Biological membrane

From Infogalactic: the planetary knowledge core
Jump to: navigation, search
Cross-section view of the structures that can be formed by phospholipids in an aqueous solution

A biological membrane or biomembrane is an enclosing or separating membrane that acts as a selectively permeable barrier within living things. Biological membranes, in the form of cell membranes, often consist of a phospholipid bilayer with embedded, integral and peripheral proteins used in communication and transportation of chemicals and ions. Bulk lipid in membrane provides a fluid matrix for proteins to rotate and laterally diffuse for physiological functioning. Proteins are adapted to high membrane fluidity environment of lipid bilayer with the presence of an annular lipid shell, consisting of lipid molecules bound tightly to surface of integral membrane proteins. The cellular membranes should not be confused with isolating tissues formed by layers of cells, such as mucous membranes and basement membranes.



A fluid membrane model of the phospholipid bilayer.

The lipid bilayer consists of two layers- an outer leaflet and an inner leaflet.[1] The components of bilayers are distributed unequally between the two surfaces to create asymmetry between the outer and inner surfaces.[2] This asymmetric organization is important for cell functions such as cell signaling.[3] The asymmetry of the biological membrane reflects the different functions of the two leaflets of the membrane.[4] As seen in the fluid membrane model of the phospholipid bilayer, the outer leaflet and inner leaflet of the membrane are asymmetrical in their composition. Certain proteins and lipids rest only on one surface of the membrane and not the other.


The biological membrane is made up of lipids with hydrophobic tails and hydrophilic heads.[5] The hydrophobic tails are hydrocarbon tails whose length and saturation is important in characterizing the cell.[6] Lipid rafts occur when lipid species and proteins aggregate in domains in the membrane. These help organize membrane components into localized areas that are involved in specific processes, such as signal transduction.

Red blood cells, or erythrocytes, have a unique lipid composition. The bilayer of red blood cells is composed of cholesterol and phospholipids in equal proportions by weight.[6] Erythrocyte membrane plays a crucial role in blood clotting. In the bilayer of red blood cells is phosphatidylserine.[7] This is usually in the cytoplasmic side of the membrane. However, it is flipped to the outer membrane to be used during blood clotting.[7]


Phospholipid bilayers contain different proteins. These membrane proteins have various functions and characteristics and catalyze different chemical reactions. Integral proteins span the membranes with different domains on either side.[5] Integral proteins hold strong association with the lipid bilayer and cannot easily become detached.[8] They will dissociate only with chemical treatment that breaks the membrane. Peripheral proteins are unlike integral proteins in that they hold weak interactions with the surface of the bilayer and can easily become dissociated from the membrane.[5] Peripheral proteins are located on only one face of a membrane and create membrane asymmetry.


Oligosaccharides are sugar containing polymers. In the membrane, they can be covalently bound to lipids to form glycolipids or covalently bound to proteins to form glycoproteins. Membranes contain sugar-containing lipid molecules known as glycolipids. In the bilayer, the sugar groups of glycolipids are exposed at the cell surface, where they can form hydrogen bonds.[8] Glycolipids provide the most extreme example of asymmetry in the lipid bilayer.[9] Glycolipids perform a vast number of functions in the biological membrane that are mainly communicative, including cell recognition and cell-cell adhesion. Glycoproteins are integral proteins.[2] They play an important role in the immune response and protection.[10]


The phospholipid bilayer is formed due to the aggregation of membrane lipids in aqueous solutions.[4] Aggregating is caused by the hydrophobic effect, where hydrophobic ends come into contact with each other and are sequestered away from water and hydrophilic ends are in contact with it.[5] Less water is allowed to interact with the hydrophobic ends and, therefore, hydrogen bonding between hydrophilic heads and water is increased. This creates a favorable molecular arrangement by reducing unfavorable contact between hydrophobic tails and water and increasing hydrogen bonding between the hydrophilic heads and water.[9] The increase in available hydrogen bonding increases the entropy of the system, creating a spontaneous process. Aggregation of non polar substances in water is, therefore, entropically driven and spontaneously occurring.[11] The aggregation formed due to the hydrophobic effect is partially responsible for the shape of biological membranes.[12]


Biological molecules are amphiphilic or amphipathic, i.e. are simultaneously hydrophobic and hydrophilic.[5] The phospholipid bilayer contains charged hydrophilic headgroups, which interact with polar water. The lipids also contain hydrophobic tails, which meet with the hydrophobic tails of the complementary layer. The hydrophobic tails are usually fatty acids that differ in lengths.[9] The interactions of lipids, especially the hydrophobic tails, determine the lipid bilayer physical properties such as fluidity.

Membranes in cells typically define enclosed spaces or compartments in which cells may maintain a chemical or biochemical environment that differs from the outside. For example, the membrane around peroxisomes shields the rest of the cell from peroxides, chemicals that can be toxic to the cell, and the cell membrane separates a cell from its surrounding medium. Peroxisomes are one form of vacuole found in the cell that contain by-products of chemical reactions within the cell. Most organelles are defined by such membranes, and are called "membrane-bound" organelles.

Selective Permeability

Probably the most important feature of a biomembrane is that it is a selectively permeable structure. This means that the size, charge, and other chemical properties of the atoms and molecules attempting to cross it will determine whether they succeed in doing so. Selective permeability is essential for effective separation of a cell or organelle from its surroundings. Biological membranes also have certain mechanical or elastic properties that allow them to change shape and move as required.

Generally, small hydrophobic molecules can readily cross phospholipid bilayers by simple diffusion.[13]

Particles that are required for cellular function but are unable to diffuse freely across a membrane enter through a membrane transport protein or are taken in by means of endocytosis, where the membrane allows for a vacuole to join onto it and push its contents into the cell. Many types of specialized plasma membranes can separate cell from external environment: apical, basolateral, presynaptic and postsynaptic ones, membranes of flagella, cilia, microvillus, filopodia and lamellipodia, the sarcolemma of muscle cells, as well as specialized myelin and dendritic spine membranes of neurons. Plasma membranes can also form different types of "supramembrane" structures such as caveola, postsynaptic density, podosome, invadopodium, desmosome, hemidesmosome, focal adhesion, and cell junctions. These types of membranes differ in lipid and protein composition.

Distinct types of membranes also create intracellular organelles: endosome; smooth and rough endoplasmic reticulum; sarcoplasmic reticulum; Golgi apparatus; lysosome; mitochondrion (inner and outer membranes); nucleus (inner and outer membranes); peroxisome; vacuole; cytoplasmic granules; cell vesicles (phagosome, autophagosome, clathrin-coated vesicles, COPI-coated and COPII-coated vesicles) and secretory vesicles (including synaptosome, acrosomes, melanosomes, and chromaffin granules). Different types of biological membranes have diverse lipid and protein compositions. The content of membranes defines their physical and biological properties. Some components of membranes play a key role in medicine, such as the efflux pumps that pump drugs out of a cell.


The hydrophobic core of the phospholipid bilayer is constantly in motion because of rotations around the bonds of lipid tails.[14] Hydrophobic tails of a bilayer bend and lock together. However, because of hydrogen bonding with water, the hydrophilic head groups exhibit less movement as their rotation and mobility are constrained.[14] This results in increasing viscosity of the lipid bilayer closer to the hydrophilic heads.[5]

Below a transition temperature, a lipid bilayer loses fluidity when the highly mobile lipids exhibits less movement becoming a gel-like solid.[15] The transition temperature depends on such components of the lipid bilayer as the hydrocarbon chain length and the saturation of its fatty acids. Temperature-dependence fluidity constitutes an important physiological attribute for bacteria and cold-blooded organisms. These organisms maintain a constant fluidity by modifying membrane lipid fatty acid composition in accordance with differing temperatures.[5]

See also


  1. Murate, Motohide; Kobayashi, Toshihide. "Revisiting transbilayer distribution of lipids in the plasma membrane". Chemistry and Physics of Lipids. doi:10.1016/j.chemphyslip.2015.08.009.<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  2. 2.0 2.1 Nickels, Jonathan D.; Smith, Jeremy C.; Cheng, Xiaolin. "Lateral organization, bilayer asymmetry, and inter-leaflet coupling of biological membranes". Chemistry and Physics of Lipids. doi:10.1016/j.chemphyslip.2015.07.012.<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  3. Chong, Zhi-Soon; Woo, Wei-Fen; Chng, Shu-Sin (2015-12-01). "Osmoporin OmpC forms a complex with MlaA to maintain outer membrane lipid asymmetry in Escherichia coli". Molecular Microbiology. 98 (6): 1133–1146. doi:10.1111/mmi.13202. ISSN 1365-2958.<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  4. 4.0 4.1 Forrest, Lucy R. (2015-01-01). "Structural Symmetry in Membrane Proteins". Annual Review of Biophysics. 44 (1): 311–337. doi:10.1146/annurev-biophys-051013-023008. PMID 26098517.<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  5. 5.0 5.1 5.2 5.3 5.4 5.5 5.6 Voet, Donald (2012). Fundamentals of Biochemistry: Life at the Molecular Level (4 ed.). Wiley. ISBN 978-1118129180.<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  6. 6.0 6.1 Dougherty, R. M.; Galli, C.; Ferro-Luzzi, A.; Iacono, J. M. (1987-02-01). "Lipid and phospholipid fatty acid composition of plasma, red blood cells, and platelets and how they are affected by dietary lipids: a study of normal subjects from Italy, Finland, and the USA". The American Journal of Clinical Nutrition. 45 (2): 443–455. ISSN 0002-9165. PMID 3812343.<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  7. 7.0 7.1 Lentz, Barry R. (2003-09-01). "Exposure of platelet membrane phosphatidylserine regulates blood coagulation". Progress in Lipid Research. 42 (5): 423–438. ISSN 0163-7827. PMID 12814644.<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  8. 8.0 8.1 Lein, Max; deRonde, Brittany M.; Sgolastra, Federica; Tew, Gregory N.; Holden, Matthew A. (2015-11-01). "Protein transport across membranes: Comparison between lysine and guanidinium-rich carriers". Biochimica et Biophysica Acta (BBA) - Biomembranes. 1848 (11, Part A): 2980–2984. doi:10.1016/j.bbamem.2015.09.004.<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  9. 9.0 9.1 9.2 Alberts, Bruce; Johnson, Alexander; Lewis, Julian; Raff, Martin; Roberts, Keith; Walter, Peter (2002-01-01). "The Lipid Bilayer". Cite journal requires |journal= (help)<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  10. Daubenspeck, James M.; Jordan, David S.; Simmons, Warren; Renfrow, Matthew B.; Dybvig, Kevin (2015-11-23). "General N-and O-Linked Glycosylation of Lipoproteins in Mycoplasmas and Role of Exogenous Oligosaccharide". PLoS ONE. 10 (11): e0143362. doi:10.1371/journal.pone.0143362. PMC 4657876. PMID 26599081.<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  11. Han, Xiang-Gang; Zhang, Xue-Feng (2015-12-07). "Dependence of aggregation behavior on concentration in triblock copolymer solutions: The effect of chain architecture". The Journal of Chemical Physics. 143 (21): 214904. doi:10.1063/1.4936581. ISSN 0021-9606.<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  12. Yonkunas, Michael; Kurnikova, Maria (2015-11-27). "The Hydrophobic Effect Contributes to the Closed State of a Simplified Ion Channel through a Conserved Hydrophobic Patch at the Pore-Helix Crossing". Frontiers in Pharmacology. 6. doi:10.3389/fphar.2015.00284. ISSN 1663-9812. PMC 4661268. PMID 26640439.<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  13. Brown
  14. 14.0 14.1 Vitrac, Heidi; MacLean, David M.; Jayaraman, Vasanthi; Bogdanov, Mikhail; Dowhan, William (2015-11-10). "Dynamic membrane protein topological switching upon changes in phospholipid environment". Proceedings of the National Academy of Sciences. 112 (45): 13874–13879. doi:10.1073/pnas.1512994112. ISSN 0027-8424. PMC 4653158. PMID 26512118.<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>
  15. Rojko, Nejc; Anderluh, Gregor (2015-12-07). "How Lipid Membranes Affect Pore Forming Toxin Activity". Accounts of Chemical Research. doi:10.1021/acs.accounts.5b00403.<templatestyles src="Module:Citation/CS1/styles.css"></templatestyles>

External links