Chakrabartty Avi
Department of Medical Biophysics, University of Toronto, Toronto, ON M5G 2M9, Canada.
Proteotoxicity Solutions, Toronto, ON L4K 2E1, Canada.
Pharmaceuticals (Basel). 2024 Sep 17;17(9):1225. doi: 10.3390/ph17091225.
The disease of transthyretin (TTR) amyloidosis (ATTR) has been known since the 1960s, and during the past 60 or so years, there has been a sustained period of steady discoveries that have led to the current model of ATTR pathogenesis. More recent research has achieved major advances in both diagnostics and therapeutics for ATTR, which are having a significant impact on ATTR patients today. Aiding these recent achievements has been the remarkable ability of cryo-electron microscopy (EM) to determine high-resolution structures of amyloid fibrils obtained from individual patients. Here, we will examine the cryo-EM structures of transthyretin amyloid fibrils to explore the structural basis of the two monoclonal antibody therapies for ATTR that are in clinical trials, ALXN-2220 and Coramitug, as well as to point out potential applications of this approach to other systemic amyloid diseases.
转甲状腺素蛋白(TTR)淀粉样变性病(ATTR)自20世纪60年代就已为人所知,在过去约60年里,一直有持续不断的稳定发现,形成了目前ATTR发病机制的模型。最近的研究在ATTR的诊断和治疗方面都取得了重大进展,对如今的ATTR患者产生了重大影响。冷冻电子显微镜(EM)能够确定从个体患者获得的淀粉样纤维的高分辨率结构,这一非凡能力推动了这些最新成果的取得。在此,我们将研究转甲状腺素蛋白淀粉样纤维的冷冻电镜结构,以探索两种正在进行临床试验的用于ATTR的单克隆抗体疗法(ALXN - 2220和Coramitug)的结构基础,并指出这种方法在其他全身性淀粉样疾病中的潜在应用。