1979
DOI: 10.1016/0041-008x(79)90006-1
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Chemical characterization of isocyanate-protein conjugates

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1983
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Cited by 66 publications
(28 citation statements)
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“…The investigated workers neither exhibited asthmatic symptoms nor the aberrant serotonin kinetic characteristics for endogenous asthma. Organic isocyanates react in vitro with free amino groups and other sites in proteins (6,28). Hexarnethylenediisocyanate was present in the hardeners used by our workers.…”
Section: Discussionmentioning
confidence: 94%
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“…The investigated workers neither exhibited asthmatic symptoms nor the aberrant serotonin kinetic characteristics for endogenous asthma. Organic isocyanates react in vitro with free amino groups and other sites in proteins (6,28). Hexarnethylenediisocyanate was present in the hardeners used by our workers.…”
Section: Discussionmentioning
confidence: 94%
“…The isocyanates react in vitro with free amino groups and other sites on protein molecules. The reaction products may be sirnilar to derivatives formed in vivo which cause immunogenic and/or allergenic symptoms in exposed workers (28). With hydrolysis hexamethylene diisocyanate, which was present in low amounts in the hardeners used by the workers in the present study, yields hexarnethylenediamine, a toxic substance, the fumes of which have been shown to cause respiratory difficulties in exposed rats (6).…”
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confidence: 93%
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“…10 Isocyanates react rapidly with proteins in vitro and in vivo, and isocyanate-protein conjugates are believed to represent the major immunogenic form of the chemical. 6,9,11,12 In exposed humans, albumin in the airway fluid is a major target for isocyanate and isocyanate-albumin conjugates are the only known "isocyanate antigen" specifically recognized by rearranged antigen receptors of the adaptive immune system (i.e. IgG).…”
Section: Introductionmentioning
confidence: 99%
“…Lysine was our first choice, as in vitro studies had shown that, when added to proteins, isocyanates and anhydrides react with this amino acid (52,53). Lysine has an epsilon amino group which can take part in the reaction and has also been shown to be the most likely residue for the covalent binding of chloramine-T to a protein, although tyrosine, methionine, cysteine, and histidine were also modified by the substance (54).…”
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confidence: 99%