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

被引:42
作者
Fanelli, F [1 ]
机构
[1] Univ Modena & Reggio Emilia, Dipartimento Chim, I-41100 Modena, Italy
关键词
luteinizing hormone receptor; G proteins; receptor activation; molecular dynamics; constitutive activity;
D O I
10.1006/jmbi.2000.3516
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:1333 / 1351
页数:19
相关论文
共 87 条
[41]   NMR AND CIRCULAR-DICHROISM STUDIES OF SYNTHETIC PEPTIDES DERIVED FROM THE 3RD INTRACELLULAR LOOP OF THE BETA-ADRENOCEPTOR [J].
JUNG, H ;
WINDHABER, R ;
PALM, D ;
SCHNACKERZ, KD .
FEBS LETTERS, 1995, 358 (02) :133-136
[42]   Conformation of a beta-adrenoceptor-derived signal transducing peptide as inferred by circular dichroism and H-1 NMR spectroscopy [J].
Jung, H ;
Windhaber, R ;
Palm, D ;
Schnackerz, KD .
BIOCHEMISTRY, 1996, 35 (20) :6399-6405
[43]  
KARNIK SS, 1990, J BIOL CHEM, V265, P17520
[44]   Structure and function in rhodopsin: Rhodopsin mutants with a neutral amino acid at E134 have a partially activated conformation in the dark state [J].
Kim, JM ;
Altenbach, C ;
Thurmond, RL ;
Khorana, HG ;
Hubbell, WL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (26) :14273-14278
[45]  
KJELSBERG MA, 1992, J BIOL CHEM, V267, P1430
[46]   Single-cysteine substitution mutants at amino acid positions 55-75, the sequence connecting the cytoplasmic ends of helices I and II in rhodopsin: Reactivity of the sulfhydryl groups and their derivatives identifies a tertiary structure that changes upon light-activation [J].
Klein-Seetharaman, J ;
Hwa, J ;
Cai, KW ;
Altenbach, C ;
Hubbell, WL ;
Khorana, HG .
BIOCHEMISTRY, 1999, 38 (25) :7938-7944
[47]   A proposed structure for transmembrane segment 7 of G protein-coupled receptors incorporating an Asn-Pro/Asp-Pro motif [J].
Konvicka, K ;
Guarnieri, F ;
Ballesteros, JA ;
Weinstein, H .
BIOPHYSICAL JOURNAL, 1998, 75 (02) :601-611
[48]   The role of Asp(578) in maintaining the inactive conformation of the human lutropin/choriogonadotropin receptor [J].
Kosugi, S ;
Mori, T ;
Shenker, A .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (50) :31813-31817
[49]   CHARACTERIZATION OF HETEROGENEOUS MUTATIONS CAUSING CONSTITUTIVE ACTIVATION OF THE LUTEINIZING-HORMONE RECEPTOR IN FAMILIAL MALE PRECOCIOUS PUBERTY [J].
KOSUGI, S ;
VANDOP, C ;
GEFFNER, ME ;
RABL, W ;
CAREL, JC ;
CHAUSSAIN, JL ;
MORI, T ;
MERENDINO, JJ ;
SHENKER, A .
HUMAN MOLECULAR GENETICS, 1995, 4 (02) :183-188
[50]   A MISSENSE MUTATION IN THE 2ND TRANSMEMBRANE SEGMENT OF THE LUTEINIZING-HORMONE RECEPTOR CAUSES FAMILIAL MALE-LIMITED PRECOCIOUS PUBERTY [J].
KRAAIJ, R ;
POST, M ;
KREMER, H ;
MILGROM, E ;
EPPING, W ;
BRUNNER, HG ;
GROOTEGOED, JA ;
THEMMEN, APN .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1995, 80 (11) :3168-3172