves the interdigitating side chains of helices VI and VII. The functional roles of specific residues were elucidated by the calculated effect of retinal isomerization from 11- to all- on the residue-residue interaction pattern. It is suggested that Glu134 may act as a “signal amplifier” and that Asp83 may introduce a threshold to prevent background noise from activating rhodopsin. Summary | Full Text | PDF (2260 kb) |
| Solution Structure of the Tctex1 Dimer Reveals a Mechanism for Dynein-Cargo Interactions Structure, Volume 13, Issue 2, 1 February 2005, Pages 213-223 Hongwei Wu, Mark W. Maciejewski, Sachiko Takebe and Stephen M. King Summary Tctex1 is a light chain found in both cytoplasmic and flagellar dyneins and is involved in many fundamental cellular activities, including rhodopsin transport within photoreceptors, and may function in the non-Mendelian transmission of haplotypes in mice. Here, we present the NMR solution structure for the Tctex1 dimer from axonemal inner dynein arm I1. Structural comparisons reveal a strong similarity with the LC8 dynein light chain dimer, including formation of a strand-switched β sheet interface. Analysis of the Tctex1 structure enables the dynein intermediate chain binding site to be identified and suggests a mechanism by which cargo proteins might be attached to this microtubule motor complex. Comparison with the alternate dynein light chain rp3 reveals how the specificity of dynein-cargo interactions mediated by these dynein components is achieved. In addition, this structure provides insight into the consequences of the mutations found in the haplotype forms of this protein. Summary | Full Text | PDF (866 kb) |
Copyright © 1995 The Biophysical Society. All rights reserved.
Biophysical Journal, Volume 69, Issue 6, 2419-2442, 1 December 1995
doi:10.1016/S0006-3495(95)80112-8
Research Article
P. Herzyk and R.E. Hubbard
Department of Chemistry, University of York, Heslington, United Kingdom. pavel@yorvic.york.ac.uk
A rule-based automated method is presented for modeling the structures of the seven transmembrane helices of G-protein-coupled receptors. The structures are generated by using a simulated annealing Monte Carlo procedure that positions and orients rigid helices to satisfy structural restraints. The restraints are derived from analysis of experimental information from biophysical studies on native and mutant proteins, from analysis of the sequences of related proteins, and from theoretical considerations of protein structure. Calculations are presented for two systems. The method was validated through calculations using appropriate experimental information for bacteriorhodopsin, which produced a model structure with a root mean square (rms) deviation of 1.87 A from the structure determined by electron microscopy. Calculations are also presented using experimental and theoretical information available for bovine rhodopsin to assign the helices to a projection density map and to produce a model of bovine rhodopsin that can be used as a template for modeling other G-protein-coupled receptors.