HOMOLOGIES BETWEEN GRAIN STORAGE PROTEINS OF DIFFERENT CEREAL SPECIES .2. EFFECTS OF ASSAY FORMAT AND GRAIN EXTRACTANT ON ANTIBODY CROSS-REACTIVITY

被引:10
作者
SKERRITT, JH
HILL, AS
机构
[1] CSIRO Wheat Research Unit, Division of Plant Industry, North Ryde, New South Wales, 2113
关键词
2,2´-azinobis-3-ethylbenzthiazoline sulfonic acid; 5-bromo-4-chloro-3-indolyl phosphate; ABTS; BCIP; bovine serum albumin; BSA; chloroform/methanol-soluble; CM; dimethyl formamide; DMF; EIA; ELISA; enzyme immunoassay; enzyme-linked immunosorbent assay; high molecular weight; HMW; horseradish peroxidase; HRP; LMW; low molecular weight; ME; mercaptoethanol; NBT; NC; nitroblue tetrazolium; nitrocellulose; polyacrylamide gel electrophoresis in the presence of sodium dodecyl sulfate; polyvinylchloride; PVC; SDS-PAGE; TBST; Tris-buffered saline-Tween 20;
D O I
10.1016/S0733-5210(09)80115-X
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
A variety of monoclonal antibodies with specificities for different wheat grain storage proteins has been shown to exhibit a number of differing cross-reaction patterns with grain storage proteins from related cereal species (Skerritt and Lew, J. Cereal Sci. 11 (1990) 103-121). This antibody library provides an opportunity to measure the effects of a range of immunoassay methodological variables on the cross-reactivity of these antibodies. Variation of the extractant used for grain proteins from different cereals altered both the amount and composition of protein extracted and thus the cross-reaction of the antibodies. Antibody cross-reactivity was greater when nitrocellulose membrane solid phases compared with polystyrene microwells were used for indirect enzyme linked immunosorbent assay (ELISA). Quite differing cross-reactivity results were obtained when the same grain protein extracts were used in indirect, antigen-competition and sandwich-type assay formats. In the sandwich assay format, alteration of either the solid phase-bound or labelled antibody altered apparent antibody specificity. These results indicate that it is important when reporting immunological homology data, to define cross-reaction of antibodies with respect to the assay format used. Antibody specificity (or cross-reactivity) can be manipulated by variation of sample extractant, solid phase and the format of the assay. © 1990, Academic Press Limited. All rights reserved.
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收藏
页码:123 / 141
页数:19
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