SYNTHESIS OF HIGH SPECIFIC ACTIVITY [H-3] 9-CIS-RETINOIC ACID AND ITS APPLICATION FOR IDENTIFYING RETINOIDS WITH UNUSUAL BINDING-PROPERTIES

被引:93
作者
BOEHM, MF
MCCLURG, MR
PATHIRANA, C
MANGELSDORF, D
WHITE, SK
HEBERT, J
WINN, D
GOLDMAN, ME
HEYMAN, RA
机构
[1] LIGAND PHARMACEUT INC,DEPT CELL BIOL,SAN DIEGO,CA 92121
[2] LIGAND PHARMACEUT INC,DEPT NEW LEADS DISCOVERY,SAN DIEGO,CA 92121
[3] UNIV TEXAS,SW MED CTR,HOWARD HUGHES MED INST,DEPT PHARMACOL,DALLAS,TX 75235
关键词
D O I
10.1021/jm00029a013
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
all-trans-Retinoic acid is known to bind to the retinoic acid receptors (RARs) resulting in an increase in their transcriptional activity. In contrast, recently identified 9-cis-retinoic acid (9-cis-RA), which is an additional endogenous RA isomer, is capable of binding to both RARs and retinoid X receptors (RXRs). These distinct properties have raised questions as to the biological role governed by these two retinoic acid isomers and the set of target genes that they regulate. Herein, we report the synthesis of high specific activity [H-3]-9-cis-RA and its application to study the ligand-binding properties of the various retinoid receptor subtypes. We examined the binding properties of RARs and RXRs for a series of synthetic retinoids and compared the ligand-binding properties of these arotinoid analogs with their ability to regulate gene expression via the retinoid receptors in a cotransfection assay. The utilization of the [3H]-9-cis-RA competitive binding assay and the cotransfection assay has made it possible to rapidly identify important structural features of retinoids leading to increased selectivity for either the RAR or RXR receptor subtypes.
引用
收藏
页码:408 / 414
页数:7
相关论文
共 35 条
  • [1] ALLEGRETTO EA, IN PRESS J BIOL CHEM
  • [2] RETINOIC ACID RECEPTORS AND RETINOID X-RECEPTORS - INTERACTIONS WITH ENDOGENOUS RETINOIC ACIDS
    ALLENBY, G
    BOCQUEL, MT
    SAUNDERS, M
    KAZMER, S
    SPECK, J
    ROSENBERGER, M
    LOVEY, A
    KASTNER, P
    GRIPPO, JF
    CHAMBON, P
    LEVIN, AA
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (01) : 30 - 34
  • [3] ANDRE H, 1990, J CHEM SOC CHEM COMM, V8, P627
  • [4] ANDRES H, 1992, SYNTHESIS AND APPLICATIONS OF ISOTOPICALLY LABELLED COMPOUNDS 1991, P40
  • [5] INTERACTION OF GLUCOCORTICOID ANALOGS WITH THE HUMAN GLUCOCORTICOID RECEPTOR
    BERGER, TS
    PARANDOOSH, Z
    PERRY, BW
    STEIN, RB
    [J]. JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY, 1992, 41 (3-8) : 733 - 738
  • [6] SYNTHESIS OF COMPOUNDS CONTAINING THE ISOPRENE UNIT - STEREOSPECIFIC SYNTHESIS OF BETA-IONILIDENEACETIC ACID AND DEHYDRO-BETA-IONILIDENEACETIC ACID, A KEY INTERMEDIATE TO ABSCISIC-ACID
    CAINELLI, G
    CARDILLO, G
    ORENA, M
    [J]. JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1, 1979, (06): : 1597 - 1599
  • [7] CARPENTER M, 1959, Patent No. 2897237
  • [8] DAVIS PL, COMMUNICATION
  • [9] C-13-NMR - STUDY OF CIS-TRANS ISOMERIC VITAMINS-A, CAROTENOIDS AND RELATED COMPOUNDS
    ENGLERT, G
    [J]. HELVETICA CHIMICA ACTA, 1975, 58 (08) : 2367 - 2390
  • [10] EVANS RM, 1836, Patent No. 11214