Literature DB >> 10698637

Theoretical study on mutation-induced activation of the luteinizing hormone receptor.

F Fanelli1.   

Abstract

Here, three-dimensional model building and molecular dynamics simulations of the luteinizing hormone receptor have been employed to generate hypotheses about the molecular mechanisms underlying the activation of the receptor induced by naturally occurring activating mutations. The comparative analysis of the wild-type receptor and of 16 constitutively active or inactive mutants has been instrumental in inferring the structural/dynamic features which could characterize the inactive and the active forms of the receptor. These features have been also employed for predicting the functional behavior of new receptor mutants. The results of this study might provide a structural framework to interpret the pathological effects induced by mutations of the luteinizing hormone receptor. In addition, the proposed theoretical model could be useful for engineering new mutations or ligands able to modulate receptor function. Copyright 2000 Academic Press.

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Year:  2000        PMID: 10698637     DOI: 10.1006/jmbi.2000.3516

Source DB:  PubMed          Journal:  J Mol Biol        ISSN: 0022-2836            Impact factor:   5.469


  9 in total

1.  Key issues in the computational simulation of GPCR function: representation of loop domains.

Authors:  E L Mehler; X Periole; S A Hassan; H Weinstein
Journal:  J Comput Aided Mol Des       Date:  2002-11       Impact factor: 3.686

2.  Bioluminescence resonance energy transfer studies reveal constitutive dimerization of the human lutropin receptor and a lack of correlation between receptor activation and the propensity for dimerization.

Authors:  Rongbin Guan; Xiuyan Feng; Xueqing Wu; Meilin Zhang; Xuesen Zhang; Terence E Hébert; Deborah L Segaloff
Journal:  J Biol Chem       Date:  2009-01-15       Impact factor: 5.157

Review 3.  Constitutive activation of G protein-coupled receptors and diseases: insights into mechanisms of activation and therapeutics.

Authors:  Ya-Xiong Tao
Journal:  Pharmacol Ther       Date:  2008-08-09       Impact factor: 12.310

Review 4.  Insights learned from L457(3.43)R, an activating mutant of the human lutropin receptor.

Authors:  Ana Claudia Latronico; Deborah L Segaloff
Journal:  Mol Cell Endocrinol       Date:  2006-10-18       Impact factor: 4.102

5.  A cell surface inactive mutant of the human lutropin receptor (hLHR) attenuates signaling of wild-type or constitutively active receptors via heterodimerization.

Authors:  Meilin Zhang; Xiuyan Feng; Rongbin Guan; Terence E Hébert; Deborah L Segaloff
Journal:  Cell Signal       Date:  2009-07-16       Impact factor: 4.315

6.  The formation of a salt bridge between helices 3 and 6 is responsible for the constitutive activity and lack of hormone responsiveness of the naturally occurring L457R mutation of the human lutropin receptor.

Authors:  Meilin Zhang; Dario Mizrachi; Francesca Fanelli; Deborah L Segaloff
Journal:  J Biol Chem       Date:  2005-05-20       Impact factor: 5.157

Review 7.  A functional transmembrane complex: the luteinizing hormone receptor with bound ligand and G protein.

Authors:  D Puett; Y Li; G DeMars; K Angelova; F Fanelli
Journal:  Mol Cell Endocrinol       Date:  2006-10-23       Impact factor: 4.102

Review 8.  Inactive and active states and supramolecular organization of GPCRs: insights from computational modeling.

Authors:  Francesca Fanelli; Pier G De Benedetti
Journal:  J Comput Aided Mol Des       Date:  2006-09-29       Impact factor: 4.179

Review 9.  Structural aspects of luteinizing hormone receptor: information from molecular modeling and mutagenesis.

Authors:  Francesca Fanelli; David Puett
Journal:  Endocrine       Date:  2002-08       Impact factor: 3.633

  9 in total

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