W3 Membrane Structure and Function Flashcards

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1
Q

Describe the primary function of the CFTR protein in epithelial cells:

A

The CFTR (Cystic Fibrosis Transmembrane Conductance Regulator) protein functions as a chloride channel in epithelial cells. It allows chloride ions to move across the cell membrane, which is crucial for maintaining the balance of salt and water on epithelial surfaces, such as those in the lungs and sweat glands

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2
Q

What structural features are present in the CFTR protein?

A

The CFTR protein is characterized by:
Secondary Structures: It has 12 alpha helices that span the membrane

Functional Role: These helices form a channel through which chloride ions can pass.

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3
Q

Explain the impact of the defective CFTR protein on chloride ion transport and its consequences for patients with cystic fibrosis

A

In cystic fibrosis, the defective CFTR protein impairs chloride ion transport, leading to reduced secretion of chloride and sodium. This disruption causes thick, sticky mucus to accumulate in organs such as the lungs and pancreas, leading to respiratory infections, inflammation, and digestive issues

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4
Q

What are the main mutations associated with cystic fibrosis, and how do they affect the CFTR protein’s function?

A

There are over 2000 mutations in the CFTR gene, with the most common being the delta-F508 mutation. This mutation results in the deletion of a phenylalanine residue at position 508, causing improper folding of the CFTR protein. The misfolded protein is not properly transported to the cell surface, leading to defective chloride ion channel activity

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5
Q

What is the significance of the delta-F508 mutation in CF patients?

A

The delta-F508 mutation is the most prevalent mutation in cystic fibrosis, present in approximately 70% of CF patients. It leads to a defective CFTR protein that fails to reach the cell membrane, resulting in a significant reduction in chloride transport and the characteristic symptoms of cystic fibrosis

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6
Q

How do the treatments Trikafta / Kaftrio work to manage cystic fibrosis?

A

Trikafta (also known as Kaftrio) contains two correctors (elexacaftor and tezacaftor) and one potentiator (ivacaftor).

Correctors: These compounds help the CFTR protein fold properly and reach the cell surface.

Potentiators: They bind to the CFTR protein and increase the channel’s ability to open and allow chloride ions to pass through, improving chloride transport.

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7
Q

What is the difference between saturated and unsaturated fatty acids in terms of membrane fluidity?

A

Saturated fatty acids have no double bonds and are straight, leading to tighter packing and reduced membrane fluidity. Unsaturated fatty acids have one or more double bonds, creating kinks that prevent tight packing, thereby increasing membrane fluidity

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7
Q

What are the 3 key components of the plasma membrane, and what roles do they play?

A

The plasma membrane is composed of:

  1. Phospholipids: Form the lipid bilayer, providing a semi-permeable barrier.
  2. Proteins: Embedded in or associated with the membrane, facilitating various functions such as transport, signaling, and structural support.
  3. Carbohydrates: Attached to proteins (glycoproteins) and lipids (glycolipids), involved in cell recognition and protection
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8
Q

Explain the fluid mosaic model of membrane structure:

A

The fluid mosaic model describes the plasma membrane as a dynamic and flexible structure with a fluid lipid bilayer in which proteins are embedded and can move laterally. This model emphasizes the diversity of membrane proteins and the fluid nature of the lipid bilayer, allowing proteins and lipids to diffuse freely within the membrane

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9
Q

How does cholesterol affect membrane fluidity?

A

Cholesterol stabilizes the membrane by filling the gaps between phospholipids. At high temperatures, it reduces fluidity by making the membrane less permeable. At low temperatures, it prevents the membrane from becoming too solid by disrupting the packing of phospholipids.

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10
Q

Differentiate between peripheral and integral membrane proteins

A

Peripheral Proteins: These are attached to the membrane surface and interact with membrane lipids or other proteins. They do not penetrate the lipid bilayer

Integral Proteins: These span the entire lipid bilayer (transmembrane) and have hydrophobic regions that interact with the interior of the membrane, as well as hydrophilic regions that interact with the aqueous environments inside and outside the cell

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11
Q

Describe the function and significance of membrane carbohydrates, including glycolipids and glycoproteins

A

Membrane carbohydrates, found as glycolipids and glycoproteins, are involved in cell recognition, adhesion, and protection. They form the glycocalyx, which helps protect the cell surface and participate in cell-cell interactions.

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12
Q

What is passive transport, and how does it differ from active transport?

A

Passive transport is the movement of ions or molecules across a membrane down their concentration gradient without the need for energy. Active transport requires energy (usually from ATP) to move ions or molecules against their concentration gradient

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13
Q

Explain the roles of channel proteins and carrier proteins in membrane transport:

A

Channel Proteins: Form pores in the membrane that allow specific ions or molecules to pass through by diffusion. They are typically selective for particular substances

Carrier Proteins: Bind to specific molecules and undergo conformational changes to transport the molecules across the membrane. They can be involved in both facilitated diffusion and active transport

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14
Q

Define and distinguish between uniporters, symporters, and antiporters:

A
  1. Uniporters: Transport a single type of molecule in one direction (e.g., glucose transporter).
  2. Symporters: Transport two or more types of molecules simultaneously in the same direction (e.g., sodium-glucose symporter).
  3. Antiporters: Transport two or more types of molecules simultaneously in opposite directions (e.g., sodium-potassium pump)
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15
Q

Describe the process of osmosis and its effect on cells in hypotonic, isotonic, and hypertonic solutions:

A

Osmosis is the movement of water across a semipermeable membrane from an area of low solute concentration to an area of high solute concentration

Hypotonic Solution: Water flows into the cell, causing it to swell and potentially burst

Isotonic Solution: No net movement of water; the cell remains stable

Hypertonic Solution: Water flows out of the cell, causing it to shrink or shrivel

16
Q

What is primary vs. secondary active transport?

A
  1. Primary Active Transport: Direct use of ATP to move ions or molecules against their concentration gradient (e.g., sodium-potassium pump)
  2. Secondary Active Transport: Uses the energy from the electrochemical gradient created by primary active transport to move other substances against their concentration gradient (e.g., sodium-glucose symporter).
17
Q

What is Fluorescence Recovery after Photobleaching (FRAP), and how is it used to study membrane protein dynamics?

A

FRAP is a technique used to study the movement of proteins within the cell membrane. A fluorescently labeled region of the membrane is bleached with a laser, and the recovery of fluorescence in that region is monitored over time. This recovery indicates the diffusion of unbleached fluorescent proteins into the area, revealing information about protein mobility and membrane dynamics.

18
Q

What are the 6 main functions of the cell membrane? T - E - S - C- I - A

A

Transport: Facilitate the movement of ions and molecules across the membrane

Enzyme Activation: Catalyze biochemical reactions at the membrane

Signal Transduction: Receive and transmit signals from the environment to the cell’s interior

Cell Recognition: Help cells identify and interact with each other

Intercellular Joining: Facilitate connections between adjacent cells

Attachment to ECM: Anchor the cell to the extracellular matrix, providing structural support

18
Q

Outline the historical milestones in the discovery of cystic fibrosis

A

1938: Cystic fibrosis was first described as a distinct disease

1953: High levels of sodium and chloride in sweat were identified as a diagnostic marker for CF

1960s: Public health campaigns like “kiss your baby” promoted early detection of CF

1980s: CF was linked to a defective chloride channel, leading to an understanding of its pathophysiology

1989: The CFTR gene was identified, leading to the discovery of its role in cystic fibrosis and paving the way for targeted treatments