Antibodies specific for (6-4) DNA photoproducts: cloning, antibody modeling and construction of a single-chain Fv derivative

被引:21
作者
Morioka, H
Miura, H
Kobayashi, H
Koizumi, T
Fujii, K
Asano, K
Matsunaga, T
Nikaido, O
Stewart, JD [1 ]
Ohtsuka, E
机构
[1] Univ Florida, Dept Chem, Gainesville, FL 32611 USA
[2] Kanazawa Univ, Fac Pharmaceut Sci, Kanazawa, Ishikawa 920, Japan
[3] Hokkaido Univ, Fac Pharmaceut Sci, Sapporo, Hokkaido 060, Japan
来源
BIOCHIMICA ET BIOPHYSICA ACTA-PROTEIN STRUCTURE AND MOLECULAR ENZYMOLOGY | 1998年 / 1385卷 / 01期
基金
美国国家科学基金会;
关键词
molecular recognition; photodamaged DNA; anti-nucleic acid antibody; single-chain Fv antibody fragment; computer modeling;
D O I
10.1016/S0167-4838(98)00029-6
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
We have investigated a series of four monoclonal antibodies that specifically recognize pyrimidine (6-4) pyrimidone photoproducts. One of these antibodies (64M4), bound all four possible pyrimidine-pyrimidone photoadducts with equal affinities whereas the others (64M2, 64M3 and 64M5) were selective for TC and TT sequences. In addition, 64M5 had the highest binding affinity for photodamaged DNA of the four [T. Mori et al., Photochem. Photobiol. 54 (1991) 225-232]. To help understand the differences between these antibodies, we have cloned and sequenced the variable region genes from all four. Comparing these sequences revealed that all four were highly similar to one another, although there were some differences in potential antigen-contact regions. To assess the influences of these sequence differences at the structural level, computer models were constructed for all four antibodies. Most of the sequence differences occurred in potential antigen contact regions, suggesting specific positions that might account for the observed differences in binding affinities and selectivities. A single-chain Fv derivative of 64M5 was therefore constructed and characterized to provide an experimental system in which structure-function relationships can be tested. This derivative could be isolated from Escherichia coli using two chromatographic steps and possessed the same binding specificity as the parent monoclonal antibody. (C) 1998 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:17 / 32
页数:16
相关论文
共 69 条
[61]   A NEW PHOTOREACTIVATING ENZYME THAT SPECIFICALLY REPAIRS ULTRAVIOLET LIGHT-INDUCED (6-4)PHOTOPRODUCTS [J].
TODO, T ;
TAKEMORI, H ;
RYO, H ;
IHARA, M ;
MATSUNAGA, T ;
NIKAIDO, O ;
SATO, K ;
NOMURA, T .
NATURE, 1993, 361 (6410) :371-374
[62]   AN ULTRAVIOLET LIGHT-DAMAGED DNA RECOGNITION PROTEIN ABSENT IN XERODERMA-PIGMENTOSUM GROUP-E CELLS BINDS SELECTIVELY TO PYRIMIDINE (6-4) PYRIMIDONE PHOTOPRODUCTS [J].
TREIBER, DK ;
CHEN, ZH ;
ESSIGMANN, JM .
NUCLEIC ACIDS RESEARCH, 1992, 20 (21) :5805-5810
[63]   REFINED CRYSTAL-STRUCTURE OF THE INFLUENZA VIRUS-N9 NEURAMINIDASE NC41 FAB COMPLEX [J].
TULIP, WR ;
VARGHESE, JN ;
LAVER, WG ;
WEBSTER, RG ;
COLMAN, PM .
JOURNAL OF MOLECULAR BIOLOGY, 1992, 227 (01) :122-148
[64]   ATOMIC MODEL OF A PYRIMIDINE DIMER EXCISION-REPAIR ENZYME COMPLEXED WITH A DNA SUBSTRATE - STRUCTURAL BASIS FOR DAMAGED DNA RECOGNITION [J].
VASSYLYEV, DG ;
KASHIWAGI, T ;
MIKAMI, Y ;
ARIYOSHI, M ;
IWAI, S ;
OHTSUKA, E ;
MORIKAWA, K .
CELL, 1995, 83 (05) :773-782
[65]  
VONHIPPEL PH, 1986, LIGAND INTERACTIONS, V137, P159
[66]   ANTIBODIES TO UV IRRADIATED DNA - THE MONITORING OF DNA DAMAGE BY ELISA AND INDIRECT IMMUNOFLUORESCENCE [J].
WANI, AA ;
GIBSONDAMBROSIO, RE ;
DAMBROSIO, SM .
PHOTOCHEMISTRY AND PHOTOBIOLOGY, 1984, 40 (04) :465-471
[67]  
WHITLOW M, 1991, Methods (Orlando), V2, P97, DOI 10.1016/S1046-2023(05)80209-9
[68]   DNA repair in eukaryotes [J].
Wood, RD .
ANNUAL REVIEW OF BIOCHEMISTRY, 1996, 65 :135-167
[69]   A EUKARYOTIC GENE ENCODING AN ENDONUCLEASE THAT SPECIFICALLY REPAIRS DNA DAMAGED BY ULTRAVIOLET-LIGHT [J].
YAJIMA, H ;
TAKAO, M ;
YASUHIRA, S ;
ZHAO, JH ;
ISHII, C ;
INOUE, H ;
YASUI, A .
EMBO JOURNAL, 1995, 14 (10) :2393-2399