Most newly synthesized proteins destined for the secretory pathway contain a signal peptide (SP) that triggers cotranslational translocation into the endoplasmic reticulum (ER). However, how small polypeptides undergo ER translocation is not fully understood. In this issue of , Guo describe a mechanism for posttranslational translocation of small secretory proteins featuring a positive charge within the SP N-terminal region. Defects in this element disrupt proper secretion and explain the effects of genetic mutations associated with one type of diabetes.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5808754 | PMC |
http://dx.doi.org/10.1074/jbc.H118.001415 | DOI Listing |
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