Ghafouri Mehrnoosh, Gauss Chester B, Fribley Andrew M
Carman and Ann Adams Department of Pediatrics, Wayne State University School of Medicine, Detroit, MI, USA.
Department of Otolaryngology-Head and Neck Surgery, Wayne State University School of Medicine, Detroit, MI, USA.
Methods Mol Biol. 2022;2378:317-327. doi: 10.1007/978-1-0716-1732-8_20.
The identification of small molecules and natural product extracts that enhance or interfere with the productivity of protein folding in the endoplasmic reticulum (ER) has the potential to improve a wide variety of human pathologies. Every protein that is destined for a lysosome, integral to the cell membrane, or secreted, is folded, post-translationally modified, and exported to the cytoplasm from the ER-Golgi complex. The following protocols have successfully employed several high-fidelity cell-based luciferase high-throughput screens (HTS) to identify activators and inhibitors of ER stress and the unfolded protein response (UPR).
鉴定能够增强或干扰内质网(ER)中蛋白质折叠效率的小分子和天然产物提取物,有可能改善多种人类疾病。每一种 destined for a lysosome(此处原文有误,可能是“destined for the lysosome”,即“ destined for the lysosome(靶向溶酶体)”)、整合到细胞膜上或分泌的蛋白质,都会在内质网-高尔基体复合体中进行折叠、翻译后修饰,并输出到细胞质中。以下方案已成功应用了几种基于细胞的高保真荧光素酶高通量筛选(HTS)来鉴定内质网应激和未折叠蛋白反应(UPR)的激活剂和抑制剂。