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pubmed-article:1378474pubmed:abstractTextThe interactions of two monoclonal antibodies with human growth hormone (hGH) have been investigated. The individual antibodies showed normal behavior in a competitive binding assay, but mixtures of the antibodies demonstrated a 'hook' attributable to cooperative interactions. Cooperativity was observed in titrations which preceded the competitive binding assay. Size exclusion chromatographic data suggest that the cooperativity is explained by the formation of higher molecular weight complexes (up to 700 kDa). The major complex is probably linear, consisting of three antibody molecules. Circular and linear complexes with four antibody molecules (octameric complexes) are also possible. Theoretical models also support the formation of cyclic complexes in a competitive binding assay.lld:pubmed
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pubmed-article:1378474pubmed:authorpubmed-author:WilsonG SGSlld:pubmed
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pubmed-article:1378474pubmed:pagination27-46lld:pubmed
pubmed-article:1378474pubmed:dateRevised2007-11-14lld:pubmed
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pubmed-article:1378474pubmed:year1992lld:pubmed
pubmed-article:1378474pubmed:articleTitleStudies of the low dose 'hook' effect in a competitive homogeneous immunoassay.lld:pubmed
pubmed-article:1378474pubmed:affiliationDepartment of Chemistry, University of Kansas, Lawrence 66045.lld:pubmed
pubmed-article:1378474pubmed:publicationTypeJournal Articlelld:pubmed
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pubmed-article:1378474pubmed:publicationTypeResearch Support, U.S. Gov't, P.H.S.lld:pubmed