RHODOSTOMIN, AN RGD-CONTAINING PEPTIDE EXPRESSED FROM A SYNTHETIC GENE IN ESCHERICHIA-COLI, FACILITATES THE ATTACHMENT OF HUMAN HEPATOMA-CELLS

被引:38
作者
CHANG, HH
HU, ST
HUANG, TF
CHEN, SH
LEE, YHW
LO, SCJ
机构
[1] NATL YANG MING MED COLL, GRAD INST MICROBIOL & IMMUNOL, TAIPEI, TAIWAN
[2] NATL YANG MING MED COLL, INST BIOCHEM, TAIPEI, TAIWAN
[3] NATL TAIWAN UNIV, INST PHARMACOL, TAIPEI, TAIWAN
[4] NATL CHENG KUNG UNIV, DEPT BIOL, TAINAN, TAIWAN
关键词
D O I
10.1006/bbrc.1993.1037
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
Rhodostomin (Rho) from snake venom, a potent inhibitor of platelet aggregation, contains 68 amino acids having an ROD sequence and 12 cysteine residues. A chemically synthesized Rho gene was cloned and expressed in Escherichia coli. The expression of Rho gene fused with the glutathione S-transferase (GST) gene was about 10-30% of total cell proteins. The Rho-fusion protein could be recognized by antibodies raised against either a native Rho peptide or a synthetic peptide. The purified GST-Rho coated on culture plates facilitated the attachment of human hepatoma cells, which was inhibitable by co-incubation with a synthetic hexapeptide GRGDSP but not with a related peptide of GRGESP, suggesting that the E. coli-expressed Rho-fusion protein was properly folded and biologically functional. © 1993 Academic Press, Inc.
引用
收藏
页码:242 / 249
页数:8
相关论文
共 24 条
  • [1] A COMMON PRECURSOR FOR A PUTATIVE HEMORRHAGIC PROTEIN AND RHODOSTOMIN, A PLATELET-AGGREGATION INHIBITOR OF THE VENOM OF CALLOSELASMA-RHODOSTOMA - MOLECULAR-CLONING AND SEQUENCE-ANALYSIS
    AU, LC
    HUANG, YB
    HUANG, TF
    TEH, GW
    LIN, HH
    CHOO, KB
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1991, 181 (02) : 585 - 593
  • [2] Blobel Carl P., 1992, Current Opinion in Cell Biology, V4, P760
  • [3] BUCK CA, 1987, ANNU REV CELL BIOL, V3, P179, DOI 10.1146/annurev.cellbio.3.1.179
  • [4] GOULD RJ, 1990, P SOC EXP BIOL MED, V195, P168, DOI 10.3181/00379727-195-43129B
  • [5] PREFERENTIAL CODON USAGE IN PROKARYOTIC GENES - THE OPTIMAL CODON ANTICODON INTERACTION ENERGY AND THE SELECTIVE CODON USAGE IN EFFICIENTLY EXPRESSED GENES
    GROSJEAN, H
    FIERS, W
    [J]. GENE, 1982, 18 (03) : 199 - 209
  • [6] EXPRESSION IN ESCHERICHIA-COLI OF A SYNTHETIC GENE CODING FOR HORSE HEART MYOGLOBIN
    GUILLEMETTE, JG
    MATSUSHIMAHIBIYA, Y
    ATKINSON, T
    SMITH, M
    [J]. PROTEIN ENGINEERING, 1991, 4 (05): : 585 - 592
  • [7] HUANG TF, 1987, J BIOL CHEM, V262, P16157
  • [8] HUANG TF, 1991, J BIOCHEM-TOKYO, V109, P328
  • [9] CHARACTERIZATION OF A POTENT PLATELET-AGGREGATION INHIBITOR FROM AGKISTRODON-RHODOSTOMA SNAKE-VENOM
    HUANG, TF
    WU, YJ
    OUYANG, C
    [J]. BIOCHIMICA ET BIOPHYSICA ACTA, 1987, 925 (03) : 248 - 257
  • [10] THE SCANNING MODEL FOR TRANSLATION - AN UPDATE
    KOZAK, M
    [J]. JOURNAL OF CELL BIOLOGY, 1989, 108 (02) : 229 - 241