Raykhel Irina, Alanen Heli, Salo Kirsi, Jurvansuu Jaana, Nguyen Van Dat, Latva-Ranta Maria, Ruddock Lloyd
Department of Biochemistry, Biocenter Oulu, University of Oulu, 90570 Oulu, Finland.
J Cell Biol. 2007 Dec 17;179(6):1193-204. doi: 10.1083/jcb.200705180.
AC-terminal KDEL-like motif prevents secretion of soluble endoplasmic reticulum (ER)-resident proteins. This motif interacts with KDEL receptors localized in the intermediate compartment and Golgi apparatus. Such binding triggers retrieval back to the ER via a coat protein I-dependent pathway. To date, two human KDEL receptors have been reported. Here, we report the Golgi localization of a third human KDEL receptor. Using a reporter construct system from a screen of 152 variants, we identified 35 KDEL-like variants that result in efficient ER localization but do not match the current Prosite motif for ER localization ([KRHQSA]-[DENQ]-E-L). We cloned 16 human proteins with one of these motifs and all were found in the ER. A subsequent screen by bimolecular fluorescence complementation determined the specificities of the three human KDEL receptors. Each KDEL receptor has a unique pattern of motifs with which it interacts. This suggests a specificity in the retrieval of human proteins that contain different KDEL variants.
内质网(ER)驻留蛋白C末端类似KDEL的基序可阻止其分泌。该基序与定位于中间区室和高尔基体的KDEL受体相互作用。这种结合通过依赖于衣被蛋白I的途径触发其返回内质网。迄今为止,已报道了两种人类KDEL受体。在此,我们报道了第三种人类KDEL受体的高尔基体定位。使用来自152个变体筛选的报告构建体系统,我们鉴定出35个类似KDEL的变体,这些变体导致有效的内质网定位,但与当前用于内质网定位的Prosite基序([KRHQSA]-[DENQ]-E-L)不匹配。我们克隆了16种具有这些基序之一的人类蛋白质,并且所有这些蛋白质都在内质网中被发现。随后通过双分子荧光互补进行的筛选确定了三种人类KDEL受体的特异性。每个KDEL受体都有其与之相互作用的独特基序模式。这表明在含有不同KDEL变体的人类蛋白质的回收中存在特异性。