Lipid bilayer
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Each cell in our human body is composed of a unit membrane which separates the cytoplasm from the outer / extracellular environment. The most important components of this membrane are the phospholipids and within them lecithin is the most common one. Membranes differ from 7.5 to 10 nm in thickness and appear as trilamellar structure in electron microscopes after fixation in osmium tetroxide. Because all membranes of cells and of cell organelles have this appearance, the 3-layered structure was designated the unit membrane, which is a phospholipid bilayer.

Lecithin and its structure

The most common phospholipid is lecithin (phosphatidylcholine) that consists of two non-polar (water-repelling) long-chain fatty acids linked to a charged polar (water-attracting) head group. Within the polar head the molecule of glycerol is esterified with two fatty acid molecules and one phosphate molecule which is esterified with aminoalcohol choline. A substance, that is both polar and non-polar, is termed amphipapthic. The most stable option is gained unter the following circumstances - outer leaf of the membrane: phosphatidylcholie, sphingomyelins, many molecules of cholesterol - inner leaf of the membrane: phosphatidylserine, phosphidylethanolamine, cephalin The inner and outer leaf molecules can form lipid rafts (lateral diffusion). A flip-flop is a swap of a phospholipid with the aid of flipases (enzymes).

Arrangements of phospholipids in water

Monolayer

Micelles

Bilayer (double membrane and liposom / vesicle)

The hydrophilic / lipophobic polar heads are directed towards each surface of the membrane, in direct contact with water. The hydrophobic / lipophilic nonpolar fatty acid chains are buried in the middle, away from water.

Membrane splitting and cyrofracture

- membrane splitting occurs along line of fatty acid tails of membrane phospholipids - because only weak hydrophobic interactions bind the halves of the membrane along this line - when cells are frozen and fractured (cyrofracture), the lipid bilayer is often cleaved along the hydrophobic center - electron microscopy of cyrofrature preparation replicas is useful method of studying membranous structures - most of the protruding membrane particles seen are proteins that remain attached to half of membrane adjacent to cytoplasm (= P or protoplasmic face) - fewer particles are found attached to the outer leaf of membrane (= E or extracellular face) - for every protein particle that bulges on one surface, a corresponding depression appears in opposite surface

Other components of unit membranes

The membrane not only contains (phospho)lipids but also proteins. Both proteins and lipids may have externally exposed olgiosaccharide chains, that are sugar chains of so-called glycolipids and of glycoproteins.

Glycocalyx (carbohydrate)

- olgiosaccharide / sugar chains attached to phospholipids (glycolipids) and proteins (glycoporteins) and of cell-secreted glycoproteins and proteoglycans - 20 nm thick - is species-specific as well as cell-specific, thus facilitating cell-cell recognition - important for absorption and uptake on many molecules

Lipids (cholesterol, glycolipids)

- cholesterol molecules are interspersed throughout lipid bilayer often at a ratio of 1:1, affecting packing and fluidity of fatty acid chains (restricting their movements) *lipid rafts - lipid composition of each half of bilayer is different, e.g. in RBCs phosphatidylcholine and sphingomyelins is more abundant in outer half, whereas phosphatidylserine and phosphidylethanolamine is more concentrated in inner half - some of the lipids are glycolipids possessing olgiosacc. chains that extend outward from the surface and thus contribute to lipid asymmetry

Proteins

- fluid mosaic model emphasizes that a membrane consisting of phospholipid bilayer also contains proteins inserted in it or bound to cytoplasmatic surface (peripheral proteins) and that many of these move within the fluid lipid phase - are a major molecular constituent of membranes and can be divided into two groups: 1. Integral proteins (transmembrane and not penetrating proteins) and 2. Peripheral proteins - as with lipids, distribution of membrane proteins is different in the two surfaces of cell membranes, therefore, all membranes in cell are asymmetric - integration: hydrophobic amino acids of integral membrane proteins present on outer region of the proteins interact with the hydrophobic fatty acid portions of the membrane - mosaic disposition of membrane proteins and fluid nature of lipid layer = fluid mosaic model for membrane structure: - some membrane proteins are not bound rigidly in place and are able to move within the plane of the cell membrane, but (unlike lipids!) most of membrane proteins are restricted in their lateral diffusion by attachment to cytoskeletal components - in most epithelial cells, tight junctions (Zonula occludens: occludines and claudines) also restrict lateral diffusion of unattached transmembrane proteins and outer layer lipids to specific membrane domains

Sources

MESCHER, Antony. Junqueira's Basic Histology. 13th edition. 2013. ISBN 978-1-259-07232-1.

Notes: Biophysics. prof. RNDr. Evžen Amler, CSc. 2nd faculty of medicine, Charles University, Prague. Czech Republic.

Cytology I Lecture, Prof. Vajner