Intracellular lipid-binding proteins and their genes

被引:190
作者
Bernlohr, DA
Simpson, MA
Hertzel, AV
Banaszak, LJ
机构
[1] UNIV MINNESOTA, SCH MED, INST HUMAN GENET, ST PAUL, MN 55108 USA
[2] UNIV MINNESOTA, SCH MED, DEPT BIOCHEM, ST PAUL, MN 55108 USA
关键词
fatty acids; carrier proteins; peroxisome proliferator-activated receptors; dietary fat; gene expression;
D O I
10.1146/annurev.nutr.17.1.277
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
Intracellular lipid-binding proteins are a family of low-molecular-weight single-chain polypeptides that form 1:1 complexes with fatty acids, retinoids, or other hydrophobic ligands. These proteins are products of a large multigene family of unlinked loci distributed throughout the genome. Each lipid-binding protein exhibits a distinctive pattern of tissue distribution. Transcriptional control, regulated by a combination of peroxisome proliferator activated receptors and CCAAT/enhancer-binding proteins, allows for a variety of both cell and tissue-specific expression patterns. In some cells, fatty acids increase the expression of the lipid-binding protein genes. Fatty acids, or their metabolites, are activators of the peroxisome proliferator-activated receptor family of transcription factors. Therefore, as the concentration of lipid in the diet increases, the expression of lipid-binding proteins coordinately increases. As revealed by X-ray crystallography, the lipid-binding proteins fold into beta-barrels, forming a large internal water-filled cavity. Fatty acid ligands are bound within the cavity, occupying only about one-third of the accessible volume. The bound fatty acid is stabilized via a combination of enthalpic and entropic forces that govern ligand affinity and selectivity. Cytoplasmic lipid-binding proteins are the intracellular receptors for hydrophobic ligands, delivering them to the appropriate site for use as metabolic fuels and regulatory agents.
引用
收藏
页码:277 / 303
页数:27
相关论文
共 135 条
  • [1] AN AMINO-ACID SUBSTITUTION IN THE HUMAN INTESTINAL FATTY-ACID-BINDING PROTEIN IS ASSOCIATED WITH INCREASED FATTY-ACID-BINDING, INCREASED FAT OXIDATION, AND INSULIN-RESISTANCE
    BAIER, LJ
    SACCHETTINI, JC
    KNOWLER, WC
    EADS, J
    PAOLISSO, G
    TATARANNI, PA
    MOCHIZUKI, H
    BENNETT, PH
    BOGARDUS, C
    PROCHAZKA, M
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1995, 95 (03) : 1281 - 1287
  • [2] A polymorphism in the human intestinal fatty acid binding protein alters fatty acid transport across Caco-2 cells
    Baier, LJ
    Bogardus, C
    Sacchettini, JC
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (18) : 10892 - 10896
  • [3] BANASZAK L, 1994, ADV PROTEIN CHEM, V45, P89
  • [4] THE CELLULAR FATTY-ACID BINDING-PROTEINS - ASPECTS OF STRUCTURE, REGULATION, AND FUNCTION
    BASS, NM
    [J]. INTERNATIONAL REVIEW OF CYTOLOGY-A SURVEY OF CELL BIOLOGY, 1988, 111 : 143 - 184
  • [5] BASS NM, 1985, J BIOL CHEM, V260, P1432
  • [6] BASS NM, 1990, MOL CELL BIOCHEM, V98, P167
  • [7] BASS NM, 1985, J BIOL CHEM, V260, P9603
  • [8] GENE CLOSING, OVERPRODUCTION AND PURIFICATION OF A FUNCTIONALLY ACTIVE CYTOPLASMIC FATTY-ACID-BINDING PROTEIN (SJ-FABP(C)) FROM THE HUMAN BLOOD FLUKE SCHISTOSOMA-JAPONICUM
    BECKER, MM
    KALINNA, BH
    WAINE, GJ
    MCMANUS, DP
    [J]. GENE, 1994, 148 (02) : 321 - 325
  • [9] BENNING MM, 1992, J MOL BIOL, V228, P208
  • [10] TISSUE SPECIFIC EXPRESSION OF P422 PROTEIN, A PUTATIVE LIPID CARRIER, IN MOUSE ADIPOCYTES
    BERNLOHR, DA
    DOERING, TL
    KELLY, TJ
    LANE, MD
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1985, 132 (02) : 850 - 855