Department of Biosciences, Università degli Studi di Milano, Milan, Italy. Electronic address: https://twitter.com/@Saritapuri1504.
Institute of Molecular and Translational Cardiology, IRCCS Policlinico San Donato, 20097 Milan, Italy. Electronic address: https://twitter.com/@timpaul81.
J Mol Biol. 2023 Sep 15;435(18):168215. doi: 10.1016/j.jmb.2023.168215. Epub 2023 Jul 27.
Immunoglobulin light chain amyloidosis (AL) is caused by the aberrant production of amyloidogenic light chains (LC) that accumulate as amyloid deposits in vital organs. Distinct LC sequences in each patient yield distinct amyloid structures. However different tissue microenvironments may also cause identical protein precursors to adopt distinct amyloid structures. To address the impact of the tissue environment on the structural polymorphism of amyloids, we extracted fibrils from the kidney of an AL patient (AL55) whose cardiac amyloid structure was previously determined by our group. Here we show that the 4.0 Å resolution cryo-EM structure of the renal fibril is virtually identical to that reported for the cardiac fibril. These results provide the first structural evidence that LC amyloids independently deposited in different organs of the same AL patient share a common fold.
免疫球蛋白轻链淀粉样变性 (AL) 是由异常产生的淀粉样轻链 (LC) 引起的,这些 LC 在重要器官中积累形成淀粉样沉积物。每位患者的独特 LC 序列产生独特的淀粉样结构。然而,不同的组织微环境也可能导致相同的蛋白前体采用不同的淀粉样结构。为了解决组织环境对淀粉样变的结构多态性的影响,我们从一位 AL 患者 (AL55) 的肾脏中提取了纤维,该患者的心脏淀粉样结构先前已被我们小组确定。在这里,我们表明肾脏纤维的 4.0Å 分辨率冷冻电镜结构与我们之前报道的心脏纤维结构几乎相同。这些结果提供了第一个结构证据,证明在同一 AL 患者的不同器官中独立沉积的 LC 淀粉样纤维具有共同的折叠。