BackExam 4- chap 11 Membrane
Study Guide - Smart Notes
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Membrane Structure and Architecture
Composition and Organization of Membranes
Biological membranes are essential for compartmentalization in cells, composed primarily of a lipid bilayer with embedded proteins. The amphipathic nature of phospholipids drives the formation of bilayers, which are stabilized by hydrophobic interactions.
Phospholipids have hydrophilic heads and hydrophobic tails, causing them to self-assemble into bilayers in aqueous environments.
Bilayer formation is energetically favorable due to the exclusion of water from hydrophobic tails.
Micelles vs. Bilayers: Bilayers are more stable for phospholipids due to their two hydrophobic tails, while micelles are favored by single-tailed lipids.
Example: The plasma membrane of eukaryotic cells is a classic example of a lipid bilayer with embedded proteins.
Membrane Functions
Major Roles of Membranes
Membranes perform a variety of functions essential for cellular life.
Compartmentalization of cellular processes
Regulation of transport (selective permeability)
Signal transduction and communication
Energy transduction (e.g., mitochondria, chloroplasts)
Cell recognition and adhesion
Membrane Proteins: Types and Functions
Classification of Membrane Proteins
Membrane proteins are classified based on their association with the lipid bilayer:
Type | Location | Function |
|---|---|---|
Integral | Span or are embedded in the bilayer | Transport, signaling, structural support |
Peripheral | Associated with membrane surface | Enzyme activity, signaling, cytoskeletal attachment |
Amphitropic | Reversibly associate with membrane | Regulation, signaling |
Integral proteins often contain transmembrane α-helices or β-barrels.
Peripheral proteins interact via non-covalent interactions and can be removed by salt or pH changes.
Amphitropic proteins associate with membranes in response to signals or modifications.
Example: Receptors, channels, and enzymes are common integral membrane proteins.
Membrane Fluidity
Factors Affecting Fluidity
Membrane fluidity is determined by lipid composition and temperature.
Unsaturated fatty acids increase fluidity due to kinks in their tails.
Saturated fatty acids decrease fluidity by allowing tight packing.
Cholesterol modulates fluidity by disrupting packing at low temperatures and restraining movement at high temperatures.
Example: Bacteria adjust fatty acid composition in response to temperature changes to maintain membrane fluidity.
Membrane Domains and Rafts
Lipid Rafts and Protein Targeting
Membranes are not uniform; specialized domains called lipid rafts are enriched in cholesterol and sphingolipids, serving as platforms for signaling and trafficking.
Rafts organize specific proteins for efficient signaling.
Targeting proteins to rafts can increase the efficiency of cellular processes.
Example: GPI-anchored proteins are often found in lipid rafts.
Membrane Fusion
Role in Cellular Processes
Membrane fusion is critical for processes such as vesicle trafficking, neurotransmitter release, and cell division.
Fusion involves proteins that mediate the merging of lipid bilayers.
SNARE proteins are key mediators of vesicle fusion in neurons.
Example: Neurotransmitter release at synapses requires membrane fusion.
Membrane Transport Mechanisms
Passive vs. Active Transport
Transport across membranes can be passive (no energy required) or active (energy required).
Passive transport includes simple diffusion and facilitated diffusion.
Active transport requires energy, often from ATP hydrolysis.
Equation for Free Energy Change in Transport:
and are concentrations on either side of the membrane.
is the charge, is Faraday's constant, is the membrane potential.
Types of Transporters
Channels: Allow rapid movement of ions or water (e.g., K+ channels).
Carriers: Bind and transport specific molecules (e.g., glucose transporter).
Pumps: Use energy to move substances against gradients (e.g., Na+/K+ ATPase).
Facilitated Diffusion
Facilitated diffusion uses transport proteins to move substances down their concentration gradients without energy input.
Binding energy lowers activation energy for transport.
Specificity arises from precise interactions between transporter and substrate.
Example: Glucose transport into cells via GLUT transporters.
Active Transport
Active transport moves substances against their gradients, requiring energy.
Primary active transport: Direct use of ATP (e.g., Na+/K+ ATPase).
Secondary active transport: Uses gradients established by primary transporters (e.g., symporters and antiporters).
ABC Transporters use ATP to export hydrophobic drugs and metabolites.
Ion Channels and Gated Transport
Voltage-Gated and Ligand-Gated Channels
Ion channels can be regulated by voltage changes or ligand binding.
Voltage-gated channels open in response to changes in membrane potential.
Ligand-gated channels open when specific molecules bind to the channel.
Example: Potassium channels open during action potentials in neurons.
Neurotransmitters and Channel Activation
Neurotransmitters can trigger ligand-gated ion channels, leading to rapid cellular responses.
Neurotransmitter | Receptor Type | Effect |
|---|---|---|
Acetylcholine | Nicotinic receptor | Opens Na+ channels |
GABA | GABAA receptor | Opens Cl- channels |
Glutamate | NMDA/AMPA receptor | Opens Ca2+/Na+ channels |
Additional info: | Other neurotransmitters (e.g., glycine, serotonin) also act via ligand-gated channels. |
Summary Table: Major Transporters in Epithelial Cells
Transporter | Location | Function |
|---|---|---|
Na+/K+ ATPase | Basolateral membrane | Pumps Na+ out, K+ in |
Glucose transporter (SGLT) | Apical membrane | Co-transports Na+ and glucose into cell |
ABC transporter | Various | Exports hydrophobic drugs/metabolites |
Additional info: | Other transporters include Cl- channels and antiporters for pH regulation. |
Key Equations and Concepts
Free energy change for transport:
Binding energy lowers activation energy for facilitated diffusion.
ATP hydrolysis provides energy for active transport.
Additional info:
Membrane trafficking, signaling, and disease mechanisms are closely linked to membrane structure and transport.
Disorders such as cystic fibrosis result from defects in membrane transport proteins.