Bioconjugation via Hetero-Selective Clamping of Two Different Amines with ortho-Phthalaldehyde

Amino groups are common in both natural and synthetic compounds and offer a very attractive class of endogenous handles for bioconjugation. However, the ability to differentiate two types of amino groups and join them with high hetero-selectivity and efficiency in a complex setting remains elusive. Herein, we report a new method for bioconjugation via one-pot chemoselective clamping of two different amine nucleophiles using a simple ortho-phthalaldehyde (OPA) reagent. Various alpha-amino acids, aryl amines, and secondary amines can be crosslinked to the epsilon-amino side chain of lysine on peptides or proteins with high efficiency and hetero-selectivity. This method offers a simple and powerful means to crosslink small molecule drugs, imaging probes, peptides, proteins, carbohydrates, and even virus particles without any pre-functionalization.

Automated summary

In this study, a simple and powerful method for bioconjugation is reported, using ortho-phthalaldehyde (OPA) reagent to efficiently and selectively crosslink various alpha-amino acids, aryl amines, and secondary amines to the epsilon-amino side chain of lysine on peptides or proteins.