Biological membrane
Abiological membrane,biomembraneorcell membraneis aselectively permeablemembranethat separates the interior of acellfrom theexternalenvironment or createsintracellular compartmentsby serving as a boundary between one part of the cell and another. Biological membranes, in the form ofeukaryoticcell membranes,consist of aphospholipid bilayerwith embedded,integralandperipheral proteinsused in communication and transportation of chemicals andions.The bulk oflipidsin a cell membrane provides a fluid matrix forproteinsto rotate and laterally diffuse for physiological functioning. Proteins are adapted to highmembrane fluidityenvironment of thelipid bilayerwith the presence of anannular lipid shell,consisting of lipid molecules bound tightly to the surface ofintegral membrane proteins.The cell membranes are different from the isolatingtissuesformed by layers of cells, such asmucous membranes,basement membranes,andserous membranes.
Composition
[edit]Asymmetry
[edit]
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 fluidmembrane modelof 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.
• Both the plasma membrane and internal membranes have cytosolic and exoplasmic faces • This orientation is maintained during membrane trafficking – proteins, lipids, glycoconjugates facing the lumen of the ER and Golgi get expressed on the extracellular side of the plasma membrane. In eukaryotic cells, new phospholipids are manufactured by enzymes bound to the part of the endoplasmic reticulum membrane that faces the cytosol.[5]These enzymes, which use free fatty acids assubstrates,deposit all newly made phospholipids into the cytosolic half of the bilayer. To enable the membrane as a whole to grow evenly, half of the new phospholipid molecules then have to be transferred to the opposite monolayer. This transfer is catalyzed by enzymes calledflippases.In the plasma membrane, flippases transfer specific phospholipids selectively, so that different types become concentrated in each monolayer.[5]
Using selective flippases is not the only way to produce asymmetry in lipid bilayers, however. In particular, a different mechanism operates for glycolipids—the lipids that show the most striking and consistent asymmetric distribution inanimal cells.[5]
Lipids
[edit]The biological membrane is made up of lipids with hydrophobic tails and hydrophilic heads.[6]The hydrophobic tails are hydrocarbon tails whose length and saturation is important in characterizing the cell.[7]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.[7]Erythrocyte membrane plays a crucial role in blood clotting. In the bilayer of red blood cells is phosphatidylserine.[8]This is usually in the cytoplasmic side of the membrane. However, it is flipped to the outer membrane to be used during blood clotting.[8]
Proteins
[edit]Phospholipid bilayerscontain different proteins. Thesemembrane proteinshave various functions and characteristics and catalyze different chemical reactions. Integral proteins span the membranes with different domains on either side.[6]Integral proteins hold strong association with the lipid bilayer and cannot easily become detached.[9]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.[6]Peripheral proteins are located on only one face of a membrane and create membrane asymmetry.
| FUNCTIONAL CLASS | PROTEIN EXAMPLE | SPECIFIC FUNCTION |
|---|---|---|
| Transporters | Na+ Pump | actively pumps Na+ out of cells and K+ in |
| Anchors | integrins | link intracellular actin filaments to extracellular matrix proteins |
| Receptors | platelet-derived growth factorreceptor | binds extracellular PDGF and, as a consequence, generates intracellular signals that cause the cell to grow and divide |
| Enzymes | adenylyl cyclase | catalyzes the production of intracellular signaling molecule cyclic AMP in response to extracellular signals |
Oligosaccharides
[edit]Oligosaccharidesare sugar containing polymers. In the membrane, they can be covalently bound to lipids to formglycolipidsor covalently bound to proteins to formglycoproteins.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.[9]Glycolipids provide the most extreme example of asymmetry in the lipid bilayer.[10]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.[11]
Formation
[edit]The phospholipid bilayer is formed due to the aggregation ofmembrane lipidsin aqueous solutions.[4]Aggregation is caused by thehydrophobic effect,where hydrophobic ends come into contact with each other and are sequestered away from water.[6]This arrangement maximises hydrogen bonding between hydrophilic heads and water while minimising unfavorable contact between hydrophobic tails and water.[10]The increase in available hydrogen bonding increases the entropy of the system, creating a spontaneous process.
Function
[edit]Biological molecules are amphiphilic or amphipathic, i.e. are simultaneously hydrophobic and hydrophilic.[6]The phospholipid bilayer contains chargedhydrophilicheadgroups, which interact with polarwater.The layers also containhydrophobictails, which meet with the hydrophobic tails of the complementary layer. The hydrophobic tails are usually fatty acids that differ in lengths.[10]Theinteractionsof lipids, especially the hydrophobic tails, determine thelipid bilayer physical propertiessuch 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 aroundperoxisomesshields 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 calledmembrane-bound organelles.
Selective permeability
[edit]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 simplediffusion.[12]
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 ofendocytosis,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,filopodiaandlamellipodia,thesarcolemmaof muscle cells, as well as specialized myelin anddendritic spinemembranes of neurons. Plasma membranes can also form different types of "supramembrane" structures such ascaveolae,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 andCOPII-coated vesicles) and secretory vesicles (includingsynaptosome,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.
Fluidity
[edit]The hydrophobic core of the phospholipid bilayer is constantly in motion because of rotations around the bonds of lipid tails.[13]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.[13]This results in increasing viscosity of the lipid bilayer closer to the hydrophilic heads.[6]
Below a transition temperature, a lipid bilayer loses fluidity when the highly mobile lipids exhibits less movement becoming a gel-like solid.[14]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.[6]
In animal cells, membrane fluidity is modulated by the inclusion of the sterolcholesterol.This molecule is present in especially large amounts in the plasma membrane, where it constitutes approximately 20% of the lipids in the membrane by weight. Because cholesterol molecules are short and rigid, they fill the spaces between neighboring phospholipid molecules left by the kinks in their unsaturated hydrocarbon tails. In this way, cholesterol tends to stiffen the bilayer, making it more rigid and less permeable.[5]
For all cells, membrane fluidity is important for many reasons. It enables membrane proteins to diffuse rapidly in the plane of the bilayer and to interact with one another, as is crucial, for example, incell signaling.It permits membrane lipids and proteins to diffuse from sites where they are inserted into the bilayer after their synthesis to other regions of the cell. It allows membranes to fuse with one another and mix their molecules, and it ensures that membrane molecules are distributed evenly between daughter cells when a cell divides. If biological membranes were not fluid, it is hard to imagine how cells could live, grow, and reproduce.[5]
The fluidity property is at the center of the Helfrichmodelwhich allows for calculating the energy cost of an elastic deformation to the membrane.
See also
[edit]References
[edit]- ^Murate, Motohide; Kobayashi, Toshihide (2016). "Revisiting transbilayer distribution of lipids in the plasma membrane".Chemistry and Physics of Lipids.194:58–71.doi:10.1016/j.chemphyslip.2015.08.009.PMID26319805.
- ^abNickels, Jonathan D.; Smith, Jeremy C.; Cheng, Xiaolin (2015)."Lateral organization, bilayer asymmetry, and inter-leaflet coupling of biological membranes".Chemistry and Physics of Lipids.192:87–99.doi:10.1016/j.chemphyslip.2015.07.012.PMID26232661.
- ^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.PMID26314242.
- ^abForrest, 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.PMC5500171.PMID26098517.
- ^abcdeAlberts, Bray, Hopkin, Johnson, Lewis, Raff, Roberts, Walter, Bruce, Dennis, Karen, Alexander, Julian, Martin, Keith, Peter (2010).Essential Cell Biology third edition.New York: Garland Science, Taylor & Francis Group, LLC, an informa business. p. 370.ISBN978-0815341291.
{{cite book}}:CS1 maint: multiple names: authors list (link) - ^abcdefgVoet, Donald (2012).Fundamentals of Biochemistry: Life at the Molecular Level (4 ed.).Wiley.ISBN978-1118129180.
- ^abDougherty, R. M.; Galli, C.; Ferro-Luzzi, A.; Iacono, J. M. (1987). "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.doi:10.1093/ajcn/45.2.443.PMID3812343.S2CID4436467.
- ^abLentz, Barry R. (2003). "Exposure of platelet membrane phosphatidylserine regulates blood coagulation".Progress in Lipid Research.42(5): 423–438.doi:10.1016/s0163-7827(03)00025-0.PMID12814644.
- ^abLein, 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.PMC4704449.PMID26342679.
- ^abcAlberts, Bruce; Johnson, Alexander; Lewis, Julian; Raff, Martin; Roberts, Keith; Walter, Peter (2002-01-01)."The Lipid Bilayer".Garland Science.
{{cite journal}}:Cite journal requires|journal=(help) - ^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.Bibcode:2015PLoSO..1043362D.doi:10.1371/journal.pone.0143362.PMC4657876.PMID26599081.
- ^Brown, Bernard (1996).Biological Membranes(PDF).London, U.K.: The Biochemical Society. p. 21.ISBN978-0904498325.Archived fromthe original(PDF)on 2015-11-06.Retrieved2014-05-01.
- ^abVitrac, 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.Bibcode:2015PNAS..11213874V.doi:10.1073/pnas.1512994112.PMC4653158.PMID26512118.
- ^Rojko, Nejc; Anderluh, Gregor (2015-12-07). "How Lipid Membranes Affect Pore Forming Toxin Activity".Accounts of Chemical Research.48(12): 3073–3079.doi:10.1021/acs.accounts.5b00403.PMID26641659.
External links
[edit]
Media related toBiological membranesat Wikimedia Commons- Membranesat the U.S. National Library of MedicineMedical Subject Headings(MeSH)
