Membrane Transport Active Processes Two types of active

Membrane Transport: Active Processes • Two types of active processes – Active transport – Vesicular transport • Both require ATP to move solutes across a living plasma membrane because – Solute too large for channels – Solute not lipid soluble – Solute not able to move down concentration gradient © 2013 Pearson Education, Inc.

Active Transport • Requires carrier proteins (solute pumps) – Bind specifically and reversibly with substance • Moves solutes against concentration gradient – Requires energy © 2013 Pearson Education, Inc.

Active Transport: Two Types • Primary active transport – Required energy directly from ATP hydrolysis • Secondary active transport – Required energy indirectly from ionic gradients created by primary active transport © 2013 Pearson Education, Inc.

Primary Active Transport • Energy from hydrolysis of ATP causes shape change in transport protein that "pumps" solutes (ions) across membrane • E. g. , calcium, hydrogen, Na+-K+ pumps © 2013 Pearson Education, Inc.

Primary Active Transport • Sodium-potassium pump – Most well-studied – Carrier (pump) called Na+-K+ ATPase – Located in all plasma membranes – Involved in primary and secondary active transport of nutrients and ions © 2013 Pearson Education, Inc.

Sodium-Potassium Pump • Na+ and K+ channels allow slow leakage down concentration gradients • Na+-K+ pump works as antiporter – Pumps against Na+ and K+ gradients to maintain high intracellular K+ concentration and high extracellular Na+ concentration • Maintains electrochemical gradients essential for functions of muscle and nerve tissues • Allows all cells to maintain fluid volume © 2013 Pearson Education, Inc.

Figure 3. 10 Primary active transport is the process in which solutes are moved across cell membranes against electrochemical gradients using energy supplied directly by ATP. Extracellular fluid Na+–K+ pump K+ ATP-binding site Na+ bound Cytoplasm 1 Three cytoplasmic Na + bind to pump protein. P K+ released 2 Na+ binding promotes hydrolysis of ATP. The energy released during this reaction phosphorylates the pump. 6 Pump protein binds ATP; releases K + to the inside, and Na + sites are ready to bind Na+ again. The cycle repeats. Na+ released K+ bound P Pi K+ 5 K+ binding triggers release of the phosphate. The dephosphorylated pump resumes its original conformation. 3 Phosphorylation causes the pump to change shape, expelling Na+ to the outside. P 4 Two extracellular K + bind to pump. © 2013 Pearson Education, Inc. Slide 1

Figure 3. 10 Primary active transport is the process in which solutes are moved across cell membranes against electrochemical gradients using energy supplied directly by ATP. Extracellular fluid Na+–K+ pump ATP-binding site K+ Cytoplasm 1 Three cytoplasmic Na + bind to pump protein. © 2013 Pearson Education, Inc. Slide 2

Figure 3. 10 Primary active transport is the process in which solutes are moved across cell membranes against electrochemical gradients using energy supplied directly by ATP. Extracellular fluid Na+–K+ pump ATP-binding site K+ Na+ bound Cytoplasm 1 Three cytoplasmic Na + bind to pump protein. P 2 Na+ binding promotes hydrolysis of ATP. The energy released during this reaction phosphorylates the pump. © 2013 Pearson Education, Inc. Slide 3

Figure 3. 10 Primary active transport is the process in which solutes are moved across cell membranes against electrochemical gradients using energy supplied directly by ATP. Extracellular fluid Na+–K+ pump ATP-binding site K+ Na+ bound Cytoplasm 1 Three cytoplasmic Na + bind to pump protein. P 2 Na+ binding promotes hydrolysis of ATP. The energy released during this reaction phosphorylates the pump. Na+ released P 3 Phosphorylation causes the pump to change shape, expelling Na+ to the outside. © 2013 Pearson Education, Inc. Slide 4

Figure 3. 10 Primary active transport is the process in which solutes are moved across cell membranes against electrochemical gradients using energy supplied directly by ATP. Extracellular fluid Na+–K+ pump K+ ATP-binding site Na+ bound Cytoplasm 1 Three cytoplasmic Na + bind to pump protein. P 2 Na+ binding promotes hydrolysis of ATP. The energy released during this reaction phosphorylates the pump. Na+ released P K+ 3 Phosphorylation causes the pump to change shape, expelling Na+ to the outside. P 4 Two extracellular K + bind to pump. © 2013 Pearson Education, Inc. Slide 5

Figure 3. 10 Primary active transport is the process in which solutes are moved across cell membranes against electrochemical gradients using energy supplied directly by ATP. Extracellular fluid Na+–K+ pump K+ ATP-binding site Na+ bound Cytoplasm 1 Three cytoplasmic Na + bind to pump protein. P 2 Na+ binding promotes hydrolysis of ATP. The energy released during this reaction phosphorylates the pump. Na+ released K+ bound P Pi K+ 5 K+ binding triggers release of the phosphate. The dephosphorylated pump resumes its original conformation. 3 Phosphorylation causes the pump to change shape, expelling Na+ to the outside. P 4 Two extracellular K + bind to pump. © 2013 Pearson Education, Inc. Slide 6

Figure 3. 10 Primary active transport is the process in which solutes are moved across cell membranes against electrochemical gradients using energy supplied directly by ATP. Extracellular fluid Na+–K+ pump K+ ATP-binding site Na+ bound Cytoplasm 1 Three cytoplasmic Na + bind to pump protein. P K+ released 6 Pump protein binds ATP; releases K + to the inside, and Na + sites are ready to bind Na+ again. The cycle repeats. 2 Na+ binding promotes hydrolysis of ATP. The energy released during this reaction phosphorylates the pump. Na+ released K+ bound P Pi K+ 5 K+ binding triggers release of the phosphate. The dephosphorylated pump resumes its original conformation. 3 Phosphorylation causes the pump to change shape, expelling Na+ to the outside. P 4 Two extracellular K + bind to pump. © 2013 Pearson Education, Inc. Slide 7

Figure 3. 10 Primary active transport is the process in which solutes are moved across cell membranes against electrochemical gradients using energy supplied directly by ATP. Extracellular fluid Na+–K+ pump K+ ATP-binding site Na+ bound Cytoplasm 1 Three cytoplasmic Na + bind to pump protein. P K+ released 6 Pump protein binds ATP; releases K + to the inside, and Na + sites are ready to bind Na+ again. The cycle repeats. 2 Na+ binding promotes hydrolysis of ATP. The energy released during this reaction phosphorylates the pump. Na+ released K+ bound P Pi K+ 5 K+ binding triggers release of the phosphate. The dephosphorylated pump resumes its original conformation. 3 Phosphorylation causes the pump to change shape, expelling Na+ to the outside. P 4 Two extracellular K + bind to pump. © 2013 Pearson Education, Inc. PLAY A&P Flix™: Resting Membrane Potential

Secondary Active Transport • Depends on ion gradient created by primary active transport • Energy stored in ionic gradients used indirectly to drive transport of other solutes © 2013 Pearson Education, Inc.

Secondary Active Transport • Cotransport—always transports more than one substance at a time – Symport system: Substances transported in same direction – Antiport system: Substances transported in opposite directions © 2013 Pearson Education, Inc.

Figure 3. 11 Secondary active transport is driven by the concentration gradient created by primary active transport. Extracellular fluid Slide 1 Glucose Na+-K+ pump Na+-glucose symport transporter loads glucose from extracellular fluid Na+-glucose symport transporter releases glucose into the cytoplasm Cytoplasm 1 Primary active transport The ATP-driven Na+-K+ pump stores energy by creating a steep concentration gradient for Na+ entry into the cell. © 2013 Pearson Education, Inc. 2 Secondary active transport As Na+ diffuses back across the membrane through a membrane cotransporter protein, it drives glucose against its concentration gradient into the cell.

Figure 3. 11 Secondary active transport is driven by the concentration gradient created by primary active transport. Extracellular fluid Na+-K+ pump Cytoplasm 1 Primary active transport The ATP-driven Na+-K+ pump stores energy by creating a steep concentration gradient for Na+ entry into the cell. © 2013 Pearson Education, Inc. Slide 2

Figure 3. 11 Secondary active transport is driven by the concentration gradient created by primary active transport. Extracellular fluid Slide 3 Glucose Na+-K+ pump Na+-glucose symport transporter loads glucose from extracellular fluid Na+-glucose symport transporter releases glucose into the cytoplasm Cytoplasm 1 Primary active transport The ATP-driven Na+-K+ pump stores energy by creating a steep concentration gradient for Na+ entry into the cell. © 2013 Pearson Education, Inc. 2 Secondary active transport As Na+ diffuses back across the membrane through a membrane cotransporter protein, it drives glucose against its concentration gradient into the cell.

Vesicular Transport • Transport of large particles, macromolecules, and fluids across membrane in membranous sacs called vesicles • Requires cellular energy (e. g. , ATP) © 2013 Pearson Education, Inc.

Vesicular Transport • Functions: – Exocytosis—transport out of cell – Endocytosis—transport into cell • Phagocytosis, pinocytosis, receptor-mediated endocytosis – Transcytosis—transport into, across, and then out of cell – Vesicular trafficking—transport from one area or organelle in cell to another © 2013 Pearson Education, Inc.

Endocytosis and Transcytosis • Involve formation of protein-coated vesicles • Often receptor mediated, therefore very selective • Some pathogens also hijack for transport into cell • Once vesicle is inside cell it may – Fuse with lysosome – Undergo transcytosis © 2013 Pearson Education, Inc.

Figure 3. 12 Events of endocytosis mediated by protein-coated pits. 1 Coated pit ingests substance. Protein coat (typically clathrin) 2 Protein-coated vesicle detaches. Extracellular fluid Plasma membrane Cytoplasm 3 Coat proteins are recycled to plasma membrane. Transport vesicle Uncoated endocytic vesicle Endosome 4 Uncoated vesicle fuses with a sorting vesicle called an endosome. Lysosome 5 Transport vesicle containing membrane compone -nts moves to the plasma membrane for recycling. 6 Fused vesicle may (a) fuse with lysosome for digestion of its contents, or (b) deliver its contents to the plasma membrane on the opposite side of the cell (transcytosis). © 2013 Pearson Education, Inc. Slide 1

Figure 3. 12 Events of endocytosis mediated by protein-coated pits. 1 Coated pit ingests substance. Protein coat (typically clathrin) © 2013 Pearson Education, Inc. Extracellular fluid Plasma membrane Cytoplasm Slide 2

Figure 3. 12 Events of endocytosis mediated by protein-coated pits. 1 Coated pit ingests substance. Protein coat (typically clathrin) 2 Protein-coated vesicle detaches. © 2013 Pearson Education, Inc. Extracellular fluid Plasma membrane Cytoplasm Slide 3

Figure 3. 12 Events of endocytosis mediated by protein-coated pits. 1 Coated pit ingests substance. Protein coat (typically clathrin) 2 Protein-coated vesicle detaches. © 2013 Pearson Education, Inc. Extracellular fluid Plasma membrane Cytoplasm 3 Coat proteins are recycled to plasma membrane. Slide 4

Figure 3. 12 Events of endocytosis mediated by protein-coated pits. 1 Coated pit ingests substance. Protein coat (typically clathrin) 2 Protein-coated vesicle detaches. Uncoated endocytic vesicle 4 Uncoated vesicle fuses with a sorting vesicle called an endosome. © 2013 Pearson Education, Inc. Extracellular fluid Plasma membrane Cytoplasm 3 Coat proteins are recycled to plasma membrane. Endosome Slide 5

Figure 3. 12 Events of endocytosis mediated by protein-coated pits. 1 Coated pit ingests substance. Protein coat (typically clathrin) 2 Protein-coated vesicle detaches. Extracellular fluid Plasma membrane Cytoplasm 3 Coat proteins are recycled to plasma membrane. Transport vesicle Uncoated endocytic vesicle 4 Uncoated vesicle fuses with a sorting vesicle called an endosome. © 2013 Pearson Education, Inc. Endosome 5 Transport vesicle containing membrane compone -nts moves to the plasma membrane for recycling. Slide 6

Figure 3. 12 Events of endocytosis mediated by protein-coated pits. 1 Coated pit ingests substance. Protein coat (typically clathrin) 2 Protein-coated vesicle detaches. Extracellular fluid Plasma membrane Cytoplasm 3 Coat proteins are recycled to plasma membrane. Transport vesicle Uncoated endocytic vesicle Endosome 4 Uncoated vesicle fuses with a sorting vesicle called an endosome. Lysosome 5 Transport vesicle containing membrane compone -nts moves to the plasma membrane for recycling. 6 Fused vesicle may (a) fuse with lysosome for digestion of its contents, or (b) deliver its contents to the plasma membrane on the opposite side of the cell (transcytosis). © 2013 Pearson Education, Inc. Slide 7

Endocytosis • Phagocytosis – Pseudopods engulf solids and bring them into cell's interior – Form vesicle called phagosome • Used by macrophages and some white blood cells – Move by amoeboid motion • Cytoplasm flows into temporary extensions • Allows creeping © 2013 Pearson Education, Inc.

Figure 3. 13 a Comparison of three types of endocytosis. Receptors Phagosome © 2013 Pearson Education, Inc. Phagocytosis The cell engulfs a large particle by forming projecting pseudopods ("false feet") around it and enclosing it within a membrane sac called a phagosome. The phagosome is combined with a lysosome. Undigested contents remain in the vesicle (now called a residual body) or are ejected by exocytosis. Vesicle may or may not be protein coated but has receptors capable of binding to microorganisms or solid particles.

Endocytosis • Pinocytosis (fluid-phase endocytosis) – Plasma membrane infolds, bringing extracellular fluid and dissolved solutes inside cell • Fuses with endosome – Most cells utilize to "sample" environment – Nutrient absorption in the small intestine – Membrane components recycled back to membrane © 2013 Pearson Education, Inc.

Figure 3. 13 b Comparison of three types of endocytosis. Pinocytosis The cell "gulps" a drop of extracellular fluid containing solutes into tiny vesicles. No receptors are used, so the process is nonspecific. Most vesicles are protein-coated. Vesicle © 2013 Pearson Education, Inc.

Endocytosis • Receptor-mediated endocytosis – Allows specific endocytosis and transcytosis • Cells use to concentrate materials in limited supply – Clathrin-coated pits provide main route for endocytosis and transcytosis • Uptake of enzymes, low-density lipoproteins, iron, insulin, and, unfortunately, viruses, diphtheria, and cholera toxins © 2013 Pearson Education, Inc.

Receptor-Mediated Endocytosis • Different coat proteins – Caveolae • Capture specific molecules (folic acid, tetanus toxin) and use transcytosis • Involved in cell signaling but exact function unknown – Coatomer • Function in vesicular trafficking © 2013 Pearson Education, Inc.

Figure 3. 13 c Comparison of three types of endocytosis. Vesicle © 2013 Pearson Education, Inc. Receptor-mediated endocytosis Extracellular substances bind to specific receptor proteins, enabling the cell to ingest and concentrate specific substances (ligands) in protein-coated vesicles. Ligands may simply be released inside the cell, or combined with a lysosome to digest contents. Receptors are recycled to the plasma membrane in vesicles.

Exocytosis • Usually activated by cell-surface signal or change in membrane voltage • Substance enclosed in secretory vesicle • v-SNAREs ("v" = vesicle) on vesicle find t-SNAREs ("t" = target) on membrane and bind • Functions – Hormone secretion, neurotransmitter release, mucus secretion, ejection of wastes © 2013 Pearson Education, Inc.

Figure 3. 14 Exocytosis. Slide 1 The process of exocytosis Plasma membrane Extracellular SNARE (t-SNARE) fluid Secretory vesicle Vesicle SNARE (v-SNARE) Molecule to be secreted Cytoplasm Fused v- and t-SNAREs © 2013 Pearson Education, Inc. Fusion pore formed 1 The membranebound vesicle migrates to the plasma membrane. 2 There, proteins at the vesicle surface (v -SNAREs) bind with t -SNAREs (plasma membrane proteins). 3 The vesicle and plasma membrane fuse and a pore opens up. 4 Vesicle contents are released to the cell exterior.

Figure 3. 14 Exocytosis. Slide 2 The process of exocytosis Plasma membrane Extracellular SNARE (t-SNARE) fluid Secretory vesicle Vesicle SNARE (v-SNARE) Molecule to be secreted Cytoplasm © 2013 Pearson Education, Inc. 1 The membranebound vesicle migrates to the plasma membrane.

Figure 3. 14 Exocytosis. Slide 3 The process of exocytosis Plasma membrane Extracellular SNARE (t-SNARE) fluid Secretory vesicle Vesicle SNARE (v-SNARE) Molecule to be secreted Cytoplasm Fused v- and t-SNAREs © 2013 Pearson Education, Inc. 1 The membranebound vesicle migrates to the plasma membrane. 2 There, proteins at the vesicle surface (v -SNAREs) bind with t -SNAREs (plasma membrane proteins).

Figure 3. 14 Exocytosis. Slide 4 The process of exocytosis Plasma membrane Extracellular SNARE (t-SNARE) fluid Secretory vesicle Vesicle SNARE (v-SNARE) Molecule to be secreted Cytoplasm Fused v- and t-SNAREs © 2013 Pearson Education, Inc. Fusion pore formed 1 The membranebound vesicle migrates to the plasma membrane. 2 There, proteins at the vesicle surface (v -SNAREs) bind with t -SNAREs (plasma membrane proteins). 3 The vesicle and plasma membrane fuse and a pore opens up.

Figure 3. 14 Exocytosis. Slide 5 The process of exocytosis Plasma membrane Extracellular SNARE (t-SNARE) fluid Secretory vesicle Vesicle SNARE (v-SNARE) Molecule to be secreted Cytoplasm Fused v- and t-SNAREs © 2013 Pearson Education, Inc. Fusion pore formed 1 The membranebound vesicle migrates to the plasma membrane. 2 There, proteins at the vesicle surface (v -SNAREs) bind with t -SNAREs (plasma membrane proteins). 3 The vesicle and plasma membrane fuse and a pore opens up. 4 Vesicle contents are released to the cell exterior.

Figure 3. 14 b Exocytosis. Photomicrograph of a secretory vesicle releasing its contents by exocytosis (100, 000 x) © 2013 Pearson Education, Inc.

Table 3. 2 Active Membrane Transport Processes (1 of 2) © 2013 Pearson Education, Inc.

Table 3. 2 Active Membrane Transport Processes (2 of 2) © 2013 Pearson Education, Inc.

Generation of a Resting Membrane Potential • Resting membrane potential (RMP) – Produced by separation of oppositely charged particles (voltage) across membrane in all cells • Cells described as polarized – Voltage (electrical potential energy) only at membrane • Ranges from – 50 to – 100 m. V in different cells – "–" indicates inside negative relative to outside © 2013 Pearson Education, Inc.

Selective Diffusion Establishes RMP • Electrochemical gradient established – Electro (charge); chemical (ion concentration) • K+ diffuses out of cell through K+ leakage channels, proteins cannot inside cell membrane more negative • K+ attracted back as inner face more negative • K+ equalizes across membrane at – 90 m. V when K+ concentration gradient balanced by electrical gradient = RMP © 2013 Pearson Education, Inc.

Figure 3. 15 The key role of K+ in generating the resting membrane potential. 1 K+ diffuse down their steep concentration gradient (out of the cell) via leakage channels. Loss of K+ results in a negative charge on the inner plasma membrane face. Extracellular fluid + + – Cytoplasm © 2013 Pearson Education, Inc. – Slide 1 – + – Potassium leakage channels + – + – Protein anion (unable to follow K+ through the membrane) 2 K+ also move into the cell because they are attracted to the negative charge established on the inner plasma membrane face. 3 A negative membrane potential (– 90 m. V) is established when the movement of K+ out of the cell equals K+ movement into the cell. At this point, the concentration gradient promoting K+ exit exactly opposes the electrical gradient for K+ entry.

Figure 3. 15 The key role of K+ in generating the resting membrane potential. 1 K+ diffuse down their steep concentration gradient (out of the cell) via leakage channels. Loss of K+ results in a negative charge on the inner plasma membrane face. Extracellular fluid + + – Cytoplasm © 2013 Pearson Education, Inc. – Slide 2 – + – Potassium leakage channels + – + – Protein anion (unable to follow K+ through the membrane)

Figure 3. 15 The key role of K+ in generating the resting membrane potential. 1 K+ diffuse down their steep concentration gradient (out of the cell) via leakage channels. Loss of K+ results in a negative charge on the inner plasma membrane face. Extracellular fluid + + – Cytoplasm © 2013 Pearson Education, Inc. – Slide 3 – + – Potassium leakage channels + – + – Protein anion (unable to follow K+ through the membrane) 2 K+ also move into the cell because they are attracted to the negative charge established on the inner plasma membrane face.

Figure 3. 15 The key role of K+ in generating the resting membrane potential. 1 K+ diffuse down their steep concentration gradient (out of the cell) via leakage channels. Loss of K+ results in a negative charge on the inner plasma membrane face. Extracellular fluid + + – Cytoplasm © 2013 Pearson Education, Inc. – Slide 4 – + – Potassium leakage channels + – + – Protein anion (unable to follow K+ through the membrane) 2 K+ also move into the cell because they are attracted to the negative charge established on the inner plasma membrane face. 3 A negative membrane potential (– 90 m. V) is established when the movement of K+ out of the cell equals K+ movement into the cell. At this point, the concentration gradient promoting K+ exit exactly opposes the electrical gradient for K+ entry.

Selective Diffusion Establishes RMP • In many cells Na+ affects RMP – Attracted into cell due to negative charge RMP to – 70 m. V – Membrane more permeable to K+ than Na+, so K+ primary influence on RMP • Cl– does not influence RMP— concentration and electrical gradients exactly balanced © 2013 Pearson Education, Inc.

Active Transport Maintains Electrochemical Gradients • Na+-K+ pump continuously ejects 3 Na+ from cell and carries 2 K+ in • Steady state maintained because rate of active transport equal to and depends on rate of Na+ diffusion into cell • Neuron and muscle cells "upset" RMP by opening gated Na+ and K+ channels © 2013 Pearson Education, Inc.

Cell-Environment Interactions • Cells interact directly or indirectly by responding to extracellular chemicals • Always involves glycocalyx – Cell adhesion molecules (CAMs) – Plasma membrane receptors – Voltage-gated channel proteins © 2013 Pearson Education, Inc.

Roles of Cell Adhesion Molecules • • • Thousands on approximately every cell in body Anchor to extracellular matrix or each other Assist in movement of cells past one another Attract WBCs to injured or infected areas Stimulate synthesis or degradation of adhesive membrane junctions • Transmit intracellular signals to direct cell migration, proliferation, and specialization © 2013 Pearson Education, Inc.

Roles of Plasma Membrane Receptors • Contact signaling—touching and recognition of cells; e. g. , in normal development and immunity • Chemical signaling—interaction between receptors and ligands (neurotransmitters, hormones, and paracrines) to alter activity of cell proteins (e. g. , enzymes or chemically gated ion channels) – Same ligand can cause different cell responses – Response determined by what receptor linked to inside cell © 2013 Pearson Education, Inc.

Chemical Signaling • Ligand binding receptor structural change protein alteration – Catalytic receptor proteins become activated enzymes – Chemically gated channel-linked receptors open and close ion gates changes in excitability – G protein–linked receptors activate G protein, affecting an ion channel or enzyme, or causing release of internal second messenger, such as cyclic AMP © 2013 Pearson Education, Inc.

Figure 3. 16 G proteins act as middlemen or relays between extracellular first messengers and intracellular second messengers that cause responses within the cell. Slide 1 The sequence described here is like a molecular relay race. Instead of a baton passed from runner to runner, the message (a shape change) is passed from molecule to molecule as it makes its way across the cell membrane from outside to inside the cell. 1 Ligand* (1 st messenger) binds to the receptor. The receptor changes shape and activates. Ligand (1 st Receptor G protein Enzyme messenger) 2 The activated receptor binds to a G protein and activates it. The G protein changes shape (turns “on”), causing it to release GDP and bind GTP (an energy source). 2 nd messenger 3 Activated G protein activates (or inactivates) an effector protein by causing its shape to change. Extracellular fluid Effector protein (e. g. , an enzyme) Ligand Receptor G protein GDP Inactive 2 nd messenger Activated kinase enzymes * Ligands include hormones and neurotransmitters. © 2013 Pearson Education, Inc. 4 Activated effector enzymes catalyze reactions that produce 2 nd messengers in the cell. (Common 2 nd messengers include cyclic AMP and Ca 2+. ) 5 Second messengers activate other enzymes or ion channels. Cyclic AMP typically activates protein kinase enzymes. 6 Kinase enzymes activate other enzymes. Kinase enzymes transfer phosphate groups from ATP to specific proteins and activate a Cascade of cellular responses series of other enzymes that trigger (The amplification effect is various metabolic and structural tremendous. Each enzyme changes in the cell. catalyzes hundreds of reactions. ) Intracellular fluid

Figure 3. 16 G proteins act as middlemen or relays between extracellular first messengers and intracellular second messengers that cause responses within the cell. Slide 2 Ligand (1 st Receptor G protein Enzyme messenger) 2 nd messenger 1 Ligand* (1 st messenger) binds to the receptor. The receptor changes shape and activates. Extracellular fluid Ligand Receptor * Ligands include hormones and neurotransmitters. © 2013 Pearson Education, Inc. Intracellular fluid

Figure 3. 16 G proteins act as middlemen or relays between extracellular first messengers and intracellular second messengers that cause responses within the cell. Slide 3 Ligand (1 st Receptor G protein Enzyme messenger) 1 Ligand* (1 st messenger) binds to the receptor. The receptor changes shape and activates. Ligand 2 The activated receptor binds to a G protein and activates it. The G protein changes shape (turns “on”), causing it to release GDP and bind GTP (an energy source). 2 nd messenger Extracellular fluid Receptor G protein GDP * Ligands include hormones and neurotransmitters. © 2013 Pearson Education, Inc. Intracellular fluid

Figure 3. 16 G proteins act as middlemen or relays between extracellular first messengers and intracellular second messengers that cause responses within the cell. Slide 4 Ligand (1 st Receptor G protein Enzyme messenger) 1 Ligand* (1 st messenger) binds to the receptor. The receptor changes shape and activates. 2 The activated receptor binds to a G protein and activates it. The G protein changes shape (turns “on”), causing it to release GDP and bind GTP (an energy source). 2 nd messenger 3 Activated G protein activates (or inactivates) an effector protein by causing its shape to change. Extracellular fluid Effector protein (e. g. , an enzyme) Ligand Receptor G protein GDP * Ligands include hormones and neurotransmitters. © 2013 Pearson Education, Inc. Intracellular fluid

Figure 3. 16 G proteins act as middlemen or relays between extracellular first messengers and intracellular second messengers that cause responses within the cell. Slide 5 Ligand (1 st Receptor G protein Enzyme messenger) 1 Ligand* (1 st messenger) binds to the receptor. The receptor changes shape and activates. 2 The activated receptor binds to a G protein and activates it. The G protein changes shape (turns “on”), causing it to release GDP and bind GTP (an energy source). 2 nd messenger 3 Activated G protein activates (or inactivates) an effector protein by causing its shape to change. Extracellular fluid Effector protein (e. g. , an enzyme) Ligand Receptor G protein GDP * Ligands include hormones and neurotransmitters. © 2013 Pearson Education, Inc. Inactive 2 nd messenger Active 2 nd messenger 4 Activated effector enzymes catalyze reactions that produce 2 nd messengers in the cell. (Common 2 nd messengers include cyclic AMP and Ca 2+. ) Intracellular fluid

Figure 3. 16 G proteins act as middlemen or relays between extracellular first messengers and intracellular second messengers that cause responses within the cell. Slide 6 Ligand (1 st Receptor G protein Enzyme messenger) 1 Ligand* (1 st messenger) binds to the receptor. The receptor changes shape and activates. 2 The activated receptor binds to a G protein and activates it. The G protein changes shape (turns “on”), causing it to release GDP and bind GTP (an energy source). 2 nd messenger 3 Activated G protein activates (or inactivates) an effector protein by causing its shape to change. Extracellular fluid Effector protein (e. g. , an enzyme) Ligand Receptor G protein GDP Inactive 2 nd messenger Activated kinase enzymes * Ligands include hormones and neurotransmitters. © 2013 Pearson Education, Inc. 4 Activated effector enzymes catalyze reactions that produce 2 nd messengers in the cell. (Common 2 nd messengers include cyclic AMP and Ca 2+. ) 5 Second messengers activate other enzymes or ion channels. Cyclic AMP typically activates protein kinase enzymes. Intracellular fluid

Figure 3. 16 G proteins act as middlemen or relays between extracellular first messengers and intracellular second messengers that cause responses within the cell. Slide 7 Ligand (1 st Receptor G protein Enzyme messenger) 1 Ligand* (1 st messenger) binds to the receptor. The receptor changes shape and activates. 2 The activated receptor binds to a G protein and activates it. The G protein changes shape (turns “on”), causing it to release GDP and bind GTP (an energy source). 2 nd messenger 3 Activated G protein activates (or inactivates) an effector protein by causing its shape to change. Extracellular fluid Effector protein (e. g. , an enzyme) Ligand Receptor G protein GDP Inactive 2 nd messenger Activated kinase enzymes * Ligands include hormones and neurotransmitters. © 2013 Pearson Education, Inc. 4 Activated effector enzymes catalyze reactions that produce 2 nd messengers in the cell. (Common 2 nd messengers include cyclic AMP and Ca 2+. ) 5 Second messengers activate other enzymes or ion channels. Cyclic AMP typically activates protein kinase enzymes. 6 Kinase enzymes activate other enzymes. Kinase enzymes transfer phosphate groups from ATP to specific proteins and activate a Cascade of cellular responses series of other enzymes that trigger (The amplification effect is various metabolic and structural tremendous. Each enzyme changes in the cell. catalyzes hundreds of reactions. ) Intracellular fluid