Englert Judson M, Ramsgaard Lasse, Valnickova Zuzana, Enghild Jan J, Oury Tim D
Department of Pathology, University of Pittsburgh School of Medicine, 200 Lothrop Street, W957 BST, Pittsburgh, PA 15261, USA.
Protein Expr Purif. 2008 Sep;61(1):99-101. doi: 10.1016/j.pep.2008.05.004. Epub 2008 May 20.
The receptor for advanced glycation end-products (RAGE) has been implicated in numerous disease processes including: atherosclerosis, diabetic nephropathy, impaired wound healing and neuropathy to name a few. Treatment of animals with a soluble isoform of the receptor (sRAGE) has been shown to prevent and even reverse many disease processes. Isolating large quantities of pure sRAGE for in vitro and in vivo studies has hindered its development as a therapeutic strategy in other RAGE mediated diseases that require long-term therapy. This article provides an improvement in both yield and detail of a previously published method to obtain 10mg of pure, endotoxin free sRAGE from 65 g of lung tissue.
晚期糖基化终产物受体(RAGE)与多种疾病进程相关,包括动脉粥样硬化、糖尿病肾病、伤口愈合受损和神经病变等。已证明用该受体的可溶性异构体(sRAGE)治疗动物可预防甚至逆转许多疾病进程。分离大量纯sRAGE用于体外和体内研究阻碍了其作为一种治疗策略在其他需要长期治疗的RAGE介导疾病中的发展。本文改进了先前发表的一种方法,该方法可从65克肺组织中获得10毫克纯的、无内毒素的sRAGE,提高了产量并细化了细节。