Department of General Biochemistry, Faculty of Biology and Environmental Protection, University of Lodz, Pomorska 141/143, 90-236 Lodz, Poland.
Int J Mol Sci. 2021 Dec 13;22(24):13370. doi: 10.3390/ijms222413370.
Kininogens are multidomain glycoproteins found in the blood of most vertebrates. High molecular weight kininogen demonstrate both carrier and co-factor activity as part of the intrinsic pathway of coagulation, leading to thrombin generation. Kininogens are the source of the vasoactive nonapeptide bradykinin. To date, attempts to crystallize kininogen have failed, and very little is known about the shape of kininogen at an atomic level. New advancements in the field of cryo-electron microscopy (cryoEM) have enabled researchers to crack the structure of proteins that has been refractory to traditional crystallography techniques. High molecular weight kininogen is a good candidate for structural investigation by cryoEM. The goal of this review is to summarize the findings of kininogen structural studies.
激肽原是在大多数脊椎动物的血液中发现的多结构域糖蛋白。高分子量激肽原作为凝血固有途径的一部分,表现出载体和辅助因子活性,导致凝血酶生成。激肽原是血管活性九肽缓激肽的来源。迄今为止,结晶激肽原的尝试均以失败告终,而且人们对激肽原在原子水平上的形状知之甚少。冷冻电子显微镜(cryoEM)领域的新进展使研究人员能够破解传统晶体学技术难以解决的蛋白质结构。高分子量激肽原是 cryoEM 结构研究的良好候选者。本综述的目的是总结激肽原结构研究的结果。