describe the arrangement of cholesterol, glycolipids and glycoproteins in cell surface membranes

Fluid‑Mosaic Model of the Plasma Membrane (Cambridge AS & A‑Level 9700 – Topic 4.1)

1. The phospholipid bilayer

  • Basic structure: two sheets of phospholipids. Each molecule has a

    • hydrophilic head‑group (e.g. phosphatidylcholine, phosphatidylethanolamine, phosphatidylserine) that faces the aqueous environments (extracellular fluid and cytosol)
    • two non‑polar fatty‑acid tails that form the interior hydrophobic core.

  • Bilayer asymmetry: the composition of the inner and outer leaflets differs.

    • Outer leaflet – rich in phosphatidylcholine, sphingomyelin and glycolipids.
    • Inner leaflet – enriched in phosphatidylethanolamine, phosphatidylserine and phosphatidylinositol.

  • Lateral mobility: phospholipids and most membrane proteins can move sideways, giving the membrane its fluid character.

2. Major surface‑membrane components and their arrangement

2.1 Cholesterol

  • Location: intercalated throughout both leaflets of the bilayer; the rigid sterol ring lies parallel to the fatty‑acid tails.
  • Examples: cholesterol (animal cells), ergosterol (fungi).
  • Functional roles (mapped to syllabus):

    • Stability – the rigid ring provides structural support.
    • Fluidity – buffers membrane fluidity; restricts movement at high temperature, prevents tight packing at low temperature.
    • Permeability – reduces passive diffusion of small water‑soluble molecules.
    • Signalling & transport – concentrates in lipid‑raft micro‑domains, helping to organise receptors and transport proteins.

2.2 Sphingolipids (including glycolipids)

  • Location: almost exclusively in the outer leaflet; the long saturated sphingosine backbone anchors the molecule in the bilayer.
  • Types:

    • Glycolipids – sphingolipid backbone + covalently attached carbohydrate chain (e.g. cerebrosides, gangliosides).
    • Sphingomyelin – phosphocholine head‑group, no carbohydrate.

  • Functional roles (mapped to syllabus):

    • Recognition – carbohydrate chains form the “sugar coat” that mediates cell‑cell recognition (blood‑group antigens, pathogen binding).
    • Protection – shields the membrane from mechanical damage and enzymatic attack.
    • Stability & fluidity – saturated sphingosine tails pack tightly, contributing to membrane order.
    • Signalling & transport – together with cholesterol they create lipid‑raft micro‑domains that concentrate receptors, ion channels and transporters.

2.3 Glycoproteins

  • Location:

    • Integral (transmembrane) glycoproteins – span the bilayer via one or more α‑helical segments.
    • Peripheral glycoproteins – attached to the membrane surface by lipid anchors (e.g. GPI‑anchor) or by non‑covalent interactions with integral proteins.

  • Carbohydrate attachment:

    • N‑linked (to asparagine) – added in the endoplasmic reticulum.
    • O‑linked (to serine/threonine) – added in the Golgi apparatus.

  • Functional roles (mapped to syllabus):

    • Recognition – extracellular carbohydrate chains act as specific binding sites for hormones, antibodies, lectins.
    • Signalling – receptor glycoproteins bind ligands and trigger intracellular cascades (e.g. insulin receptor, GPCRs).
    • Transport – carrier glycoproteins undergo conformational changes to move solutes across the membrane (e.g. GLUT1, Na⁺/K⁺‑ATPase).
    • Channel activity – form pores that allow rapid passage of ions or water (e.g. voltage‑gated Na⁺ channels, aquaporins).
    • Adhesion – adhesion glycoproteins mediate cell‑cell or cell‑matrix contacts (e.g. integrins, selectins).
    • Stability & fluidity – interactions with the cytoskeleton and with cholesterol help maintain membrane integrity.

3. Lipid‑raft micro‑domains

  • Enriched in cholesterol and sphingolipids (including glycolipids).
  • Form relatively ordered, less‑fluid patches that compartmentalise membrane proteins such as receptors, ion channels and transporters.
  • Play a key role in signal transduction, endocytosis and pathogen entry – all mentioned in the syllabus under “cell‑surface receptors”.

4. Summary table – component, location & syllabus‑linked functions

ComponentLocation in membraneSyllabus‑linked functional roles
CholesterolIntercalated evenly in both leafletsStability, fluidity (temperature buffer), permeability, contributes to lipid‑raft signalling/transport
Sphingolipids (glycolipids & sphingomyelin)Predominantly outer leafletRecognition (sugar coat), protection, stability & fluidity (tight packing), lipid‑raft formation for signalling & transport
Glycoproteins (integral + peripheral)Spanning the bilayer or surface‑attached via lipid anchorsRecognition, signalling, transport (carriers), channel activity, adhesion, stability & fluidity (cytoskeletal links)

5. Key points to remember (exam‑style checklist)

  • The membrane is a dynamic fluid‑mosaic of phospholipids, cholesterol, sphingolipids and proteins.
  • Phospholipid heads are polar (phosphate‑choline, phosphate‑ethanolamine, etc.) and the two leaflets are asymmetric in composition.
  • Cholesterol is present in both leaflets, modulating fluidity, stability and permeability.
  • Sphingolipids/glycolipids are restricted to the outer leaflet; their carbohydrate chains form the extracellular sugar coat and participate in cell‑cell recognition.
  • Glycoproteins may be integral or peripheral; they perform the five major membrane functions required by the syllabus:

    1. Stability
    2. Fluidity
    3. Permeability
    4. Transport (carriers & channels)
    5. Signalling & recognition (receptors, adhesion molecules)

  • Lipid rafts are cholesterol‑ and sphingolipid‑rich micro‑domains that organise receptors and transport proteins for efficient signalling.

Suggested diagram: Cross‑section of a fluid‑mosaic membrane showing (i) phospholipid bilayer with distinct head‑group polarity, (ii) cholesterol interspersed in both leaflets, (iii) sphingolipid/glycolipid molecules confined to the outer leaflet, (iv) transmembrane glycoproteins with extracellular carbohydrate chains, and (v) a lipid‑raft patch enriched in cholesterol and sphingolipids.