Preparation of protein conjugates via intermolecular disulfide bond formation

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Abstract
Conjugates of 2 unlike proteins can be prepared via the intermolecular disulfide interchange reaction, i.e., protein A containing thiol groups reacts with protein B containing 4-dithiopyridyl groups to yield a conjugate with the release of 4-thiopyridone. Thiol groups can be introduced into proteins on amidination with methyl 3-mercaptopropionimidate ester or 2-iminothiolane, and 4-dithiopyridyl groups can be introduced into proteins with these same reagents in the presence of 4,4''-dithiodipyridine. 2-Iminothiolane is stable on storage in contrast to the known lability of imidate esters; therefore 2-iminothiolane is a more convenient reagent for the modification of proteins than are the imidate esters. All the reactions can be carried out easily under mild conditions in good yields. Conjugates of bovine plasma albumin with itself, RNase or a copolymer of D-glutamic acid and D-lysine and of sheep antibody and horseradish peroxidase were prepared with modified proteins containing an average of 1-5 thiol or dithiopyridyl groups per mol. These conjugates formed mainly dimers, trimers and tetramers. The peroxidase labeled antibody retained more than 80% of its enzymatic and antigenic binding activities.