1. The individual compartments have different functions due to the unique profile of proteins in these compartments. How do the proteins reach their correct destinations? Where is the information for destination stored? How is this information read? What are the trafficking patterns?

2. Cellular addresses of proteins reside in the primary and secondary structure Cellular sentinels recognize these addresses by direct interaction.

5. 1.Label nascent proteins with radioactive a.a. 2.Homogenize  vesicles 3.Digest +/- detergent 4.SDS PAGE Co-translation Prove it!

6. Secretory proteins move from the rough ER lumen through the Golgi and then to the cell surface. 1.Transport vesicles 2.Cisternal progression 3.TGN 4.Regulated and constitutive secretion 5.Lysozomes

7. Many of the molecules involved in this process were obtained either via genetic or biochemical approaches. But, before that, the pathway had to be discovered and carefully characterized. George Palade got the prize for doing this! see Classic Expt. 17.1 Pulse-chase using acinar cells.

8. Read Classic Experiment 17.1 TS invertase mutants do not secrete invertase at the nonpermissive temperature. Pulse chase experiments were used to identify were secretion was blocked. Analysis of such mutants revealed 5 classes. Cloned genes indicated molecular components of the secretory pathway

9. Translocation of secretory proteins across the ER Signal Sequence Microsomes required Signal sequence cleaved Signal peptidase in lumen SS= charge/hydrophob/charged ca. 70 amino acids from add-in A few are different (alpha factor) This expt. enabled discovery of factors such as the SRP

10. 40 30 (1)300-bp RNA plus (6) subunits SRP relieves stall

11. Chem.-modified lysyl tRNA

13. Orientation of membrane proteins is established during co-translation.