Key result
~90% of monoclonal antibodies against cTnI target linear epitopes at the N- or C-terminal ends.
Why the study?
Generation and epitope mapping of monoclonal antibodies specific to human cardiac troponin I are needed to enable reliable detection of TnI in serum of patients with acute myocardial infarction.
The generation and epitope mapping of monoclonal antibodies recognizing both isolated cTnI and cTnI within the troponin complex supports reliable detection of TnI in patients with acute myocardial infarction.
May guide troponin immunoassay design; leaves open clinical translation from this animal study.
Two groups of monoclonal antibodies (MAbs) specific to human cardiac troponin I (cTnI) were generated by immunization of mice by isolated cTnI (group I, 16 MAbs) or by the whole troponin complex (group II, 15 MAbs). Two sets of overlapping decapeptides covering the complete sequence of cTnI were prepared and used for epitope mapping by SPOT technique. Majority of MAbs (28 out of 31) interacts with synthetic peptides thus indicating that they recognize liner epitopes. MAbs raised against isolated cTnI preferentially recognize epitopes located at the N- or C-terminal ends of cTnI. Nine out of fifteen MAbs raised against whole troponin complex interact with epitopes located in the N-terminal part of cTnI. Generation of MAbs recognizing both isolated cTnI and cTnI inside of troponin complex and mapping their epitopes provides reliable detection of TnI in serum of patients with acute myocardial infarction.
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Filatov et al. (1998) studied Acute myocardial infarction. Monoclonal antibodies specific to human cardiac troponin I was evaluated on Epitope mapping of monoclonal antibodies. The majority of monoclonal antibodies (28 out of 31) raised against isolated cTnI or the whole troponin complex recognized linear epitopes, primarily at the N- or C-terminal ends of cTnI.
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