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零连接聚合血红蛋白OxyVita的结构与氧化还原行为:与天然脱细胞聚合血红蛋白的比较

Structural and redox behavior of OxyVita, a zero-linked polymeric hemoglobin: comparison with natural acellular polymeric hemoglobins.

作者信息

Harrington John P, Orlik Kseniya, Zito Samantha L, Wollocko Jacek, Wollocko Hanna

机构信息

State University of New York, New Paltz, New York 12561, USA.

出版信息

Artif Cells Blood Substit Immobil Biotechnol. 2010 Apr;38(2):64-8. doi: 10.3109/10731191003634562.

Abstract

A zero-linked polymeric hemoglobin (OxyVita Hb) has been developed for application as an acellular therapeutic hemoglobin-based-oxygen-carrier (HBOC). For effective and safe oxygen binding, transport and delivery, an HBOC must meet essential molecular requirements related to its structural integrity and redox stability. OxyVita is a super polymer possessing an average M.wt. of 17 x 10(6) Da. Structural integrity was determined by unfolding studies of OxyVita in the presence of increasing concentrations of urea. The unfolding midpoints (D(1/2)) of different preparations of OxyVita (solution and powder forms) were compared to Lumbricus Hb (LtHb) and Arenicola Hb (ArHb), natural acellular polymeric hemoglobins, which are serving as models for an effective and safe acellular HBOC. Reduction studies of OxyVita Hb using endogenous reducing agents were also investigated. Results from these studies indicate that: 1) OxyVita Hb exhibits greater resistance to conformational change than either LtHb or ArHb in the reduced (oxyHb) state; and 2) the reduction of met OxyVita Hb to oxyHb occurs slowly in the presence of either ascorbic acid (70% reduction in 560 min.) or beta-NADH (40% reduction in 90 min.). These studies provide consistent evidence that OxyVita Hb possesses physiochemical properties that exhibit structural integrity and redox behavior necessary for functioning as an effective and safe HBOC within clinical applications. These results are in agreement with observations made by other investigators as to the reduction in heme-loss of OxyVita Hb, essential for the reversible binding/release of molecular oxygen within the circulatory system.

摘要

一种零连接的聚合血红蛋白(OxyVita Hb)已被开发用作一种基于无细胞治疗性血红蛋白的氧载体(HBOC)。为了实现有效且安全的氧结合、运输和递送,一种HBOC必须满足与其结构完整性和氧化还原稳定性相关的基本分子要求。OxyVita是一种平均分子量为17×10⁶ Da的超级聚合物。通过在浓度不断增加的尿素存在下对OxyVita进行展开研究来确定其结构完整性。将不同制剂形式(溶液和粉末形式)的OxyVita的展开中点(D₁/₂)与蚯蚓血红蛋白(LtHb)和沙蠋血红蛋白(ArHb)这两种天然无细胞聚合血红蛋白进行比较,它们被用作有效且安全的无细胞HBOC的模型。还研究了使用内源性还原剂对OxyVita Hb的还原情况。这些研究结果表明:1)在还原(氧合血红蛋白)状态下,OxyVita Hb比LtHb或ArHb表现出对构象变化更强的抗性;2)在抗坏血酸(560分钟内70%还原)或β - NADH(90分钟内40%还原)存在的情况下,高铁OxyVita Hb向氧合血红蛋白的还原过程缓慢。这些研究提供了一致的证据,表明OxyVita Hb具有作为临床应用中有效且安全的HBOC发挥功能所必需的结构完整性和氧化还原行为的物理化学性质。这些结果与其他研究者关于OxyVita Hb血红素损失减少的观察结果一致,这对于循环系统中分子氧的可逆结合/释放至关重要。

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