Unknown

Dataset Information

0

A molecular specificity code for the three mammalian KDEL receptors.


ABSTRACT: 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.

SUBMITTER: Raykhel I 

PROVIDER: S-EPMC2140024 | biostudies-literature | 2007 Dec

REPOSITORIES: biostudies-literature

altmetric image

Publications

A molecular specificity code for the three mammalian KDEL receptors.

Raykhel Irina I   Alanen Heli H   Salo Kirsi K   Jurvansuu Jaana J   Nguyen Van Dat VD   Latva-Ranta Maria M   Ruddock Lloyd L  

The Journal of cell biology 20071201 6


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 3  ...[more]

Similar Datasets

| S-EPMC9220330 | biostudies-literature
| S-EPMC8196686 | biostudies-literature
| S-EPMC4926219 | biostudies-literature
| S-EPMC4442004 | biostudies-literature
| S-EPMC7336508 | biostudies-literature
| S-EPMC6374074 | biostudies-literature
| S-EPMC2206014 | biostudies-literature
| S-EPMC4974620 | biostudies-literature
| S-EPMC3567670 | biostudies-literature
| S-EPMC7961839 | biostudies-literature