Synthetic Route to Human Relaxin‑2 via Iodine-Free Sequential Disulfide Bond Formation
journal contributionposted on 18.10.2016, 00:00 authored by Xu Yang, Vasily Gelfanov, Fa Liu, Richard DiMarchi
A new synthetic route to human relaxin-2 has been established through a sequential disulfide bond formation process in the absence of iodine. It is enabled by a combination of cysteine protection with penicillin G acylase-labile Phacm and a newly identified thiol activator bis(5-(2-methoxyethoxy)-2-pyrimidinyl disulfide. The long-standing challenges in relaxin B-chain assembly and its poor solubility have been solved by the insertion of two isoacyl dipeptide segments. The overall yield was 25% from the B chain and 5.8% from the B-chain starting resin.
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Relaxininsertionrelaxin B-chain assemblyiodineSynthetic Routeabsencesequential disulfide bond formation processthiolB chainpenicillin G acylase-labile PhacmcombinationsolubilityactivatorIodine-Free Sequential Disulfide Bond Formationrelaxin -2isoacyl dipeptide segmentsresincysteine protectionHumanchallenge