Trends Biotechnol. 2013 Jan;31(1):2-3. doi: 10.1016/j.tibtech.2012.10.003. Epub 2012 Nov 7.
Hemoglobin (Hb) is one of the most studied proteins. However, oxidative toxicity associated with free Hb in circulation and its contribution to inflammation and complications of transfusion have only recently become active areas of research. New insights into the protective mechanisms of haptoglobin (Hp), a plasma protein, and a timely resolution of the crystal structure of the Hb-Hp complex made it possible to definitively link the functional and structural interplay between the two proteins. Here, we summarize current knowledge of the interactions between Hb and Hp under oxidative stress conditions, and how Hb's own damaging radicals are harnessed by complex formation. Potential therapeutic benefits of using Hp for inactivation and clearance of free Hb under a number of clinical settings are considered.
血红蛋白(Hb)是研究最多的蛋白质之一。然而,循环中游离 Hb 相关的氧化毒性及其对炎症和输血并发症的影响,直到最近才成为研究的热点。对触珠蛋白(Hp)这种血浆蛋白的保护机制的新认识,以及 Hb-Hp 复合物晶体结构的及时解析,使得明确这两种蛋白之间的功能和结构相互作用成为可能。在这里,我们总结了在氧化应激条件下 Hb 和 Hp 之间相互作用的最新知识,以及 Hb 自身的破坏性自由基如何通过形成复合物来加以利用。考虑了在多种临床情况下使用 Hp 使游离 Hb 失活和清除的潜在治疗益处。