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- Title
Development of an ELISA and Immunochromatographic Strip for Highly Sensitive Detection of Microcystin-LR.
- Authors
Liqiang Liu; Changrui Xing; Huijuan Yan; Hua Kuang; Chuanlai Xu
- Abstract
A monoclonal antibody for microcystin-leucine-arginine (MC-LR) was produced by cell fusion. The immunogen was synthesized in two steps. First, ovalbumin/ bovine serum albumin was conjugated with 6-acetylthiohexanoic acid using a carbodiimide EDC (1-ethyl-3-[3-dimethylaminopropyl]carbodiimide hydrochloride)/NHS (N-hydroxysulfosuccinimide) reaction. After dialysis, the protein was reacted with MC-LR based on a free radical reaction under basic solution conditions. The protein conjugate was used for immunization based on low volume. The antibodies were identified by indirect competitive (ic)ELISA and were subjected to tap water and lake water analysis. The concentration causing 50% inhibition of binding of MC-LR (IC50) by the competitive indirect ELISA was 0.27 ng/mL. Cross-reactivity to the MC-RR, MC-YR and MC-WR was good. The tap water and lake water matrices had no effect on the detection limit. The analytical recovery of MC-LR in the water samples in the icELISA was 94%-110%. Based on this antibody, an immunochromatographic biosensor was developed with a cut-off value of 1 ng/mL, which could satisfy the requirement of the World Health Organization for MC-LR detection in drinking water. This biosensor could be therefore be used as a fast screening tool in the field detection of MC-LR.
- Subjects
MONOCLONAL antibodies; IMMUNOGENETICS; OVALBUMINS; MICROCYSTINS; CARBODIIMIDES; BIOSENSOR research
- Publication
Sensors (14248220), 2014, Vol 14, Issue 8, p14672
- ISSN
1424-8220
- Publication type
Article
- DOI
10.3390/s140814672