Ch 11: Biological Membranes and Transport: Structure, Dynamics, and Function

Biological Membranes and Transport

Introduction

Biological membranes are essential components of all living cells, providing structural integrity, compartmentalization, and regulation of molecular traffic. This chapter explores the composition, architecture, dynamics, and transport mechanisms associated with biological membranes.

The Composition and Architecture of Membranes

Lipid Aggregates: Micelles, Bilayers, and Vesicles

Membrane lipids are amphipathic molecules that spontaneously form organized structures in aqueous environments due to hydrophobic interactions. The three principal types of lipid aggregates are micelles, bilayers, and vesicles.

• Micelles: Spherical structures formed by amphipathic molecules with hydrophobic tails inward and hydrophilic heads outward. Favored when the head group is larger than the acyl chain cross-section.

• Bilayers: Two lipid monolayers (leaflets) form a two-dimensional sheet. Favored when the head group and acyl chain cross-sections are similar.

• Vesicles (Liposomes): Spherical bilayers enclosing an aqueous cavity, formed when a bilayer sheet folds back on itself.

Fluid Mosaic Model and Membrane Function

The fluid mosaic model describes membranes as dynamic structures with proteins and lipids capable of lateral movement. This architecture allows for selective permeability, cell signaling, and adaptability to environmental changes.

• Membranes permit shape changes, exocytosis, endocytosis, and cell division.

• Proteins serve as transporters, receptors, ion channels, and adhesion molecules.

Endomembrane System and Membrane Trafficking

The endomembrane system includes organelles surrounded by single or double membranes, such as the ER, Golgi apparatus, lysosomes, nucleus, mitochondria, and chloroplasts. Membrane trafficking involves the movement and modification of lipids and proteins between these compartments.

Membrane Lipid Asymmetry

Lipids are asymmetrically distributed between the two leaflets of the plasma membrane, with sphingolipids and cholesterol often replacing phosphatidylcholine in the outer leaflet during trafficking.

Membrane Proteins: Types and Topology

Classification of Membrane Proteins

• Integral membrane proteins: Firmly embedded within the lipid bilayer, often spanning the membrane.

• Peripheral membrane proteins: Associate with the membrane via electrostatic interactions and hydrogen bonds.

• Amphitropic proteins: Reversibly associate with membranes, found in both membranes and cytosol.

• Monotopic proteins: Interact with only one leaflet of the membrane.

• Bitopic proteins: Span the bilayer once with a single hydrophobic sequence.

• Polytopic proteins: Cross the membrane multiple times, typically as α-helices.

Membrane Protein Topology and Prediction

Integral membrane protein topology can often be predicted from the amino acid sequence. An α-helical segment of 20–25 residues is sufficient to span the bilayer. Hydropathy plots are used to identify hydrophobic transmembrane segments.

β-Barrel Proteins and Amino Acid Distribution

Some membrane proteins form β-barrels, with alternating hydrophobic and hydrophilic residues. Aromatic residues (Tyr, Trp) often anchor proteins at the membrane interface, and positively charged residues (Lys, Arg) are more common on the cytoplasmic face (positive-inside rule).

Membrane Dynamics

Lipid Mobility and Membrane Fluidity

Lipids in membranes exhibit various types of motion, contributing to membrane fluidity:

• Liquid-ordered (Lo) state: Gel-like, with constrained motion.

• Liquid-disordered (Ld) state: High lateral and rotational mobility.

Lateral and Transverse Diffusion

Lipids can rotate and diffuse laterally within a leaflet rapidly. Transverse (flip-flop) diffusion is rare and slow but can be catalyzed by specific enzymes.

Experimental Measurement of Lipid Mobility

Fluorescence recovery after photobleaching (FRAP) is used to measure the rate of lateral diffusion of lipids and proteins in membranes.

Enzymatic Catalysis of Lipid Translocation

• Flippases: Move phosphatidylethanolamine (PE) and phosphatidylserine (PS) from the outer to the cytoplasmic leaflet (ATP-dependent).

• Floppases: Move phospholipids and sterols from the cytoplasmic to the outer leaflet (ATP-dependent).

• Scramblases: Move lipids in either direction toward equilibrium (not ATP-dependent; some require Ca2+).

Hop Diffusion and Membrane Microdomains

Lipid molecules diffuse laterally within small regions, with occasional 'hops' between regions. Microdomains (rafts) enriched in cholesterol and sphingolipids are thicker and more ordered, influencing protein localization and signaling.

Solute Transport Across Membranes

Types of Transport

• Simple diffusion: Nonpolar compounds cross membranes unassisted down their concentration gradient.

• Facilitated diffusion (passive transport): Polar compounds and ions require specific protein carriers to move down their gradient.

• Active transport: Movement against a concentration or electrochemical gradient, requiring energy input.

Membrane Potential and Electrochemical Gradient

The membrane potential (Vm) is the electrical gradient across a membrane, influencing ion movement. The electrochemical gradient combines chemical and electrical gradients to determine solute movement direction.

Transport Proteins: Transporters and Ion Channels

• Transporters: Bind solutes and undergo conformational changes to move them across membranes; can be passive or active.

• Ion channels: Provide aqueous pores for rapid ion movement; typically gated and selective, not saturable.

Passive Transport: Glucose Transporters

GLUT1 mediates passive glucose transport in erythrocytes, following Michaelis-Menten-like kinetics:

$V_0 = \frac{V_{max} [S]_{out}}{K_t + [S]_{out}}$

where $V_0$ is the initial velocity, $[S]_{out}$ is the external glucose concentration, and $K_t$ is the transport constant.

Active Transport: P-Type, V-Type, F-Type ATPases, and ABC Transporters

• P-type ATPases: Undergo phosphorylation during the transport cycle (e.g., Na+/K+ ATPase, Ca2+ ATPase).

• V-type ATPases: Acidify intracellular compartments by pumping protons.

• F-type ATPases (ATP synthases): Synthesize ATP using a proton gradient.

• ABC transporters: Use ATP hydrolysis to transport a wide variety of substrates, including drugs and lipids.

Secondary Active Transport

Secondary active transport couples the uphill movement of one solute to the downhill movement of another, such as the Na+-glucose symporter in intestinal cells.

Equations for Free-Energy Change in Transport

• Uncharged solute: $\Delta G_t = RT \ln \left( \frac{C_2}{C_1} \right)$

• Ion (charged solute): $\Delta G_t = RT \ln \left( \frac{C_2}{C_1} \right) + ZF \Delta \psi$ where $Z$ is the ion charge, $F$ is the Faraday constant, and $\Delta \psi$ is the membrane potential.

Aquaporins and Ion Channels

Aquaporins facilitate rapid water movement across membranes, while ion-selective channels allow specific ions to cross in response to voltage or ligand binding. These channels are critical for processes such as nerve impulse conduction and osmoregulation.

Summary Table: Major Membrane Transporters

Transporter Type	Energy Source	Direction	Example
Simple diffusion	None	Down gradient	O2, CO2
Facilitated diffusion	None	Down gradient	GLUT1 (glucose)
Primary active transport	ATP hydrolysis	Against gradient	Na+/K+ ATPase
Secondary active transport	Ion gradient	Against gradient	Na+-glucose symporter
Ion channel	None	Down gradient	K+ channel
Aquaporin	None	Down gradient	AQP1

Additional info: This summary integrates foundational concepts from the Lehninger Principles of Biochemistry and expands on the provided lecture content for comprehensive exam preparation.