cells part 2. active transport uses atp to move solutes across a membrane requires carrier proteins
TRANSCRIPT
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Cells Part 2
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Active Transport
• Uses ATP to move solutes across a membrane• Requires carrier proteins
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Types of Active Transport
• Symport system – two substances are moved across a membrane in the same direction
• Antiport system – two substances are moved across a membrane in opposite directions
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Types of Active Transport
• Primary active transport – hydrolysis of ATP phosphorylates the transport protein causing conformational change
• Secondary active transport – use of an exchange pump (such as the Na+-K+ pump) indirectly to drive the transport of other solutes
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Types of Active Transport
Figure 3.11
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Vesicular Transport
• Transport of large particles and macromolecules across plasma membranes– Exocytosis – moves substance from the cell
interior to the extracellular space– Endocytosis – enables large particles and
macromolecules to enter the cell
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Vesicular Transport
• Transcytosis – moving substances into, across, and then out of a cell
• Vesicular trafficking – moving substances from one area in the cell to another
• Phagocytosis – pseudopods engulf solids and bring them into the cell’s interior
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Vesicular Transport
• Fluid-phase endocytosis – the plasma membrane infolds, bringing extracellular fluid and solutes into the interior of the cell
• Receptor-mediated endocytosis – clathrin-coated pits provide the main route for endocytosis and transcytosis
• Non-clathrin-coated vesicles – caveolae that are platforms for a variety of signaling molecules
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Exocytosis
Figure 3.12a
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Clathrin-Mediated Endocytosis
Figure 3.13a
Recycling ofmembrane andreceptors (if present)to plasma membrane
CytoplasmExtracellular fluid
Extracellularfluid
Plasmamembrane
Detachmentof clathrin-coatedvesicle
Clathrin-coatedvesicle
Uncoating
Uncoatedvesicle
Uncoatedvesiclefusing withendosome
To lysosomefor digestionand releaseof contents
Transcytosis
Endosome
Exocytosisof vesiclecontents
Clathrin-coatedpit
Plasmamembrane
Ingestedsubstance
Clathrinprotein
(a) Clathrin-mediated endocytosis
2
1
3
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Clathrin-Mediated Endocytosis
Figure 3.13a
CytoplasmExtracellular fluid
Extracellularfluid
Plasmamembrane
Clathrin-coatedpit
Plasmamembrane
Ingestedsubstance
(a) Clathrin-mediated endocytosis
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Clathrin-Mediated Endocytosis
Figure 3.13a
CytoplasmExtracellular fluid
Extracellularfluid
Plasmamembrane
Detachmentof clathrin-coatedvesicle
Clathrin-coatedvesicle
Clathrin-coatedpit
Plasmamembrane
Ingestedsubstance
(a) Clathrin-mediated endocytosis
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Clathrin-Mediated Endocytosis
Figure 3.13a
CytoplasmExtracellular fluid
Extracellularfluid
Plasmamembrane
Detachmentof clathrin-coatedvesicle
Clathrin-coatedvesicle
Uncoating
Uncoatedvesicle
Uncoatedvesiclefusing withendosome
Endosome
Clathrin-coatedpit
Plasmamembrane
Ingestedsubstance
Clathrinprotein
(a) Clathrin-mediated endocytosis
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Clathrin-Mediated Endocytosis
Figure 3.13a
Recycling ofmembrane andreceptors (if present)to plasma membrane
CytoplasmExtracellular fluid
Extracellularfluid
Plasmamembrane
Detachmentof clathrin-coatedvesicle
Clathrin-coatedvesicle
Uncoating
Uncoatedvesicle
Uncoatedvesiclefusing withendosome
Endosome
Clathrin-coatedpit
Plasmamembrane
Ingestedsubstance
Clathrinprotein
(a) Clathrin-mediated endocytosis
1
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Clathrin-Mediated Endocytosis
Figure 3.13a
CytoplasmExtracellular fluid
Extracellularfluid
Plasmamembrane
Detachmentof clathrin-coatedvesicle
Clathrin-coatedvesicle
Uncoating
Uncoatedvesicle
Uncoatedvesiclefusing withendosome
To lysosomefor digestionand releaseof contents
Endosome
Clathrin-coatedpit
Plasmamembrane
Ingestedsubstance
Clathrinprotein
(a) Clathrin-mediated endocytosis
2
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Clathrin-Mediated Endocytosis
Figure 3.13a
CytoplasmExtracellular fluid
Extracellularfluid
Plasmamembrane
Detachmentof clathrin-coatedvesicle
Clathrin-coatedvesicle
Uncoating
Uncoatedvesicle
Uncoatedvesiclefusing withendosome
Transcytosis
Endosome
Exocytosisof vesiclecontents
Clathrin-coatedpit
Plasmamembrane
Ingestedsubstance
Clathrinprotein
(a) Clathrin-mediated endocytosis
3
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Clathrin-Mediated Endocytosis
Figure 3.13a
Recycling ofmembrane andreceptors (if present)to plasma membrane
CytoplasmExtracellular fluid
Extracellularfluid
Plasmamembrane
Detachmentof clathrin-coatedvesicle
Clathrin-coatedvesicle
Uncoating
Uncoatedvesicle
Uncoatedvesiclefusing withendosome
To lysosomefor digestionand releaseof contents
Transcytosis
Endosome
Exocytosisof vesiclecontents
Clathrin-coatedpit
Plasmamembrane
Ingestedsubstance
Clathrinprotein
(a) Clathrin-mediated endocytosis
2
1
3
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Phagocytosis
Figure 3.13b
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Receptor Mediated Endocytosis
Figure 3.13c
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Passive Membrane Transport – Review
Process Energy Source Example
Simple diffusion Kinetic energy Movement of O2 through membrane
Facilitated diffusion Kinetic energy Movement of glucose into cells
Osmosis Kinetic energy Movement of H2O in & out of cells
Filtration Hydrostatic pressure Formation of kidney filtrate
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Active Membrane Transport – Review
Process Energy Source Example
Active transport of solutes ATPMovement of ions across
membranes
Exocytosis ATP Neurotransmitter secretion
Endocytosis ATP White blood cell phagocytosis
Fluid-phase endocytosis ATP Absorption by intestinal cells
Receptor-mediated endocytosis ATP Hormone and cholesterol uptake
Endocytosis via caveoli ATP Cholesterol regulation
Endocytosis via coatomer vesicles
ATP Intracellular trafficking of molecules
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Membrane Potential• Voltage across a membrane• Resting membrane potential – the point where
K+ potential is balanced by the membrane potential– Ranges from –20 to –200 mV– Results from Na+ and K+ concentration gradients
across the membrane– Differential permeability of the plasma membrane
to Na+ and K+
• Steady state – potential maintained by active transport of ions
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Generation and Maintenance of Membrane Potential
PLAY InterActive Physiology ®: Nervous System I: The Membrane Potential
Figure 3.15
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Cell Adhesion Molecules (CAMs)
• Anchor cells to the extracellular matrix• Assist in movement of cells past one another• Rally protective white blood cells to injured or
infected areas
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Roles of Membrane Receptors• Contact signaling – important in normal
development and immunity• Electrical signaling – voltage-regulated “ion
gates” in nerve and muscle tissue• Chemical signaling – neurotransmitters bind to
chemically gated channel-linked receptors in nerve and muscle tissue
• G protein-linked receptors – ligands bind to a receptor which activates a G protein, causing the release of a second messenger, such as cyclic AMP
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Operation of a G Protein
• An extracellular ligand (first messenger), binds to a specific plasma membrane protein
• The receptor activates a G protein that relays the message to an effector protein
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Operation of a G Protein
• The effector is an enzyme that produces a second messenger inside the cell
• The second messenger activates a kinase• The activated kinase can trigger a variety of
cellular responses
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Operation of a G Protein
Figure 3.16
Extracellular fluid
Cytoplasm
Inactivesecondmessenger
Cascade of cellular responses(metabolic and structural changes)
Effector(e.g., enzyme)
Activated(phosphorylated)kinases
First messenger(ligand)
Activesecondmessenger(e.g., cyclicAMP)
Membranereceptor
G protein
1
2
3 4
5
6
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Operation of a G Protein
Figure 3.16
Extracellular fluid
Cytoplasm
First messenger(ligand)
Membranereceptor
1
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Operation of a G Protein
Figure 3.16
Extracellular fluid
Cytoplasm
First messenger(ligand)
Membranereceptor
G protein
1
2
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Operation of a G Protein
Figure 3.16
Extracellular fluid
Cytoplasm
Effector(e.g., enzyme)
First messenger(ligand)
Membranereceptor
G protein
1
2
3
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Operation of a G Protein
Figure 3.16
Extracellular fluid
Cytoplasm
Inactivesecondmessenger
Effector(e.g., enzyme)
First messenger(ligand)
Activesecondmessenger(e.g., cyclicAMP)
Membranereceptor
G protein
1
2
3 4
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Operation of a G Protein
Figure 3.16
Extracellular fluid
Cytoplasm
Inactivesecondmessenger
Effector(e.g., enzyme)
Activated(phosphorylated)kinases
First messenger(ligand)
Activesecondmessenger(e.g., cyclicAMP)
Membranereceptor
G protein
1
2
3 4
5
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Operation of a G Protein
Figure 3.16
Extracellular fluid
Cytoplasm
Inactivesecondmessenger
Cascade of cellular responses(metabolic and structural changes)
Effector(e.g., enzyme)
Activated(phosphorylated)kinases
First messenger(ligand)
Activesecondmessenger(e.g., cyclicAMP)
Membranereceptor
G protein
1
2
3 4
5
6
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Cytoplasm
• Cytoplasm – material between plasma membrane and the nucleus
• Cytosol – largely water with dissolved protein, salts, sugars, and other solutes
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Cytoplasm
• Cytoplasmic organelles – metabolic machinery of the cell
• Inclusions – chemical substances such as glycosomes, glycogen granules, and pigment
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Cytoplasmic Organelles
• Specialized cellular compartments• Membranous – Mitochondria, peroxisomes, lysosomes,
endoplasmic reticulum, and Golgi apparatus• Nonmembranous– Cytoskeleton, centrioles, and ribosomes
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Mitochondria
• Double membrane structure with shelf-like cristae
• Provide most of the cell’s ATP via aerobic cellular respiration
• Contain their own DNA and RNA
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Mitochondria
Figure 3.17a, b
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Ribosomes
• Granules containing protein and rRNA• Site of protein synthesis• Free ribosomes synthesize soluble proteins• Membrane-bound ribosomes synthesize
proteins to be incorporated into membranes
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Endoplasmic Reticulum (ER)
• Interconnected tubes and parallel membranes enclosing cisternae
• Continuous with the nuclear membrane• Two varieties – rough ER and smooth ER
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Endoplasmic Reticulum (ER)
Figure 3.18a, c
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Rough (ER)
• External surface studded with ribosomes• Manufactures all secreted proteins• Responsible for the synthesis of integral
membrane proteins and phospholipids for cell membranes
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Signal Mechanism of Protein Synthesis
• mRNA – ribosome complex is directed to rough ER by a signal-recognition particle (SRP)
• SRP is released and polypeptide grows into cisternae
• The protein is released into the cisternae and sugar groups are added
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Signal Mechanism of Protein Synthesis
• The protein folds into a three-dimensional conformation
• The protein is enclosed in a transport vesicle and moves toward the Golgi apparatus
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Signal Mechanism of Protein Synthesis
Figure 3.19
Cytosol
Ribosomes
mRNA
Coatomer-coatedtransportvesicle
Transportvesiclebudding off
Releasedglycoprotein
ERcisterna
ERmembrane
Signal-recognitionparticle(SRP)
Signalsequence
Receptorsite
Sugargroup
SignalsequenceremovedGrowing
polypeptide
1
2
34
5
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Signal Mechanism of Protein Synthesis
Figure 3.19
Cytosol
mRNA
ERcisterna
ERmembrane
Signal-recognitionparticle(SRP)
Signalsequence
Receptorsite
1
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Signal Mechanism of Protein Synthesis
Figure 3.19
Cytosol
mRNA
ERcisterna
ERmembrane
Signal-recognitionparticle(SRP)
Signalsequence
Receptorsite Growing
polypeptide
1
2
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Signal Mechanism of Protein Synthesis
Figure 3.19
Cytosol
Ribosomes
mRNA
ERcisterna
ERmembrane
Signal-recognitionparticle(SRP)
Signalsequence
Receptorsite
SignalsequenceremovedGrowing
polypeptide
1
2
3
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Signal Mechanism of Protein Synthesis
Figure 3.19
Cytosol
Ribosomes
mRNA
Releasedglycoprotein
ERcisterna
ERmembrane
Signal-recognitionparticle(SRP)
Signalsequence
Receptorsite
SignalsequenceremovedGrowing
polypeptide
1
2
34
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Signal Mechanism of Protein Synthesis
Figure 3.19
Cytosol
Ribosomes
mRNA
Transportvesiclebudding off
Releasedglycoprotein
ERcisterna
ERmembrane
Signal-recognitionparticle(SRP)
Signalsequence
Receptorsite
Sugargroup
SignalsequenceremovedGrowing
polypeptide
1
2
34
5
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Signal Mechanism of Protein Synthesis
Figure 3.19
Cytosol
Ribosomes
mRNA
Coatomer-coatedtransportvesicle
Transportvesiclebudding off
Releasedglycoprotein
ERcisterna
ERmembrane
Signal-recognitionparticle(SRP)
Signalsequence
Receptorsite
Sugargroup
SignalsequenceremovedGrowing
polypeptide
1
2
34
5
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Smooth ER• Tubules arranged in a looping network• Catalyzes the following reactions in various
organs of the body– In the liver – lipid and cholesterol metabolism,
breakdown of glycogen and, along with the kidneys, detoxification of drugs
– In the testes – synthesis of steroid-based hormones
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Smooth ER• Catalyzes the following reactions in various
organs of the body (continued)– In the intestinal cells – absorption, synthesis, and
transport of fats– In skeletal and cardiac muscle – storage and
release of calcium