Signal Transduction, ECM, Mitochondria (Lecture 17) Flashcards

1
Q

What do integral membrane proteins have?

Molecules move across membranes through what mechanisms?

Ion channels are what?

Tetrodotoxin and Curare are what?

What is the Na+ glucose symporter?

How do active transporters move molecules from lower to higher concentrations?

A
  • Integral membrane proteins have transmembrane domains (𝛼 helices) made of hydrophobic amino acids
  • Molecules move across membranes through passive and active mechanisms
  • Ion channels are gated and can be activated by voltage (charge) or ligands
  • Tetrodotoxin and Curare are toxins that interfere with movement through ion channels
  • The Na+ glucose symporter uses the higher concentration of Na+ to drive glucose against a concentration gradient
  • Active Transporters use energy (ATP) to move molecules from lower to higher concentrations
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2
Q

Integral Membrane proteins ( Transmembrane proteins) have many important roles in cell function

What type of transmembrane proteins has been discussed thus far?

A
  • ACh nicotinic receptor (ligand-gated channel)
  • Na+ channels Glucose transporter Na+-glucose symporter
  • Na+/K+ ATPase pump
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3
Q

What are membrane proteins important for?

How do signals from outside the cell get “into” the cell?

A
  • Membrane proteins are important for signal transduction
  • How do signals from outside the cell get “into” the cell?
    • Ligand (a small molecule that binds to a receptor)
    • Ligand binding changes the conformation of the receptor protein
      • (Note: the ligand does not enter the cell)
    • The cytosolic side of the receptor protein is affected by the conformation change
    • These conformational changes cause other proteins (in the cytosol or membrane-bound) to become activated
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4
Q

How epinephrine activates the conversion of glycogen to glucose is an example of what?

A

How epinephrine activates the conversion of glycogen to glucose is an example of a signal transduction

Epinephrine is made in adrenal glands (FLight or fight response/acute stress response) → Blood → Liver

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5
Q

How epinephrine activates the conversion of glycogen to glucose is an example of a signal transduction

How is epinephrine (adrenalin) made?

A

epinephrine (adrenalin) is made in the adrenal gland → blood → liver

epinephrine (Ligand) → binds to a receptor on liver cell → conformation change on the cytosolic side

When the G-protein is “off” it has GDP, the GDP gets converted to GTP and the G-protein is now “on”, this signal cascade breaks down glycogen to glucose

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6
Q

Why are membrane proteins important?

What are multicellular organisms composed of?

What does ECM =?

A
  • Membrane proteins are important for interacting with components in the extracellular matrix (ECM)
  • Multicellular organisms are composed of tissues and organs consisting of communities of cells. These cells work together to perform a function; e.g., skin, liver, leaves, etc.
  • ECM = organized network of material produced and secreted by cells
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7
Q

What cells have walls?

Plant cell walls = ECM

Are composed of…

Provide…

Protect…

A
  • Cells of bacteria, plants, and fungi have walls
  • Plant cell walls = ECM
  • composed of cellulose, hemicellulose, pectin, and proteins
  • provide structural support to the cell and to the whole organism (‘skeleton’)
  • protect the cell from mechanical damage and pathogen attack
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8
Q

What are the main functions of these intracellular compartments?

Cytosol

Nucleus

Endoplasmic Reticulum

Golgi apparatus

Lysosomes

Endosomes

Mitochondria

Chloroplasts

Peroxisomes

A

Cytosol - Protein synthesis, many metabolic pathways

Nucleus - Contains genome, DNA, RNA synthesis, ribosome assembly

Endoplasmic Reticulum - Synthesis of lipids, synthesis of proteins

Golgi Apparatus - Protein modification, packaging of proteins and lipids

Lysosomes - Degradation of cellular material

Endosomes - Sorting, recycling

Mitochondria - ATP synthesis, apoptosis

Chloroplasts - Photosynthesis, ATP synthesis

Peroxisomes - Oxidation of toxic molecules

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9
Q

Origin of the Eukaryotic Cells:

What is the Endosymbiont Theory?

A

Theory: Double-membraned organelles present in eukaryotic cells (i.e., mitochondria & chloroplasts) are derived from formerly free-living prokaryotes that were engulfed by an ancestral cell for endosymbiosis

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10
Q

What is the respiration equation?

A

(CH2O) + O2 → CO2 + H2O + ATP

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11
Q

What is the photosynthesis equation?

A

CO2 + H2O →sunlight→ (CH2O) + O2

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12
Q

Mitochondria: Structure and Function?

A

Mitochondria have a double membrane, consisting of an inner and outer membrane and an aqueous compartment in between

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13
Q

Mitochondria have two membranes: What is the first?

A
  1. Outer Mitochondrial Membrane (OMM)
    * contains many enzymes with diverse metabolic functions
    * Porins
    • large channels
    • when open, the membrane is freely permeable (e.g. to ATP)
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14
Q

Mitochondria have two membranes: What is the second?

A
  1. Inner Mitochondrial Membrane (IMM)
  • high protein: lipid ratio (3:1)
  • double-layered folds = cristae
  • cristae:
    • increase the membrane surface area
    • contain machinery for aerobic respiration and ATP formation
  • rich in a phospholipid called cardiolipin (characteristic of bacterial membranes)
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15
Q

Aqueous compartments of mitochondria

What are the two compartments?

A

1. intermembrane space

2. matrix

  • high [protein] - gel-like consistency
  • mitochondrial ribosomes
  • mitochondrial DNA (mtDNA)
    • encodes polypeptides that are integrated into the IMM, ribosomes, tRNA
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16
Q

Oxidative Phosphorylation:

ATP Synthesis in the Mitochondria

What are the two steps in brief?

A

ATP Synthesis in the Mitochondria

Step 1

  • electron transport and proton pumping
    • generates an electrochemical gradient

Step 2

  • proton (H+) movement down electrochemical gradient powers ATP synthesis
17
Q

Oxidative Phosphorylation: Explain step 1

A

Oxidative Phosphorylation: Step 1

  • high-energy electrons (e-) pass from coenzymes (NADH and FADH2) in the matrix to electron carriers in IMM
  • series of e- carriers
    • (respiratory enzyme complexes I, II, III, IV)
    • = electron-transport chain (ETC)
  • energy transfer at each complex used to pump protons (H+) from the matrix into intermembrane space
  • ultimately, low energy e- is transferred to a terminal e- acceptor (O2)
    • H2O produced
18
Q

Oxidative Phosphorylation: Explain step 2

A
  • Controlled movement of protons back across IMM
  • via ATP synthase
  • the potential energy in an electrochemical gradient across IMM converted to ATP in the matrix