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Unit 6: The Endomembrane System and Protein Trafficking

How a cell addresses, folds, modifies, and ships every protein it makes to the exact compartment it belongs in, one vesicle at a time.

8 topics · 31 questions

Each topic is a path, not a menu: work down it in order and every question builds on the one above. Click any of them to watch the answer draw itself.

Signal Sequences and Protein Sorting Decisions

  1. How it worksHow does a short stretch of amino acids at a protein's tip act as its zip code to a destination inside the cell?
  2. How it worksWalk me through how a signal recognition particle intercepts a ribosome making a secretory protein.
  3. Common mistakeWhy doesn't every protein made in the cytosol automatically end up outside the cell?
  4. Going furtherWhat happens to a protein's destination when its signal sequence is experimentally deleted?
Your turn1 of 2
A protein is being synthesized on a free ribosome in the cytosol. A student assumes that because translation happens in the cytosol, the finished protein will automatically be secreted outside the cell. Why is this wrong?

Co-translational Translocation into the Rough ER

  1. How it worksHow does the signal recognition particle dock a translating ribosome onto the ER's translocon channel?
  2. How it worksWalk me through how the growing polypeptide threads through the translocon pore into the ER lumen as translation continues.
  3. Common mistakeWhy isn't every protein synthesized on a ribosome attached to the rough ER?
  4. Going furtherWhat happens to a membrane protein's orientation when a stop-transfer sequence halts it partway through the translocon?
Your turn1 of 2
A student assumes that because ribosomes can dock onto the rough ER, every ribosome in the cell eventually ends up attached there. Why isn't every protein synthesized on a ribosome attached to the rough ER?

Protein Folding and Quality Control in the ER

  1. How it worksHow do ER chaperones like BiP recognize and hold onto an incompletely folded protein?
  2. How it worksHow does glycosylation act as a timer that tags a protein for another folding attempt or for destruction?
  3. Common mistakeWhy doesn't a protein that fails ER quality control simply get released into the cytosol unmodified?
  4. Ties togetherHow does ER-associated degradation connect the endomembrane system to the cytosol's own protein-destruction machinery?
Your turn1 of 2
A newly made protein in the ER fails quality control because it hasn't folded correctly. A student assumes the ER simply lets such proteins leak out into the cytosol unmodified once folding attempts stop. What actually happens instead?

The Golgi Apparatus and Sequential Protein Modification

  1. How it worksHow do proteins move from the cis face to the trans face of the Golgi while enzymes modify them along the way?
  2. How it worksWalk me through how the Golgi sorts finished proteins into different vesicles addressed to different destinations.
  3. Common mistakeWhy isn't the Golgi apparatus just a passive tunnel that proteins pass through unchanged?
  4. Going furtherWhat happens to a protein's final sugar structure when a specific Golgi enzyme is missing?
Your turn1 of 2
A protein enters the Golgi apparatus at its cis face and exits at its trans face carrying a very different set of attached sugars than it had when it entered. A student assumes the Golgi is just a passive tunnel proteins pass through unchanged. Why is this wrong?

Vesicle Coats: COPII, COPI, and Clathrin

  1. How it worksHow does a COPII coat select and concentrate cargo while pulling the ER membrane into a bud?
  2. How it worksHow does a clathrin coat form a lattice that pinches a vesicle off the plasma membrane?
  3. Common mistakeWhy doesn't a vesicle keep its coat all the way until it fuses with its target membrane?
  4. Going furtherWhat happens to ER-to-Golgi transport when the gene for a COPII coat protein is knocked out?
Your turn1 of 2
A vesicle buds off the ER wearing a COPII coat. A student assumes that coat stays on the vesicle all the way until it fuses with the Golgi. Why isn't that what actually happens?

SNARE Proteins and the Specificity of Membrane Fusion

  1. How it worksHow do complementary v-SNARE and t-SNARE proteins zipper together to pull two membranes into fusion?
  2. Common mistakeWhy isn't vesicle fusion driven by chance collision between a vesicle and any nearby membrane?
  3. Going furtherWhat happens to neurotransmitter release when a toxin like botulinum cleaves a SNARE protein?
Your turn1 of 2
A vesicle budding from the ER reliably fuses only with the Golgi and never with a lysosome, even though both organelles are nearby in the cell. A student assumes this specificity comes down to which membrane the vesicle happens to bump into by chance. Why is this wrong?

Lysosomes, Endocytosis, and Intracellular Digestion

  1. How it worksHow does a lysosome pump protons into itself to reach the acidic pH its enzymes need?
  2. How it worksWalk me through how a cell surrounds a bound ligand at its surface and pulls it inward as an endocytic vesicle.
  3. How it worksHow does an endosome mature into a lysosome as it acidifies and picks up digestive enzymes?
  4. Common mistakeWhy doesn't a lysosome's own membrane get digested by the enzymes it contains?
  5. Going furtherWhat happens to a cell's ability to clear damaged organelles when a lysosomal storage enzyme is missing?
Your turn1 of 2
A lysosome is packed with enzymes capable of digesting proteins, lipids, and nucleic acids, yet its own membrane remains intact. Why doesn't a lysosome digest itself with the enzymes it contains?

Exocytosis and Regulated Secretion

  1. How it worksHow does a rise in intracellular calcium trigger a docked secretory vesicle to fuse with the plasma membrane?
  2. Common mistakeWhy isn't regulated secretion the same process as the constant, unregulated exocytosis that maintains the plasma membrane?
  3. Going furtherWhat happens to hormone release when the calcium signal that triggers vesicle fusion never arrives?
Your turn1 of 2
A pancreatic cell continuously inserts new membrane proteins into its plasma membrane through ongoing exocytosis, while separately holding thousands of insulin-packed vesicles in reserve until a specific signal arrives. A student assumes these are the same kind of exocytosis happening at different speeds. Why is this wrong?