A METHOD FOR BINDING PARAMETERS ESTIMATION OF A1 ADENOSINE RECEPTOR SUBTYPE - A PRACTICAL APPROACH

被引:21
作者
CASADO, V
MARTI, T
FRANCO, R
LLUIS, C
MALLOL, J
CANELA, EI
机构
[1] Departament de Bioquímica i Fisiologia, Facultat de Química, Universitat de Barcelona, 08071 Barcelona, Catalunya, Martí i Franquès
关键词
Adenosine receptor - Binding capacities - Binding parameter - Equilibrium parameters - Experimental determination - Non-specific binding - Physiological ligands - Saturation experiments;
D O I
10.1016/0003-2697(90)90022-2
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Working with pig brain striatum in which A1 and A2 adenosine receptor subtypes coexist, we describe an uncomplicated method for unequivocally obtaining the equilibrium parameters (KD and binding capacity) of A1 receptor without interference from ligand binding to A2 receptor. Also, the equilibrium parameter estimation method we propose avoids the experimental determination of nonspecific binding by the inclusion of the corresponding unknown parameter in the function. This not only saves time but also avoids the use of expensive radioligands in saturation experiments. The method is suitable for any system with two different receptor subtypes for the same physiological ligand, and good estimates of the equilibrium parameters corresponding to the subtype displaying the higher affinity for the ligand can be obtained. © 1990.
引用
收藏
页码:117 / 123
页数:7
相关论文
共 35 条
[11]   5'-N-ETHYLCARBOXAMIDO[8-H-3]ADENOSINE BINDS TO 2 DIFFERENT ADENOSINE RECEPTORS IN MEMBRANES FROM THE CEREBRAL-CORTEX OF THE RAT [J].
FLORIO, C ;
TRAVERSA, U ;
VERTUA, R ;
PUPPINI, P .
NEUROPHARMACOLOGY, 1988, 27 (01) :85-94
[12]   HOW DOES ADENOSINE INHIBIT TRANSMITTER RELEASE [J].
FREDHOLM, BB ;
DUNWIDDIE, TV .
TRENDS IN PHARMACOLOGICAL SCIENCES, 1988, 9 (04) :130-134
[13]  
FREDHOLM BB, 1988, NEUROTRANSMITTERS CO, P437
[14]  
HAAS HL, 1988, NEUROTRANSMITTERS CO, P483
[15]   RA-ADENOSINE RECEPTORS IN HUMAN-PLATELETS - CHARACTERIZATION BY "5'-N-ETHYLCARBOXAMIDO[H-3]ADENOSINE BINDING IN RELATION TO ADENYLATE-CYCLASE ACTIVITY [J].
HUTTEMANN, E ;
UKENA, D ;
LENSCHOW, V ;
SCHWABE, U .
NAUNYN-SCHMIEDEBERGS ARCHIVES OF PHARMACOLOGY, 1984, 325 (03) :226-233
[16]   ADENOSINE RECEPTOR ALTERATIONS IN NERVOUS POINTER DOGS - A PRELIMINARY-REPORT [J].
KLEIN, E ;
MARANGOS, PJ ;
MONTGOMERY, P ;
BACHER, J ;
UHDE, TW .
CLINICAL NEUROPHARMACOLOGY, 1987, 10 (05) :462-469
[17]   1,3-DIPROPYL-8-CYCLOPENTYLXANTHINE (DPCPX) INHIBITION OF [H-3] N-ETHYLCARBOXAMIDOADENOSINE (NECA) BINDING ALLOWS THE VISUALIZATION OF PUTATIVE NON-A1 ADENOSINE RECEPTORS [J].
LEE, KS ;
REDDINGTON, M .
BRAIN RESEARCH, 1986, 368 (02) :394-398
[18]   SUBCLASSES OF EXTERNAL ADENOSINE RECEPTORS [J].
LONDOS, C ;
COOPER, DMF ;
WOLFF, J .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1980, 77 (05) :2551-2554
[19]   IDENTIFICATION AND REJECTION OF OUTLIERS IN ENZYME-KINETICS [J].
LOPEZCABRERA, A ;
CABRE, F ;
FRANCO, R ;
CANELA, EI .
INTERNATIONAL JOURNAL OF BIO-MEDICAL COMPUTING, 1988, 23 (1-2) :9-20
[20]  
LOSHE MJ, 1985, J NEUROCHEM, V45, P1761