why is patrick paralyzed?
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Why is Patrick Paralyzed?. Maureen Knabb Department of Biology West Chester University. Patrick at 2:. Patrick at 21: Movie in QuickTime ( mov ). Why did Patrick lose his ability to move?. Patrick’s History. - PowerPoint PPT PresentationTRANSCRIPT
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Why is Patrick Paralyzed?
Maureen KnabbDepartment of Biology
West Chester University
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Why did Patrick lose his ability to move?
Patrick at 2: Patrick at 21:Movie in QuickTime (mov)
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Patrick’s History• When Patrick was 16 years old, his hand started
twitching as he picked up a glass at dinner.• Five months later (in February 2001), he fell down
the steps at his home and was unable to climb the steps to the bus. He went to the ER for his progressive weakness.
• At Children’s Hospital of Philadelphia he was initially diagnosed with a demyelinating disease.
• He was treated with anti-inflammatory drugs and antibodies for 2 years with no improvement.
• What was wrong with Patrick?
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CQ1: What could be responsible for Patrick’s loss of mobility?
A: His nervous system is not functioning properly.
B: His muscles are not functioning properly.
C: He cannot efficiently break down food for energy.
D: All of the above are possible causes.
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CQ2: Which of the following processes requires energy?
A: Creating ion gradients across membranes.
B: Muscle relaxation.
C: Protein synthesis.
D: All of the above.
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Why do nerve and muscle cells need energy?
• Synthetic work = building macromolecules – (e.g., Making protein)
• Mechanical work = moving molecules past each other– (e.g., Muscle relaxation)
• Concentration work = creating chemical gradients – (e.g., Storing glucose)
• Electrical work = creating ion gradients – (e.g., Unequal distribution of sodium and potassium ions)
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What is energy?• Potential Energy = stored energy
– Chemical bonds– Concentration gradients– Electrical potential
• Kinetic Energy = movement energy– Heat = molecular motion– Mechanical = moving molecules past each other– Electrical = moving charged particles
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Cycling between stored chemical versus movement energy
• Stored chemical energy must be released– Processes that RELEASE energy
• Make ATP• Catabolic/ Exergonic
• Movement requires energy– Processes that REQUIRE energy
• Use ATP• Anabolic/ Endergonic
• Energy released > Energy required• ATP plays a central role
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ATP plays a central role in energy cycling
+Stored
chemical energy is
released in catabolic
reactions tomake ATP
ATP is used in energy requiring
reactions like muscle
movement
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CQ3: The high energy phosphate bond in ATP is _____ and ____ energy to break the bond.
A: Easy to break, releasesB: Hard to break, requiresC: Easy to break, requiresD: Hard to break, releases
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Adenosine triphosphate (ATP)
This bond is easy to break and releases energy!
Hydrolysisof ATP
H2O
Formation of these new bonds Requires energy
Adenosine diphosphate (ADP)Inorganicphosphate (Pi)
H H
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ATP plays a central role in metabolism
• ATP is NOT the highest energy molecule– intermediate energy
• ATP hydrolysis releases energy overall– phosphate groups require low energy to break– new bonds formed release more energy than
the energy required to break the bond• Phosphorylation by ATP increases the
energy of other molecules
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CQ4: What would happen if Patrick lost his ability to make ATP?
A: His muscles would not be able to contract.
B: His neurons would not be able to conduct electrical signals.
C: Both A and B.
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How is ATP generated?
• ATP is formed through metabolic pathways.
• In metabolic pathways, the product of one reaction is a reactant for the next.
• Each reaction is catalyzed by an enzyme.
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What are enzymes?
• Enzymes (usually proteins) are biological catalysts, highly specific for their substrates (reactants).
• Enzymes change reactants into products through transition state intermediates.
• Enzymes are not consumed in the reaction.
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Enzymes as Catalysts
• Enzymes “speed up” reactions by lowering the “activation energy” of a reaction.
• Enzymes DO NOT change the overall energy released in a reaction.
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CQ5: Which statement about enzymes is correct?
A: Enzymes are always proteins. B: Enzymes are consumed in a reaction. C: Enzymes are always active.D: All are correct.E: None are correct.
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Enzyme Regulation• Enzymes turn “on” and “off” based on the
need of the organism– “ON” = Activators
• Positive allosteric regulation
– “OFF” = Inhibitors• Irreversible = must make new enzyme!• Reversible = inhibitor can “come off”
– Competitive = active site– Noncompetitive = “other” site = allosteric site
• Feedback Inhibition
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CQ6: In competitive inhibition…A: the inhibitor competes with the normal
substrate for binding to the enzyme's active site.
B: an inhibitor permanently inactivates the enzyme by combining with one of its functional groups.
C: the inhibitor binds with the enzyme at a site other than the active site.
D: the competing molecule's shape does not resemble the shape of the substrate molecule.
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How are metabolic pathways regulated?
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Feedback inhibition animation
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DNA mutations can disrupt metabolic pathways
• Patrick suffered from a genetic disease that altered the structure of one protein.
• The protein was an enzyme.• The enzyme could potentially:
• lose its ability to catalyze a reaction.• lose its ability to be regulated.
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CQ7: Consider the following metabolic pathway:A C D
BIf the enzyme responsible for converting A to C was
mutated and nonfunctional, what would happen?
A: A levels would increase; B, C, and D levels would decrease.
B: A and B levels would increase; C and D levels would decrease.
C: A, B and C levels would increase; D levels would decrease.
D: A, B, C, and D levels would all decrease.
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Metabolic Pathways: Glycolysis
• Pathway present in almost every cell!• Takes place in the cytoplasm of the cell.• Occurs with or without oxygen.• Oxidizes glucose (6 C) to 2 pyruvate (3 C).• Overall yield = 2 ATP and 2 NADH + H+
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Important Electron AcceptorsCoenzymes
• NAD (Nicotinamide Adenine Dinucleotide)– NAD+ + 2H+ + 2 e- --> NADH+ + H+
• FAD (Flavin Adenine Dinucleotide)– FAD + 2H+ + 2 e- --> FADH2
• Both molecules serve as coenzymes in many reactions.
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Fermentation: Recycles NADH
• Occurs in the cytoplasm without O2
• NADH + H+ is reoxidized to NAD+
• Alcoholic Fermentation = yeast cells– Converts pyruvate to ethanol and CO2
– Overall yield = 2 ATP• Lactate Fermentation = animal cells
– Converts pyruvate to lactate– Overall yield = 2 ATP
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CQ8: Consider the following metabolic pathway: Pyruvate Acetyl CoA TCA cycle LactateIf Patrick’s enzyme responsible for converting pyruvate to acetyl CoA was inhibited, what would happen?
A: Pyruvate levels would increase; acetyl CoA and lactate levels would decrease.
B: Pyruvate and lactate levels would increase; acetyl CoA levels would decrease.
C: Pyruvate, acetyl CoA, and lactate levels would increase.
D: Pyruvate, acetyl CoA, and lactate levels would all decrease. 26
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Patrick suffered from lactate acidosis
• Lactate (lactic acid) and pyruvate accumulated in his blood.
• Acidosis led to:– Hyperventilation– Muscle pain and weakness– Abdominal pain and nausea
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Mitochondria
Cell membrane
Outer membrane
Intermembrane space
Inner membranematrix
cytoplasm
GlucoseNa+
Glucose2 ATP
2 NADH + H+
2 Pyruvate
No O2 2 Lactate (fermentation)Glycolysis
With O2
Pyruvate
Acetyl CoA
3 NADH +H+ FADH2
GTP
ATP
2 CO2
NADH +H+
NAD+
3 NAD+
Electron transport carriers
F0F1
ATPase
CO2CO2 diffuses out
of the cell
Oxaloacetate
citrateGDP + Pi
FAD
H+
H+
H+H+
e-
e-e-
e-e-
H+
H+
ADP + Pi
ATP
O2
Oxygen diffuses into the cell
H2O
O2
Krebs cycle
Anaerobic versus aerobic metabolism
Pyruvate dehydrogenase
enzyme
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What happened to Patrick?• He inherited a mutation
leading to a disease called pyruvate dehydrogenase complex disease (PDCD).
• Pyruvate dehydrogenase is an enzyme that converts pyruvate to acetyl CoA inside the mitochondria.
• The brain depends on glucose as a fuel. PDCD degenerates gray matter in the brain.
• Pyruvate accumulates, leading to alanine and lactate accumulation in the blood (lactate acidosis). 29
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CQ9: Why did Patrick become paralyzed?A: He inherited a genetic disease that resulted in the
partial loss of an enzyme necessary for aerobic breakdown of glucose.
B: The enzyme that is necessary for metabolizing fats was defective.
C: He was unable to synthesize muscle proteins due to defective ribosomes.
D: He suffered from a severe ion imbalance due to a high salt diet.
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CQ10: Which food(s) can be metabolized to generate acetyl CoA?
A: Carbohydrates
B: Fats
C: Proteins
D: Both carbohydrates and fats
E: Carbohydrates, fats and proteins
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Are there any treatment options for PDH deficiency?
• High fat, low carbohydrate diet (ketogenic diet)
• Fatty acids can form acetyl CoA which can enter the Krebs cycle
Fatty acids
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Are there any treatment options for PDH deficiency?
• Dichloroacetate (DCA) blocks the enzyme that converts PDH from active to inactive forms
• PDH remains in the active form
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DCA blocks here
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CQ11: Dichloroacetate (DCA) administration would lead to…
A: Increased production of acetyl CoA.B: Decreased lactate accumulation.C: Increased ATP production.D: All of the above.
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CQ12: The loss of which of the following molecules was the most critical for Patrick’s paralysis?
A: Pyruvate dehydrogenaseB: Acetyl CoAC: LactateD: ATP
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What happened to Patrick?
• Although his family tried to care for him at home, Patrick remained in hospitals and nursing homes until he died in 2006.
• Patrick died due to pneumonia, sepsis, and renal failure when he was only 21 years old.
• His family mourns his loss but feels grateful that he was able to survive for 5 years on a respirator, 4 years beyond his doctor’s predictions.
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