Identification of scFv antibody fragments that specifically recognise the heroin metabolite 6-monoacetylmorphine but not morphine

被引:48
作者
Moghaddam, A
Borgen, T
Stacy, J
Kausmally, L
Simonsen, B
Marvik, OJ
Brekke, OH
Braunagel, M
机构
[1] Affitech AS, N-0349 Oslo, Norway
[2] GeNova AS, N-0349 Oslo, Norway
关键词
scFv; antibody fragments; 6-monoacetylmorphine;
D O I
10.1016/S0022-1759(03)00109-1
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Use of phage display of recombinant antibodies and large repertoire naive antibody libraries for identifying antibodies of high specificity has been extensively reported. Nevertheless, there have been few reported antibodies to haptens that have originated from naive antibody libraries with potential use in diagnostics. We have used chain shuffling of lead single-chain fragment variable (scFv) antibodies, isolated from a naive antibody library, to screen for antibodies that specifically recognise the major metabolite of heroin, 6-monoacetylmorphine (6MAM). The antibodies were identified by screening high-density colonies of Escherichia coli expressing soluble scFv antibody fragments without prior expression on bacteriophage (phage display). The antibodies recognise 6MAM with affinities of 1-3 x 10(-7) M with no crossreactivity to morphine. These antibodies can potentially be used for developing a rapid immunoassay in drug-testing programs. To our knowledge, this is the first report of an antibody that distinguishes 6MAM from its de-acetylated form, morphine. (C) 2003 Elsevier B.V. All rights reserved.
引用
收藏
页码:139 / 155
页数:17
相关论文
共 55 条
[1]   Construction of a semisynthetic antibody library using trinucleotide oligos [J].
Braunagel, M ;
Little, M .
NUCLEIC ACIDS RESEARCH, 1997, 25 (22) :4690-4691
[2]   Improving antibody affinity by mimicking somatic hypermutation in vitro [J].
Chowdhury, PS ;
Pastan, I .
NATURE BIOTECHNOLOGY, 1999, 17 (06) :568-572
[3]   Isolation of a high-affinity stable single-chain Fv specific for mesothelin from DNA-immunized mice by phage display and construction of a recombinant immunotoxin with anti-tumor activity [J].
Chowdhury, PS ;
Viner, JL ;
Beers, R ;
Pastan, I .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (02) :669-674
[4]   MAKING ANTIBODY FRAGMENTS USING PHAGE DISPLAY LIBRARIES [J].
CLACKSON, T ;
HOOGENBOOM, HR ;
GRIFFITHS, AD ;
WINTER, G .
NATURE, 1991, 352 (6336) :624-628
[5]   Streptabody, a high avidity molecule made by tetramerization of in vivo biotinylated, phage display-selected scFv fragments on streptavidin [J].
Cloutier, SM ;
Couty, S ;
Terskikh, A ;
Marguerat, L ;
Crivelli, V ;
Pugnières, M ;
Mani, JC ;
Leisinger, HJ ;
Mach, JP ;
Deperthes, D .
MOLECULAR IMMUNOLOGY, 2000, 37 (17) :1067-1077
[6]   A BINARY PLASMID SYSTEM FOR SHUFFLING COMBINATORIAL ANTIBODY LIBRARIES [J].
COLLET, TA ;
ROBEN, P ;
OKENNEDY, R ;
BARBAS, CF ;
BURTON, DR ;
LERNER, RA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (21) :10026-10030
[7]   Functional characterization of an anti-estradiol antibody by site-directed mutagenesis and molecular modelling:: modulation of binding properties and prominent role of the VL domain in estradiol recognition [J].
Coulon, S ;
Pellequer, JL ;
Blachère, T ;
Chartier, M ;
Mappus, E ;
Chen, SWW ;
Cuilleron, CY ;
Baty, D .
JOURNAL OF MOLECULAR RECOGNITION, 2002, 15 (01) :6-18
[8]   Construction and evolution of antibody-phage libraries by DNA shuffling [J].
Crameri, A ;
Cwirla, S ;
Stemmer, WPC .
NATURE MEDICINE, 1996, 2 (01) :100-102
[9]   Creating and engineering human antibodies for immunotherapy [J].
de Haard, H ;
Henderikx, P ;
Hoogenboom, HR .
ADVANCED DRUG DELIVERY REVIEWS, 1998, 31 (1-2) :5-31
[10]   A large non-immunized human Fab fragment phage library that permits rapid isolation and kinetic analysis of high affinity antibodies [J].
de Haard, HJ ;
van Neer, N ;
Reurs, A ;
Hufton, SE ;
Roovers, RC ;
Henderikx, P ;
de Bruïne, AP ;
Arends, JW ;
Hoogenboom, HR .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (26) :18218-18230