Questions and Answers
What is a key step that distinguishes regulated exocytosis from constitutive exocytosis?
Which proteins are required for the formation of trans-SNARE complexes during vesicle fusion?
What initiates the degranulation process in granulocytes and mast cells?
Which small GTPases are involved in the regulation of vesicle formation from the donor membrane?
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In polarized cells, what determines the selective delivery of molecules from the TGN to the plasma membrane?
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What process involves bringing molecules and other substances into the cell?
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Which of the following is NOT a step in the process of constitutive exocytosis?
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What type of vesicles mediates transport between the Golgi and plasma membrane?
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What is a key feature of regulated exocytosis compared to constitutive exocytosis?
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What initiates the recruitment of coat proteins to membranes for vesicle budding?
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What defines a polyprotein in the context of secretory vesicles?
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What is the primary role of adaptor proteins in the formation of coated vesicles?
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In which part of the cell does the proteolysis of inactive precursors begin?
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What role do ADP-ribosylation factor (ARF) GTPases play in vesicle transport?
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Which proteins are responsible for the interaction during the fusion of vesicles with target membranes?
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What is the primary function of dynamin during vesicle formation?
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How are transport vesicles guided to their target membranes?
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What happens to the coat of a vesicle after it is released from the donor membrane?
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What defines the polarized sorting of proteins in epithelial cells?
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What initiates the fusion of secretory vesicles with target membranes?
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Which feature distinguishes apical plasma membranes in polarized epithelial cells?
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What is the primary distinction in the function of exocytosis compared to endocytosis?
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Which step is unique to regulated exocytosis and not part of constitutive exocytosis?
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What is the role of coat proteins in vesicle formation?
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Which type of coat is specifically associated with retrograde transport between the ER and Golgi?
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What is the initial destination of soluble proteins from the Golgi in unpolarized cells if they are not retained in the ER or Golgi?
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How do transport vesicles travel to the cell membrane?
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What triggers the release of vesicle contents into the extracellular space during exocytosis?
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What is the method by which vesicles bud off from the plasma membrane?
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What happens to the coat of a coated vesicle once it is formed and released?
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Which of the following best describes a polyprotein in the context of secretory vesicles?
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What triggers the release of cargo from secretory vesicles during exocytosis?
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Which additional step is involved in regulated exocytosis compared to constitutive exocytosis?
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In polarized cells, what does the transport from the TGN selectively deliver?
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What type of cells utilize directed exocytosis to release perforin and granzymes?
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Which GTPase is involved in the docking and tethering process of vesicles?
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What regulates the formation of coated vesicles during vesicle budding?
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What is the main purpose of degranulation in granulocytes and mast cells?
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What does the vesicle 'coat' do during vesicle budding?
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What role do v-SNAREs and t-SNAREs play in vesicle transport?
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What is a key characteristic of regulated exocytosis?
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What role do small GTPases such as ARF and Sar1 play in vesicle transport?
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Which component is responsible for the final pinching-off of a budding vesicle?
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What is the importance of SNARE proteins in the vesicular transport process?
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How do vesicles identify their target membranes during transport?
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Which type of membrane proteins are enriched in the apical plasma membrane of polarized epithelial cells?
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What signals the regulated exocytosis process in secretory vesicles?
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Which type of vesicle is involved in the transport from the Golgi to the endoplasmic reticulum?
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What triggers the loss of the clathrin coat from a vesicle?
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What describes the role of Rab GTPases in vesicular transport?
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What happens to the water molecules during the fusion of vesicles?
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What is the primary function of Sar1 in vesicle transport?
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Which type of proteins are responsible for recognizing sorting signals in polarized epithelial cells?
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What mechanism allows for the fusion of vesicles with their target membranes?
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Which enzyme is primarily responsible for the removal of the coat from vesicles after they bud off?
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Which process is triggered by a chemical messenger leading to the release of secretory vesicle cargo?
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What type of membrane proteins are primarily associated with lipid rafts in the apical plasma membrane?
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Which GTPase is specifically involved in recruiting coat proteins during vesicle formation?
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During which stage of vesicle transport do microtubules facilitate movement towards target membranes?
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What role does dynamin play in the process of vesicle budding?
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What is the significance of Rab effectors in vesicular transport?
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How does Ca²⁺ play a role in the exocytosis process?
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What step is specific to regulated exocytosis that is not found in constitutive exocytosis?
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What is the function of Rab GTPases in vesicle transport?
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In polarized cells, how is the delivery of molecules from the TGN to the plasma membrane characterized?
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What is the primary mechanism by which cytotoxic T cells kill infected cells?
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What is the main function of exocytosis in cellular processes?
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What initiates the fusion of secretory vesicles with their target membranes?
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What outcome results from the priming step in regulated exocytosis?
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Which of the following defines the 'priming' step in regulated exocytosis?
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What is the role of coat proteins in the vesicle budding process?
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What role do coat proteins play in the processes of vesicle budding?
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What describes the type of exocytosis that occurs in a continuous manner regardless of external signals?
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Which type of vesicle is specifically involved in the retrograde transport between the ER and Golgi?
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In what order do the steps of exocytosis occur?
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Which molecules are commonly released by degranulation in immune cells?
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What happens to the coat proteins after vesicle budding?
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Which component is NOT typically involved in the formation of secretory vesicles?
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What is the purpose of the 'tethering' step in the exocytosis process?
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What distinguishes soluble proteins in unpolarized cells from those in polarized cells regarding their destination?
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Which class of proteins is primarily responsible for recruiting coat proteins during vesicle formation?
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Study Notes
Exocytosis vs. Endocytosis
- Endocytosis facilitates the intake of molecules into cells, with vesicles budding from the plasma membrane.
- Exocytosis involves the expulsion of molecules from cells through the fusion of vesicles with the plasma membrane.
Introduction to Exocytosis
- Exocytosis transports molecules out of the cell by fusing vesicles, originating from intracellular organelles, with the plasma membrane.
- Proteins travel from the trans-Golgi network (TGN) to either lysosomes, secretory vesicles, or directly to the cell surface.
- Two pathways exist: constitutive pathway (continuous secretion) and regulated pathway (in specialized cells).
Steps of Exocytosis
- Four steps for constitutive exocytosis; five for regulated exocytosis including:
- Trafficking: Vesicle transport on microtubules.
- Tethering: Initial contact between the vesicle and cell membrane.
- Docking: Attachment of vesicle to cell membrane.
- Priming: Unique to regulated exocytosis, preparing vesicle for fusion.
- Fusion: Complete merging of vesicle and cell membranes releasing contents.
Coated Vesicles
- Vesicle budding is driven by protein coats that cycle on and off membranes.
- Coats contain adaptor proteins for cargo recognition and cage proteins that form a lattice to gather complexes.
- Coat proteins, such as clathrin, COPI, and COPII, facilitate transport between the Golgi, ER, and plasma membrane.
Formation of Secretory Vesicles
- Hormones and enzymes often start as inactive precursors that are activated by proteolysis within vesicles.
- Pre-pro-proteins have an ER signal peptide that is cleaved during synthesis in the rER.
- Signaling molecules can consist of multiple copies of an amino acid sequence forming polyproteins.
Sorting Signals
- In polarized epithelial cells, proteins are sorted in the TGN for specific plasma membrane domains.
- Basolateral membrane proteins have unique signals recognized by coat proteins; apical membranes contain glycosphingolipids and GPI-anchored proteins.
Coat Assembly GTPases
- ARF and Sar1 are small GTPases that recruit coat proteins and regulate vesicular transport.
- Sar1 is crucial for COPII vesicle-mediated transport from ER to Golgi.
- ARF1 plays a role in COPI-mediated transport back to the ER and in clathrin recruitment.
Pinching-off and Uncoating
- Dynamin assembles into a ring around the neck of budding vesicles, facilitating membrane destabilization.
- The clathrin coat is removed after vesicle release, aided by an uncoating ATPase.
Transport, Tethering, Docking
- Vesicle movement is powered by kinesin/dynein and myosin motors.
- Surface markers on vesicles allow recognition by target membranes, regulated by SNAREs and Rab GTPases.
- Rab effectors mediate the tethering and docking process at target membranes.
Fusion
- Docking allows proteins on both membrane bilayers to interact.
- Successful fusion displaces water from the membrane surfaces, enabling merging.
- Trans-SNARE complexes form when v-SNAREs and t-SNAREs interact, pulling membranes together and facilitating fusion.
Release of Secretory Vesicle Cargo
- In regulated exocytosis, secretory vesicles require priming before cargo release, triggered by specific signals like hormonal influx.
- At nerve terminals, action potentials cause Ca²⁺ influx, initiating vesicle fusion and content release.
Overview of Exocytosis
- Exocytosis can be constitutive or regulated, with secretory proteins evolving during vesicle maturation.
- Requires a sequence of steps: trafficking, tethering, docking, fusion, and, in regulated cases, priming.
- Polarized cells ensure selective transport to specific plasma membrane domains, utilizing small GTPases for regulation.
Mechanisms to Kill Cancer Cells
- Degranulation enables the release of cytotoxic molecules from secretory vesicles in immune cells.
- Used by granulocytes, mast cells, natural killer (NK) cells, and cytotoxic T cells to eliminate pathogens and cancer cells.
- Directed exocytosis facilitates the release of perforin and granzymes critical for targeting and destroying infected or cancerous cells.
Exocytosis vs. Endocytosis
- Endocytosis facilitates the intake of molecules into cells, with vesicles budding from the plasma membrane.
- Exocytosis involves the expulsion of molecules from cells through the fusion of vesicles with the plasma membrane.
Introduction to Exocytosis
- Exocytosis transports molecules out of the cell by fusing vesicles, originating from intracellular organelles, with the plasma membrane.
- Proteins travel from the trans-Golgi network (TGN) to either lysosomes, secretory vesicles, or directly to the cell surface.
- Two pathways exist: constitutive pathway (continuous secretion) and regulated pathway (in specialized cells).
Steps of Exocytosis
- Four steps for constitutive exocytosis; five for regulated exocytosis including:
- Trafficking: Vesicle transport on microtubules.
- Tethering: Initial contact between the vesicle and cell membrane.
- Docking: Attachment of vesicle to cell membrane.
- Priming: Unique to regulated exocytosis, preparing vesicle for fusion.
- Fusion: Complete merging of vesicle and cell membranes releasing contents.
Coated Vesicles
- Vesicle budding is driven by protein coats that cycle on and off membranes.
- Coats contain adaptor proteins for cargo recognition and cage proteins that form a lattice to gather complexes.
- Coat proteins, such as clathrin, COPI, and COPII, facilitate transport between the Golgi, ER, and plasma membrane.
Formation of Secretory Vesicles
- Hormones and enzymes often start as inactive precursors that are activated by proteolysis within vesicles.
- Pre-pro-proteins have an ER signal peptide that is cleaved during synthesis in the rER.
- Signaling molecules can consist of multiple copies of an amino acid sequence forming polyproteins.
Sorting Signals
- In polarized epithelial cells, proteins are sorted in the TGN for specific plasma membrane domains.
- Basolateral membrane proteins have unique signals recognized by coat proteins; apical membranes contain glycosphingolipids and GPI-anchored proteins.
Coat Assembly GTPases
- ARF and Sar1 are small GTPases that recruit coat proteins and regulate vesicular transport.
- Sar1 is crucial for COPII vesicle-mediated transport from ER to Golgi.
- ARF1 plays a role in COPI-mediated transport back to the ER and in clathrin recruitment.
Pinching-off and Uncoating
- Dynamin assembles into a ring around the neck of budding vesicles, facilitating membrane destabilization.
- The clathrin coat is removed after vesicle release, aided by an uncoating ATPase.
Transport, Tethering, Docking
- Vesicle movement is powered by kinesin/dynein and myosin motors.
- Surface markers on vesicles allow recognition by target membranes, regulated by SNAREs and Rab GTPases.
- Rab effectors mediate the tethering and docking process at target membranes.
Fusion
- Docking allows proteins on both membrane bilayers to interact.
- Successful fusion displaces water from the membrane surfaces, enabling merging.
- Trans-SNARE complexes form when v-SNAREs and t-SNAREs interact, pulling membranes together and facilitating fusion.
Release of Secretory Vesicle Cargo
- In regulated exocytosis, secretory vesicles require priming before cargo release, triggered by specific signals like hormonal influx.
- At nerve terminals, action potentials cause Ca²⁺ influx, initiating vesicle fusion and content release.
Overview of Exocytosis
- Exocytosis can be constitutive or regulated, with secretory proteins evolving during vesicle maturation.
- Requires a sequence of steps: trafficking, tethering, docking, fusion, and, in regulated cases, priming.
- Polarized cells ensure selective transport to specific plasma membrane domains, utilizing small GTPases for regulation.
Mechanisms to Kill Cancer Cells
- Degranulation enables the release of cytotoxic molecules from secretory vesicles in immune cells.
- Used by granulocytes, mast cells, natural killer (NK) cells, and cytotoxic T cells to eliminate pathogens and cancer cells.
- Directed exocytosis facilitates the release of perforin and granzymes critical for targeting and destroying infected or cancerous cells.
Exocytosis vs. Endocytosis
- Endocytosis facilitates the intake of molecules into cells, with vesicles budding from the plasma membrane.
- Exocytosis involves the expulsion of molecules from cells through the fusion of vesicles with the plasma membrane.
Introduction to Exocytosis
- Exocytosis transports molecules out of the cell by fusing vesicles, originating from intracellular organelles, with the plasma membrane.
- Proteins travel from the trans-Golgi network (TGN) to either lysosomes, secretory vesicles, or directly to the cell surface.
- Two pathways exist: constitutive pathway (continuous secretion) and regulated pathway (in specialized cells).
Steps of Exocytosis
- Four steps for constitutive exocytosis; five for regulated exocytosis including:
- Trafficking: Vesicle transport on microtubules.
- Tethering: Initial contact between the vesicle and cell membrane.
- Docking: Attachment of vesicle to cell membrane.
- Priming: Unique to regulated exocytosis, preparing vesicle for fusion.
- Fusion: Complete merging of vesicle and cell membranes releasing contents.
Coated Vesicles
- Vesicle budding is driven by protein coats that cycle on and off membranes.
- Coats contain adaptor proteins for cargo recognition and cage proteins that form a lattice to gather complexes.
- Coat proteins, such as clathrin, COPI, and COPII, facilitate transport between the Golgi, ER, and plasma membrane.
Formation of Secretory Vesicles
- Hormones and enzymes often start as inactive precursors that are activated by proteolysis within vesicles.
- Pre-pro-proteins have an ER signal peptide that is cleaved during synthesis in the rER.
- Signaling molecules can consist of multiple copies of an amino acid sequence forming polyproteins.
Sorting Signals
- In polarized epithelial cells, proteins are sorted in the TGN for specific plasma membrane domains.
- Basolateral membrane proteins have unique signals recognized by coat proteins; apical membranes contain glycosphingolipids and GPI-anchored proteins.
Coat Assembly GTPases
- ARF and Sar1 are small GTPases that recruit coat proteins and regulate vesicular transport.
- Sar1 is crucial for COPII vesicle-mediated transport from ER to Golgi.
- ARF1 plays a role in COPI-mediated transport back to the ER and in clathrin recruitment.
Pinching-off and Uncoating
- Dynamin assembles into a ring around the neck of budding vesicles, facilitating membrane destabilization.
- The clathrin coat is removed after vesicle release, aided by an uncoating ATPase.
Transport, Tethering, Docking
- Vesicle movement is powered by kinesin/dynein and myosin motors.
- Surface markers on vesicles allow recognition by target membranes, regulated by SNAREs and Rab GTPases.
- Rab effectors mediate the tethering and docking process at target membranes.
Fusion
- Docking allows proteins on both membrane bilayers to interact.
- Successful fusion displaces water from the membrane surfaces, enabling merging.
- Trans-SNARE complexes form when v-SNAREs and t-SNAREs interact, pulling membranes together and facilitating fusion.
Release of Secretory Vesicle Cargo
- In regulated exocytosis, secretory vesicles require priming before cargo release, triggered by specific signals like hormonal influx.
- At nerve terminals, action potentials cause Ca²⁺ influx, initiating vesicle fusion and content release.
Overview of Exocytosis
- Exocytosis can be constitutive or regulated, with secretory proteins evolving during vesicle maturation.
- Requires a sequence of steps: trafficking, tethering, docking, fusion, and, in regulated cases, priming.
- Polarized cells ensure selective transport to specific plasma membrane domains, utilizing small GTPases for regulation.
Mechanisms to Kill Cancer Cells
- Degranulation enables the release of cytotoxic molecules from secretory vesicles in immune cells.
- Used by granulocytes, mast cells, natural killer (NK) cells, and cytotoxic T cells to eliminate pathogens and cancer cells.
- Directed exocytosis facilitates the release of perforin and granzymes critical for targeting and destroying infected or cancerous cells.
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Description
Explore the mechanisms of exocytosis and endocytosis in this quiz from Module 16. Understand how these processes function in transporting molecules in and out of cells, including the role of vesicles and proteins involved. Test your knowledge on these essential cellular activities.