An integrated view on the role of receptor mosaics at perisynaptic level: focus on adenosine A2A, dopamine D2, cannabinoid CB1, and metabotropic glutamate mGlu5 receptors

被引:29
|
作者
Agnati, Luigi F. [1 ]
Guidolin, Diego [2 ]
Albertin, Giovanna [2 ]
Trivello, Elena [3 ]
Ciruela, Francisco [4 ]
Genedani, Susanna [3 ]
Tarakanov, Alexander [5 ]
Fuxe, Kjell [6 ]
机构
[1] IRCCS San Camillo, Lido Venezia, Italy
[2] Univ Padua, Dept Human Anat & Physiol, Padua, Italy
[3] Univ Modena & Reggio Emilia, Dept Biomed Sci, Modena, Italy
[4] IDIBELL Univ Barcelona, Fac Med, Dept Patol & Terapeut Expt, Unitat Farmacol, Barcelona, Spain
[5] Russian Acad Sci, St Petersburg Inst Informat & Automat, St Petersburg 196140, Russia
[6] Karolinska Inst, Dept Neurosci, Stockholm, Sweden
关键词
Receptor-receptor interactions; receptor mosaics; hub receptor; receptor biochemical similarity; horizontal molecular networks; bioinformatics; PROTEIN INTERACTION SITES; HIGHER-ORDER OLIGOMERS; D2; RECEPTORS; BINDING CHARACTERISTICS; CONCURRENT STIMULATION; HOT-SPOTS; PREDICTION; RAT; MODULATION; ACTIVATION;
D O I
10.3109/10799893.2010.487492
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 available evidence for receptor-receptor interactions between adenosine A(2A), dopamine D-2, cannabinoid CB1, and metabotropic glutamate mGlu(5) receptors (A(2A), D-2, CB1, and mGlu(5), respectively) is revised under the "receptor mosaic" perspective. Furthermore, the concept of "hub receptor" is defined in accordance with informatics and it is tentatively illustrated in the case of the hypothesized tetramer formed by the above mentioned receptors. On the basis of some biochemical features of the four receptors and of a bioinformatics analysis, an objective deduction of their "similarity" has been obtained. To this aim the Canberra, Euclidean and Chebyshev multivariate distance metrics have been used. It is interesting to note that A(2A) and D-2 are the most different ones, while CB1 and mGlu(5) are the most similar ones among the four receptors analyzed. Finally, by means of a bioinformatics analysis based on different approaches the possible binding sites mediating G-protein-coupled receptor (GPCR) interactions have been indicated. It is interesting to note that in some instances accordance has been found between the bioinformatics indications and the available experimental data.
引用
收藏
页码:355 / 369
页数:15
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