首页> 外文期刊>Biochemical and Biophysical Research Communications >Expression and purification of the soluble isoform of human receptor for advanced glycation end products (sRAGE) from Pichia pastoris.
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Expression and purification of the soluble isoform of human receptor for advanced glycation end products (sRAGE) from Pichia pastoris.

机译:巴斯德毕赤酵母晚期糖基化终产物(sRAGE)的人类受体可溶性亚型的表达和纯化。

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摘要

RAGE is a multi-ligand receptor involved in various human diseases including diabetes, cancer or Alzheimer's disease. Engagement of RAGE by its ligands triggers activation of key cellular signalling pathways such as the MAP kinase and NF-kappaB pathways. Whereas the main isoform of RAGE is a transmembrane receptor with both extra- and intracellular domains, a secreted soluble isoform (sRAGE), corresponding to the extracellular part only, has the ability to block RAGE signalling and suppress cellular activation. Administration of sRAGE to animal models of cancer or multiple sclerosis blocked successfully tumour growth and the course of the autoimmune disease. These findings demonstrate that sRAGE may have a potential as therapeutic. We present here a fast and simple purification protocol of sRAGE from the yeast Pichia pastoris. The identity of the protein was confirmed by mass spectrometry and Western blot. The protein was N-glycosylated and 95-98% pure as judged by SDS-PAGE.
机译:RAGE是一种多配体受体,涉及多种人类疾病,包括糖尿病,癌症或阿尔茨海默氏病。 RAGE与其配体的结合触发了关键细胞信号传导途径(如MAP激酶和NF-κB途径)的激活。 RAGE的主要同工型是具有细胞外和细胞内结构域的跨膜受体,而分泌的可溶性同工型(sRAGE)仅对应于细胞外部分,具有阻断RAGE信号传导和抑制细胞活化的能力。对癌症或多发性硬化症的动物模型施用sRAGE可成功阻断肿瘤生长和自身免疫性疾病的进程。这些发现表明,sRAGE可能具有治疗潜力。我们在这里介绍从酵母毕赤酵母中快速,简便地纯化sRAGE的协议。通过质谱和蛋白质印迹证实了蛋白质的身份。通过SDS-PAGE判断,该蛋白质被N-糖基化并且纯度为95-98%。

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