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BU-101 / L16 · lecture

Membrane Composition

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BEFORE YOU START

You should understand the basic structure of a phospholipid molecule and recall that biological membranes are described as fluid mosaics.

Why this matters

Membrane composition dictates permeability, signalling capacity, and mechanical stability.

The specific ratio of lipids to proteins, and the types of lipids present, determine how a membrane functions in a given cellular context. A membrane rich in cholesterol is more rigid and less permeable to small molecules than one composed purely of phospholipids. Similarly, the presence of specific glycoproteins allows for cell-cell recognition, while ion channels require specific transmembrane proteins. Understanding composition is therefore essential for understanding how cells maintain homeostasis and communicate with their environment.

What makes up a membrane?

At its core, a biological membrane is a lipid bilayer. This structure is not a static wall but a dynamic assembly. The primary components are phospholipids, which form the bulk of the bilayer, and proteins, which are embedded within or attached to the surface. Cholesterol is also a major component in animal cell membranes, interspersed among the phospholipids. The exact proportions vary; for instance, the inner mitochondrial membrane is very protein-rich to support electron transport, whereas the myelin sheath is lipid-rich to provide electrical insulation. This variability allows membranes to be tailored to specific cellular needs, from structural support to active transport.

Lipid Diversity and Bilayer Properties

Phospholipids are the fundamental building blocks. Each molecule has a hydrophilic head and two hydrophobic tails. The nature of these tails significantly affects membrane fluidity. Saturated fatty acid tails are straight and pack tightly, increasing membrane rigidity. Unsaturated fatty acid tails contain kinks due to double bonds, preventing tight packing and increasing fluidity. The length of the acyl chains also matters; shorter chains interact less strongly, further enhancing fluidity. This fluidity is crucial for membrane processes such as endocytosis and the lateral movement of proteins.

Cholesterol acts as a buffer against temperature changes. At high temperatures, it restricts the movement of phospholipid tails, reducing fluidity. At low temperatures, it prevents the phospholipids from packing too closely, maintaining fluidity. This dual role ensures that membranes remain functional across a range of physiological conditions. The presence of cholesterol also reduces the permeability of the membrane to small water-soluble molecules, such as water and small polar solutes, by filling the spaces between the phospholipid tails.

Protein Integration and Function

Membrane proteins are classified based on their association with the lipid bilayer. Integral membrane proteins are embedded within the bilayer and often span it completely, known as transmembrane proteins. These proteins typically have hydrophobic regions that interact with the lipid tails and hydrophilic regions that extend into the aqueous environments on either side of the membrane. Peripheral membrane proteins are attached to the surface of the membrane, often interacting with the polar heads of phospholipids or with integral proteins. They can be removed relatively easily without disrupting the bilayer.

The function of membrane proteins is diverse. They serve as channels for the passive transport of ions and molecules, as pumps for active transport against concentration gradients, and as receptors for signal transduction. Enzymatic activity is also common, with proteins catalysing reactions at the membrane surface. The specific arrangement and density of these proteins determine the membrane's functional capabilities. For example, a high density of ion channels is found in nerve cell membranes to facilitate rapid electrical signalling, while a high density of transporters is found in intestinal epithelial cells for nutrient absorption.

Asymmetry and Dynamic Nature

Biological membranes are asymmetric. The composition of the lipid bilayer differs between the inner and outer leaflets. The outer leaflet typically contains more phosphatidylcholine and sphingomyelin, while the inner leaflet is enriched in phosphatidylethanolamine and phosphatidylserine. This asymmetry is maintained by specific enzymes, such as flippases, which move lipids between leaflets. The distribution of proteins is also asymmetric, with the sugar chains of glycoproteins and glycolipids facing almost exclusively the extracellular side. This asymmetry is critical for cell recognition, signalling, and the directionality of transport processes.

The membrane is not a static structure. Lipids and proteins can move laterally within the plane of the membrane, a process known as lateral diffusion. This movement is relatively fast, allowing components to mix and interact. However, movement between the two leaflets, known as flip-flop, is energetically unfavourable and occurs very slowly without the assistance of enzymes. This dynamic nature allows the membrane to respond to changes in the cellular environment and to facilitate processes such as vesicle fusion and fission.

The concept

◆ CONCEPT · T-004 · full treatment on its own page

The fluid mosaic membrane

A dynamic lipid bilayer studded with mobile proteins.

\[ \text{Membrane} = \text{fluid, self-assembled phospholipid bilayer} + \text{mosaic of embedded/associated proteins} \]
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Tier 3 ยท watch out

A common misconception is that the membrane is a uniform barrier. In reality, it is highly selective and asymmetric. The presence of cholesterol does not simply make the membrane "stiffer"; it modulates fluidity and permeability in a complex, temperature-dependent manner. Furthermore, the lipid composition is not static; it is actively regulated by the cell to meet its metabolic needs. C

Worked example

Problem. A synthetic lipid bilayer is composed of 50% phospholipids and 50% cholesterol by mass. If the average molecular mass of the phospholipids is \( 750\ \mathrm{g\,mol^{-1}} \) and the molecular mass of cholesterol is \( 386\ \mathrm{g\,mol^{-1}} \), calculate the molar ratio of phospholipids to cholesterol in the membrane.

  1. Determine the mass of each component in a \( 100\ \mathrm{g} \) sample of the membrane. Mass of phospholipids = \( 50\ \mathrm{g} \). Mass of cholesterol = \( 50\ \mathrm{g} \).
  2. Calculate the number of moles of each component. Moles of phospholipids = \( \frac{50\ \mathrm{g}}{750\ \mathrm{g\,mol^{-1}}} = 0.0667\ \mathrm{mol} \). Moles of cholesterol = \( \frac{50\ \mathrm{g}}{386\ \mathrm{g\,mol^{-1}}} = 0.1295\ \mathrm{mol} \).
  3. Calculate the molar ratio of phospholipids to cholesterol. Ratio = \( \frac{0.0667\ \mathrm{mol}}{0.1295\ \mathrm{mol}} \approx 0.515 \).
\[ \text{Molar Ratio (Phospholipid : Cholesterol)} \approx 0.52 : 1 \]

Units check. The ratio is dimensionless, as expected for a molar ratio.

CHECK YOURSELF

Three quick tests

  1. How does the presence of unsaturated fatty acids in phospholipid tails affect membrane fluidity?
    AnswerUnsaturated fatty acids introduce kinks in the tails, preventing tight packing and increasing membrane fluidity.
  2. What is the primary function of cholesterol in animal cell membranes?
    AnswerCholesterol modulates membrane fluidity and reduces permeability to small water-soluble molecules.
  3. Why is membrane asymmetry important for cell function?
    AnswerAsymmetry allows for specific cell recognition, signalling, and directional transport processes.
UNIT

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NOTES

Lecture notes drafted with a local model and checked line by line by the editor; every number in the worked example was recomputed.

Concepts cited: T-004 · Threads: structure, systems