High-performance affinity beads for identifying drug receptors

被引:217
作者
Shimizu, N
Sugimoto, K
Tang, JW
Nishi, T
Sato, I
Hiramoto, M
Aizawa, S
Hatakeyama, M
Ohba, R
Hatori, H
Yoshikawa, T
Suzuki, F
Oomori, A
Tanaka, H
Kawaguchi, H
Watanabe, H
Handa, H [1 ]
机构
[1] Tokyo Inst Technol, Fac Biosci & Biotechnol, Yokohama, Kanagawa 2268501, Japan
[2] Nihon Univ, Sch Med, Dept Anat, Tokyo 1738601, Japan
[3] Tokyo Inst Technol, Frontier Collaborat Res Ctr, Yokohama, Kanagawa 2268503, Japan
[4] Mitsubishi Chem Corp, Inst Life Sci, Machida, Tokyo 1948511, Japan
[5] Univ Tokyo, Inst Med Sci, Tokyo 1088639, Japan
[6] Keio Univ, Fac Sci & Technol, Yokohama, Kanagawa 2238522, Japan
关键词
affinity purification; NF-kappa B; Ref-1; FK506-binding protein (FKBP); FK506; drug receptor identification;
D O I
10.1038/78496
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
We have developed a method using novel latex beads for rapid identification of drug receptors using affinity purification. Composed of a glycidylmethacrylate (GMA) and styrene copolymer core with a GMA polymer surface, the beads minimize nonspecific protein binding and maximize purification efficiency. We demonstrated their performance by efficiently purifying FK506-binding protein using FK506-conjugated beads, and found that the amount of material needed was significantly reduced compared with previous methods. Using the latex beads, we identified a redox-related factor, Ref-1, as a target protein of an anti-NF-kappa B drug, E3330, demonstrating the existence of a new class of receptors of anti-NF-kappa B drugs. Our results suggest that the latex beads could provide a tool for the identification and analysis of drug receptors and should therefore be useful in drug development.
引用
收藏
页码:877 / 881
页数:5
相关论文
共 19 条
[1]   SELECTIVE ENZYME PURIFICATION BY AFFINITY CHROMATOGRAPHY [J].
CUATRECA.P ;
WILCHEK, M ;
ANFINSEN, CB .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1968, 61 (02) :636-&
[2]   AFFINITY CHROMATOGRAPHY [J].
CUATRECASAS, P ;
ANFINSEN, CB .
ANNUAL REVIEW OF BIOCHEMISTRY, 1971, 40 :259-+
[3]   ACCURATE TRANSCRIPTION INITIATION BY RNA POLYMERASE-II IN A SOLUBLE EXTRACT FROM ISOLATED MAMMALIAN NUCLEI [J].
DIGNAM, JD ;
LEBOVITZ, RM ;
ROEDER, RG .
NUCLEIC ACIDS RESEARCH, 1983, 11 (05) :1475-1489
[4]   A RECEPTOR FOR THE IMMUNOSUPPRESSANT FK506 IS A CIS-TRANS PEPTIDYL-PROLYL ISOMERASE [J].
HARDING, MW ;
GALAT, A ;
UEHLING, DE ;
SCHREIBER, SL .
NATURE, 1989, 341 (6244) :758-760
[5]  
Hiramoto M, 1998, J IMMUNOL, V160, P810
[6]  
Hogan JC, 1996, NATURE, V384, P17
[7]   Nuclear transport of the major capsid protein is essential for adeno-associated virus capsid formation [J].
Hoque, M ;
Ishizu, K ;
Matsumoto, A ;
Han, S ;
Arisaka, F ;
Takayama, M ;
Suzuki, K ;
Kato, K ;
Kanda, T ;
Watanabe, H ;
Handa, H .
JOURNAL OF VIROLOGY, 1999, 73 (09) :7912-7915
[8]   DIRECT PURIFICATION OF MULTIPLE ATF/E4TF3 POLYPEPTIDES FROM HELA-CELL CRUDE NUCLEAR EXTRACTS USING DNA AFFINITY LATEX-PARTICLES [J].
INOMATA, Y ;
KAWAGUCHI, H ;
HIRAMOTO, M ;
WADA, T ;
HANDA, H .
ANALYTICAL BIOCHEMISTRY, 1992, 206 (01) :109-114
[9]   PREPARATION OF DNA-CARRYING AFFINITY LATEX AND PURIFICATION OF TRANSCRIPTION FACTORS WITH THE LATEX [J].
INOMATA, Y ;
WADA, T ;
HANDA, H ;
FUJIMOTO, K ;
KAWAGUCHI, H .
JOURNAL OF BIOMATERIALS SCIENCE-POLYMER EDITION, 1994, 5 (04) :293-302
[10]   BACULOVIRUS EXPRESSION VECTORS - THE REQUIREMENTS FOR HIGH-LEVEL EXPRESSION OF PROTEINS, INCLUDING GLYCOPROTEINS [J].
MATSUURA, Y ;
POSSEE, RD ;
OVERTON, HA ;
BISHOP, DHL .
JOURNAL OF GENERAL VIROLOGY, 1987, 68 :1233-1250