Sites of Modification of Hemospan, a Poly(ethylene glycol)-Modified Human Hemoglobin for Use As an Oxygen Therapeutic

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• 作者：Kim D. Vandegriff ; Ashok Malavalli ; Gnel M. Mkrtchyan ; Stephanie N. Spann ; Dale A. Baker ; Robert M. Winslow
• 刊名：Bioconjugate Chemistry
• 出版年：2008
• 出版时间：November 19, 2008
• 年：2008
• 卷：19
• 期：11
• 页码：2163-2170
• 全文大小：367K
• 年卷期：v.19,no.11(November 19, 2008)
• ISSN：1520-4812

文摘

Hemospan is an acellular hemoglobin-based oxygen therapeutic in clinical trials in Europe and the United States. The product is prepared by site-specific conjugation of maleimide-activated poly(ethylene) glycol (PEG, MW 5500) to human oxyhemoglobin through maleimidation reactions either (1) directly to reactive Cys thiols or (2) at surface Lys groups following thiolation using 2-iminothiolane. The thiolation/maleimidation reactions lead to the addition of 8 PEGs per hemoglobin tetramer. Identification of PEG modified globins by SDS-PAGE and MALDI-TOF reveals a small percentage of protein migrating at the position for unmodified globin chains and the remaining as separate bands representing globin chains conjugated with 1 to 4 PEGs per chain. Identification of PEG modification sites on individual α and β globins was made using reverse-phase HPLC, showing a series of α globins conjugated with 0 to 3 PEGs and a series of β globins conjugated with 0 to 4 PEGs per globin. Mass analysis of tryptic peptides from hemoglobin thiolated and maleimidated with N-ethyl maleimide showed the same potential sites of modification regardless of thiolation reaction ratio, with seven sites identified on β globins at β8, β17, β59, β66, β93, β95, and β132 and three sites identified on α globins at α7, α16, and α40.