Amplified detection, using a monoclonal antibody, of an aphid-specific epitope exposed during digestion in the gut of a predator

被引:27
作者
Symondson, WOC [1 ]
Erickson, ML [1 ]
Liddell, JE [1 ]
Jayawardena, KGI [1 ]
机构
[1] Cardiff Univ, Cardiff Sch Biosci, Cardiff CF1 3TL, S Glam, Wales
基金
英国生物技术与生命科学研究理事会;
关键词
cereal aphids; Pterostichus melanarius; monoclonal antibody; epitope; detection period; digestion; trophic interactions;
D O I
10.1016/S0965-1748(99)00063-6
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
Monoclonal antibodies are invaluable tools for identifying and quantifying prey remains in the fore-guts of predators. However, they must be target-specific, detect an epitope that is well replicated within the prey (to enhance assay sensitivity) and, critically, recognise a site that can resist digestion. A monoclonal antibody is reported that proved to be aphid-specific and capable of detecting. and accurately identifying, as little as 16.5 ng of aphid protein within a heterologous mixture of invertebrate material. The antibody was selected by screening hybridoma lines for antibodies that bound with semi-digested aphid proteins. The antibody detected an epitope that was found, against expectation, to significantly increase in concentration with time (by approx. 50% over 6 h) in the gut of the carabid predator Pterostichus melanarius. The resultant extended antigen detection period and half-life, and the high specificity of this antibody, showed it to be an enhanced tool for studying interactions between aphids and their predators in the field. It was concluded that the antibody was initially generated to a surface epitope on a high molecular weight native protein (>200 kD). This epitope, however, was then either replicated on internal sites progressively revealed by digestion, or new epitopes became available as the conformation of the protein changed during digestion. (C) 1999 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:873 / 882
页数:10
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