Journal of Virology · 1984 · 82 citations · 42 references
Life SciencesInfectious DiseasesMolecular BiologyMolecular VirologyMonoclonal AntibodiesVirologyAntibody CharacterizationAntibody-antigen RecognitionViral InfectionsViral MutationAntibody-mediated Viral NeutralizationAntibody-mediated Virus NeutralizationAntigenic Variation In VirusesMonoclonal Antibody RecognitionMutant IdentificationPhysical Genome MappingStructural Basis Of AntigenicityViral Glycoprotein Processing
A pseudorabies virus variant ( mar197 -1) containing a mutation in a viral glycoprotein with a molecular weight of 50,000 ( gp50 ) was isolated by selecting for resistance to a neurtralizing monoclonal antibody ( MCA50 -1) directed against gp50 . This mutant was completely resistant to neutralization with MCA50 -1 in the presence or absence of complement, and was therefore defined as a mar (monoclonal-antibody-resistant) mutant. The mutation did not affect neutralization with polyvalent immune serum. The mar197 -1 mutant synthesized and processed gp50 normally, but the mutation prevented the binding and immunoprecipitation of gp50 by MCA50 -1. Thus, the mutation was within the structural portion of the gp50 gene affecting the epitope of the monoclonal antibody. The mutation was mapped by marker rescue with cloned pseudorabies restriction enzyme fragments to the short region of the pseudorabies genome between 0.813 and 0.832 map units. This is equivalent to a 2.1-kilobase-pair region.
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Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4
Ulrich K. Laemmli · Nature · 1970 · 251.6K citations
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