The Sigma Enigma: In Vitro/in Silico Site-Directed Mutagenesis Studies Unveil σ1 Receptor Ligand Binding

被引:44
|
作者
Brune, S. [1 ]
Schepmann, D. [1 ]
Klempnauer, K-H. [2 ]
Marson, D. [3 ]
Dal Col, V. [3 ]
Laurini, E. [3 ]
Fermeglia, M. [3 ]
Wuensch, B. [1 ]
Pricl, S. [3 ,4 ]
机构
[1] Univ Munster, Inst Pharmazeut & Med Chem, D-48149 Munster, Germany
[2] Univ Munster, Inst Biochem, D-48149 Munster, Germany
[3] Univ Trieste, DEA, Mol Simulat Engn MOSE Lab, I-34127 Trieste, Italy
[4] Univ Trieste, Natl Interuniv Consortium Mat Sci & Technol INSTM, Res Unit MOSE DEA, Trieste, Italy
关键词
AMINO-ACID-RESIDUES; MOLECULAR-DYNAMICS; GENERALIZED BORN; HOMOLOGY MODEL; SIMULATIONS; EXPRESSION; DOMAIN; BRAIN; PHARMACOLOGY; STABILITY;
D O I
10.1021/bi401575g
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
The sigma(1) receptor is an integral membrane protein that shares no homology with other receptor systems, has no unequivocally identified natural ligands, but appears to play critical roles in a wide variety of cell functions. While the number of reports of the possible functions of the sigma(1) receptor is increasing, almost no information about the three-dimensional structure of the receptor and/or possible modes of interaction of the sigma(1) protein with its ligands have been described. Here we performed an in vitro/in silico investigation to analyze the molecular interactions of the sigma(1) receptor with its prototypical agonist (+)-pentazocine. Accordingly, 23 mutant a, isoforms were generated, and their interactions with (+)-pentazocine were determined experimentally. All direct and/or indirect effects exerted by the mutant residues on the receptor-agonist interactions were reproduced and rationalized in silk, thus shining new light on the three-dimensional structure of the sigma(1) receptor and its ligand binding site.
引用
收藏
页码:2993 / 3003
页数:11
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