Structure-function relationships of vitamin D including ligand recognition by the vitamin D receptor

被引:77
作者
Yamada, S [1 ]
Shimizu, M [1 ]
Yamamoto, K [1 ]
机构
[1] Tokyo Med & Dent Univ, Inst Biomat & Bioengn, Chiyoda Ku, Tokyo 1010062, Japan
关键词
vitamin D; structure-function relationship; vitamin D receptor; conformational analysis; nuclear receptor;
D O I
10.1002/med.10023
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
First, the general structure and function of nuclear receptors (NRs) are described briefly to help our understanding of the mechanism of action of vitamin D mediated by the vitamin D receptor (VDR), a member of the NRs. Then we discuss the structure-function relationship (SFR) of vitamin D on the basis of ligand structures and the interaction of the ligand with the VDR. The SFR of vitamin D side chain analogs is discussed extensively in terms of our active space group concept, which was derived from conformational analyses of the side chains of vitamin D analogs and from studies with conformationally restricted 22-methyl-1,25-(OH)(2)D-3 isomers. The mobile area of the side chain of vitamin D can be grouped into five regions (E, G, EA, EG, and F), and the SFR has been analyzed in terms of these spatial regions. The SFR of ligand/VDR interaction is discussed on the basis of the crystal structure of VDR-LBD(Delta165-215), docking of various vitamin D ligands into the ligand binding pocket (LBP) of the VDR, and functional analysis of amino acids lining the LBP. Finally, we discuss total SFR, combining the results of the two approaches, and future aspects of structure-based design of vitamin D analogs. (C) 2002 Wiley Periodicals, Inc.
引用
收藏
页码:89 / 115
页数:27
相关论文
共 103 条
  • [1] SYNTHETIC ANALOGS OF VITAMIN-D3 WITH AN OXYGEN ATOM IN THE SIDE-CHAIN SKELETON - A TRAIL OF THE DEVELOPMENT OF VITAMIN-D COMPOUNDS WHICH EXHIBIT POTENT DIFFERENTIATION-INDUCING ACTIVITY WITHOUT INDUCING HYPERCALCEMIA
    ABE, J
    MORIKAWA, M
    MIYAMOTO, K
    KAIHO, SI
    FUKUSHIMA, M
    MIYAURA, C
    ABE, E
    SUDA, T
    NISHII, Y
    [J]. FEBS LETTERS, 1987, 226 (01) : 58 - 62
  • [2] CLONING AND EXPRESSION OF FULL-LENGTH CDNA-ENCODING HUMAN VITAMIN-D RECEPTOR
    BAKER, AR
    MCDONNELL, DP
    HUGHES, M
    CRISP, TM
    MANGELSDORF, DJ
    HAUSSLER, MR
    PIKE, JW
    SHINE, J
    OMALLEY, BW
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (10) : 3294 - 3298
  • [3] Human 25-hydroxyvitamin D3-24-hydroxylase, a multicatalytic enzyme
    Beckman, MJ
    Tadikonda, P
    Werner, E
    Prahl, J
    Yamada, S
    DeLuca, HF
    [J]. BIOCHEMISTRY, 1996, 35 (25) : 8465 - 8472
  • [4] BINDERUP E, 1991, VITAMIN D, P192
  • [5] EFFECTS OF A NOVEL VITAMIN-D ANALOG MC-903 ON CELL-PROLIFERATION AND DIFFERENTIATION INVITRO AND ON CALCIUM-METABOLISM INVIVO
    BINDERUP, L
    BRAMM, E
    [J]. BIOCHEMICAL PHARMACOLOGY, 1988, 37 (05) : 889 - 895
  • [6] 20-EPI-VITAMIN-D3 ANALOGS - A NOVEL CLASS OF POTENT REGULATORS OF CELL-GROWTH AND IMMUNE-RESPONSES
    BINDERUP, L
    LATINI, S
    BINDERUP, E
    BRETTING, C
    CALVERLEY, M
    HANSEN, K
    [J]. BIOCHEMICAL PHARMACOLOGY, 1991, 42 (08) : 1569 - 1575
  • [7] 25-HYDROXYCHOLECALCIFEROL . A BIOLOGICALLY ACTIVE METABOLITE OF VITAMIN D3
    BLUNT, JW
    DELUCA, HF
    SCHNOES, HK
    [J]. BIOCHEMISTRY, 1968, 7 (10) : 3317 - &
  • [8] Novel nonsecosteroidal vitamin D mimics exert VDR-modulating activities with less calcium mobilization than 1,25-dihydroxyvitamin D3
    Boehm, MF
    Fitzgerald, P
    Zou, AH
    Elgort, MG
    Bischoff, ED
    Mere, L
    Mais, DE
    Bissonnette, RP
    Heyman, RA
    Nadzan, AM
    Reichman, M
    Allegretto, EA
    [J]. CHEMISTRY & BIOLOGY, 1999, 6 (05): : 265 - 275
  • [9] STRUCTURE-FUNCTION-RELATIONSHIPS IN THE VITAMIN-D ENDOCRINE SYSTEM
    BOUILLON, R
    OKAMURA, WH
    NORMAN, AW
    [J]. ENDOCRINE REVIEWS, 1995, 16 (02) : 200 - 257
  • [10] BOUILLON R, 1993, J BONE MINER RES, V8, P1009