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Merck

High efficiency reduction capability for the formation of Fab׳ antibody fragments from F(ab)

Biochemistry and biophysics reports (2015-04-25)
Victor Crivianu-Gaita, Alexander Romaschin, Michael Thompson
RESUMO

Antibodies have widespread applications in areas ranging from therapeutics to chromatography and protein microarrays. Certain applications require only the fragment antigen-binding (Fab) units of the protein. This study compares the cleavage efficacy of dithiothreitol (DTT), mercaptoethylamine (MEA), and dithiobutylamine (DTBA) - a relatively new reducing agent synthesized in 2012. Pseudo-first order kinetic analyses show DTBA to be ~213 times faster than DTT and ~71 times faster than MEA in the formation of Fab׳ antibody fragments from polyclonal rabbit antibodies. Monoclonal mouse antibodies were also used to show the feasibility of the reduction process on antibodies from a different species and with a different clonality. DTBA cleaved the monoclonal mouse F(ab)

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Sigma-Aldrich
Monoclonal Anti-Human IgG1 antibody produced in mouse, clone 8c/6-39, ascites fluid
Sigma-Aldrich
Anti-Goat IgG (whole molecule) antibody produced in rabbit, IgG fraction of antiserum, buffered aqueous solution