The dopamine D4 receptor, the ultimate disordered protein

被引:25
作者
Woods, Amina S. [1 ]
机构
[1] NIDA IRP, NIH, Struct Biol Unit, Cellular Neurobiol Branch, Baltimore, MD 21224 USA
关键词
Dopamine D4 Receptor; Disordered proteins; AKAP; Heteromers; Adenosine A2A Receptor; ELECTROSTATIC INTERACTION; ADENOSINE A(2A); SH3; DOMAINS; HETEROMERIZATION; PREDICTION; COMPLEXITY; SEQUENCE; MOSAICS; NEURONS;
D O I
10.3109/10799893.2010.513842
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 human D4 dopamine receptor is a synaptic neurotransmitter receptor responsible for neuronal signaling in the mesolimbic system of the brain, an area of the brain that regulates emotion and complex behavior. Its structure makes it a very unusual and interesting G protein-coupled receptor (GPCR) as it has several polymorphic variants of its gene in the region encoding the third intracellular loop (IL3). This region contains from two to seven or more similar 48 base pair repeats. These repeats cause this protein to have a very high disorder index and this, in turn, makes it very interactive with other proteins. Among GPCRs in general, the unusually proline-rich IL3 is unique to the D4 receptor (D4R). We believe that, as in the D2R, this region of the receptor plays a role in it's interaction with other receptors.
引用
收藏
页码:331 / 336
页数:6
相关论文
共 29 条
[1]   Theoretical Considerations on the Topological Organization of Receptor Mosaics [J].
Agnati, Luigi Francesco ;
Fuxe, Kjell ;
Woods, Amina S. ;
Genedani, Susanna ;
Guidolin, Diego .
CURRENT PROTEIN & PEPTIDE SCIENCE, 2009, 10 (06) :559-569
[2]   Anatomical and physiological evidence for D1 and D2 dopamine receptor colocalization in neostriatal neurons [J].
Aizman, O ;
Brismar, H ;
Uhlén, P ;
Zettergren, E ;
Levey, AI ;
Forssberg, H ;
Greengard, P ;
Aperia, A .
NATURE NEUROSCIENCE, 2000, 3 (03) :226-230
[3]   Combining mass spectrometry and pull-down techniques for the study of receptor heteromerization.: Direct epitope-epitope electrostatic interactions between adenosine A2A and dopamine D2 receptors [J].
Ciruela, F ;
Burgueño, J ;
Casadó, V ;
Canals, M ;
Marcellino, D ;
Goldberg, SR ;
Bader, M ;
Fuxe, K ;
Agnati, LF ;
Lluis, C ;
Franco, R ;
Ferré, S ;
Woods, AS .
ANALYTICAL CHEMISTRY, 2004, 76 (18) :5354-5363
[4]  
Creighton T.E., 1993, PROTEINS, V2nd, P6
[5]  
Dunker AK, 2002, ADV PROTEIN CHEM, V62, P25
[6]   Intrinsically unstructured proteins and their functions [J].
Dyson, HJ ;
Wright, PE .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2005, 6 (03) :197-208
[7]   Building a new conceptual framework for receptor heteromers [J].
Ferre, Sergi ;
Baler, Ruben ;
Bouvier, Michel ;
Caron, Marc G. ;
Devi, Lakshmi A. ;
Durroux, Thierry ;
Fuxe, Kjell ;
George, Susan R. ;
Javitch, Jonathan A. ;
Lohse, Martin J. ;
Mackie, Ken ;
Milligan, Graeme ;
Pfleger, Kevin D. G. ;
Pin, Jean-Philippe ;
Volkow, Nora D. ;
Waldhoer, Maria ;
Woods, Amina S. ;
Franco, Rafael .
NATURE CHEMICAL BIOLOGY, 2009, 5 (03) :131-134
[8]   Intramembrane receptor-receptor interactions:: a novel principle in molecular medicine [J].
Fuxe, K. ;
Canals, M. ;
Torvinen, M. ;
Marcellino, D. ;
Terasmaa, A. ;
Genedani, S. ;
Leo, G. ;
Guidolin, D. ;
Diaz-Cabiale, Z. ;
Rivera, A. ;
Lundstrom, L. ;
Langel, U. ;
Narvaez, J. ;
Tanganelli, S. ;
Lluis, C. ;
Ferre, S. ;
Woods, A. ;
Franco, R. ;
Agnati, L. F. .
JOURNAL OF NEURAL TRANSMISSION, 2007, 114 (01) :49-75
[9]   Heterodimers and Receptor Mosaics of Different Types of G-Protein-Coupled Receptors [J].
Fuxe, Kjell ;
Marcellino, Daniel ;
Guidolin, Diego ;
Woods, Amina S. ;
Agnati, Luigi F. .
PHYSIOLOGY, 2008, 23 (06) :322-332
[10]   Protein disorder prediction: Implications for structural proteomics [J].
Linding, R ;
Jensen, LJ ;
Diella, F ;
Bork, P ;
Gibson, TJ ;
Russell, RB .
STRUCTURE, 2003, 11 (11) :1453-1459