Literature DB >> 2764726

Spurious cross-reactions between plant viruses and monoclonal antibodies can be overcome by saturating ELISA plates with milk proteins.

D Zimmermann1, M H Van Regenmortel.   

Abstract

It has been claimed recently [Dietzgen (1986) Arch Virol 91: 163-173] that a series of monoclonal antibodies (Mabs) produced against the nepovirus, arabis mosaic virus (ArMV) cross-reacted with the tobamovirus, tobacco mosaic virus (TMV). In the present report, this alleged cross-reactivity was re-examined by two ELISA procedures using Mabs produced against each of the two viruses. It was found that when highly concentrated preparations of Mabs were used, all antibodies reacted in a nonspecific manner with several plant viruses. However, when defatted milk instead of bovine serum albumin was used both as blocking agent and as diluent for the Mabs, the spurious cross-reactions between unrelated viruses were abolished. The use of milk as blocking agent did not prevent the detection of genuine cross-reactions between related nepoviruses.

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Year:  1989        PMID: 2764726     DOI: 10.1007/BF01311034

Source DB:  PubMed          Journal:  Arch Virol        ISSN: 0304-8608            Impact factor:   2.574


  13 in total

1.  Visualization by electron microscopy of the location of tobacco mosaic virus epitopes reacting with monoclonal antibodies in enzyme immunoassay.

Authors:  I Dore; E Weiss; D Altschuh; M H Van Regenmortel
Journal:  Virology       Date:  1988-02       Impact factor: 3.616

2.  Quantitative differences among various proteins as blocking agents for ELISA microtiter plates.

Authors:  R F Vogt; D L Phillips; L O Henderson; W Whitfield; F W Spierto
Journal:  J Immunol Methods       Date:  1987-07-16       Impact factor: 2.303

3.  Antigenicity of histones: comparative studies on histones with very high lysine content from various sources.

Authors:  M Sluyser; P Rümke; A Hekman
Journal:  Immunochemistry       Date:  1969-05

4.  Immunological properties and biological function of monoclonal antibodies to tobacco mosaic virus.

Authors:  R G Dietzgen
Journal:  Arch Virol       Date:  1986       Impact factor: 2.574

5.  Separation of anti-histone antibodies from nonimmune histone-precipitating serum proteins, predominantly alpha2-macroglobulin.

Authors:  B D Stollar; W Rezuke
Journal:  Arch Biochem Biophys       Date:  1978-10       Impact factor: 4.013

6.  Immunochemical cross-reactivity between the dissociated capsid proteins of PVY group plant viruses.

Authors:  J F Shepard; G A Secor; D E Purcifull
Journal:  Virology       Date:  1974-04       Impact factor: 3.616

7.  Detection of a wide spectrum of tobacco mosaic virus strains by indirect enzyme-linked immunosorbent assays (ELISA).

Authors:  M H Van Regenmortel; J Burckard
Journal:  Virology       Date:  1980-10-30       Impact factor: 3.616

8.  Characterization of antigenic structures on arabis mosaic virus with monoclonal antibodies.

Authors:  R G Dietzgen
Journal:  Arch Virol       Date:  1986       Impact factor: 2.574

9.  A major part of the polypeptide chain of tobacco mosaic virus protein is antigenic.

Authors:  Z A Moudallal; J P Briand; M H Regenmortel
Journal:  EMBO J       Date:  1985-05       Impact factor: 11.598

10.  Monoclonal antibodies as probes of the antigenic structure of tobacco mosaic virus.

Authors:  Z Al Moudallal; J P Briand; M H Van Regenmortel
Journal:  EMBO J       Date:  1982       Impact factor: 11.598

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  2 in total

Review 1.  Protein antigenicity.

Authors:  M H Van Regenmortel
Journal:  Mol Biol Rep       Date:  1992-06       Impact factor: 2.316

2.  Genome analysis and detection of a Chilean isolate of Grapevine leafroll associated virus-3.

Authors:  Esteban A Engel; Cristobal Girardi; Paula F Escobar; Vania Arredondo; Calixto Domínguez; Tomás Pérez-Acle; Pablo D T Valenzuela
Journal:  Virus Genes       Date:  2008-05-23       Impact factor: 2.332

  2 in total

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