BIOL 201 Lecture Notes - Lecture 19: Phospholipid, Proinsulin, Clathrin

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27 Feb 2014
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The lysosome is the organelle for degradation of different components, especially proteins and lipids which enter the cell and can be broken down into their constituents. Proteins destined for lysosome have internal signals that are recognised by an enzyme in the cis-golgi which attaches to a phosphate group on the manos sugar. This serves as a signal to target the protein to the lysosome. Targeting occurs through a membrane protein located in the trans-golgi-network, manos- In tgn, lysosomal proteins with m6p modification bind to m6p receptor. Ap1- clathrin complex assembles at m6p receptor mediated by arf: clathrin coated vesicle buds from trans- Golgi, coat dissociates: vesicle fuses with late endosome, low ph leads to protein dissociation from receptor, receptor vesicle re-fuses with trans-golgi, transport vesicle fuses with lysosome, many secreted proteins (such as insulin) are synthesized as large. Insulin is synthesized as pre-pro-insulin, which is converted to proinsulin in the er.

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