Site-Specific PEGylation at Histidine Tags

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• 作者：Yuehua Cong ; Estera Pawlisz ; Penny Bryant ; Sibu Balan ; Emmanuelle Laurine ; Rita Tommasi ; Ruchi Singh ; Sitara Dubey ; Karolina Peciak ; Matthew Bird ; Amrita Sivasankar ; Julia Swierkosz ; Maurizio Muroni ; Sibylle Heidelberger ; Monika Farys ; Farzad Khayrzad ; Jeff Edwards ; George Badescu ; Ian Hodgson ; Charles Heise ; Satyanarayana Somavarapu ; John Liddell ; Keith Powell ; Mire Zloh ; Ji-won Choi ; Antony Godwin ; Steve Brocchini
• 刊名：Bioconjugate Chemistry
• 出版年：2012
• 出版时间：February 15, 2012
• 年：2012
• 卷：23
• 期：2
• 页码：248-263
• 全文大小：658K
• 年卷期：v.23,no.2(February 15, 2012)
• ISSN：1520-4812

文摘

The efficacy of protein-based medicines can be compromised by their rapid clearance from the blood circulatory system. Achieving optimal pharmacokinetics is a key requirement for the successful development of safe protein-based medicines. Protein PEGylation is a clinically proven strategy to increase the circulation half-life of protein-based medicines. One limitation of PEGylation is that there are few strategies that achieve site-specific conjugation of PEG to the protein. Here, we describe the covalent conjugation of PEG site-specifically to a polyhistidine tag (His-tag) on a protein. His-tag site-specific PEGylation was achieved with a domain antibody (dAb) that had a 6-histidine His-tag on the C-terminus (dAb-His₆) and interferon 伪-2a (IFN) that had an 8-histidine His-tag on the N-terminus (His₈-IFN). The site of PEGylation at the His-tag for both dAb-His₆-PEG and PEG-His₈-IFN was confirmed by digestion, chromatographic, and mass-spectral studies. A methionine was also inserted directly after the N-terminal His-tag in IFN to give His₈Met-IFN. Cyanogen bromide digestion studies of PEG-His₈Met-IFN were also consistent with PEGylation at the His-tag. By using increased stoichiometries of the PEGylation reagent, it was possible to conjugate two separate PEG molecules to the His-tag of both the dAb and IFN proteins. Stability studies followed by in vitro evaluation confirmed that these PEGylated proteins retained their biological activity. In vivo PK studies showed that all of the His-tag PEGylated samples displayed extended circulation half-lives. Together, our results indicate that site-specific, covalent PEG conjugation at a His-tag can be achieved and biological activity maintained with therapeutically relevant proteins.