Prentice Hall c2002Chapter 91 Chapter 9 - Lipids and Membranes Lipids are essential components of all living organisms Lipids are water insoluble organic compounds They are hydrophobic (nonpolar) or amphipathic (containing both nonpolar and polar regions )

Prentice Hall c2002Chapter 92 Fig 9.1 Structural relationships of major lipid classes

Prentice Hall c2002Chapter 93 Fatty Acids Fatty acids differ from one another in: (1) Length of the hydrocarbon tails (2) Degree of unsaturation (double bond) (3) Position of the double bonds in the chain Fatty acids - R-COOH (R=hydrocarbon chain) are components of triacylglycerols, glycerophospholipids, sphingolipids Nomenclature of fatty acids Most fatty acids have 12 to 20 carbons Most chains have an even number of carbons IUPAC nomenclature: carboxyl carbon is C-1 Common nomenclature:  etc. from C-1 Carbon farthest from carboxyl is  Fig 9.2

Prentice Hall c2002Chapter 94 Table 9.1

Prentice Hall c2002Chapter 95 Structure and nomenclature of fatty acids Saturated - no C-C double bonds Unsaturated - at least one C-C double bond Monounsaturated - only one C-C double bond Polyunsaturated - two or more C-C double bonds Double bonds in fatty acids Double bonds are generally cis Position of double bonds indicated by  n, where n indicates lower numbered carbon of each pair Shorthand notation example: 20:4  5,8,11,14 (total # carbons : # double bonds,  double bond positions )

Prentice Hall c2002Chapter 96 (a) Stearate (octadecanoate) (b) Oleate (cis-  9 -octadecenoate) (c) Linolenate (all-cis-  9,12,15 - octadecatrienoate) The cis double bonds produce kinks in the tails of unsaturated fatty acids Fig. 9.3 Structures of three C 18 fatty acids

Prentice Hall c2002Chapter 97 Fig 9.4 Structures of stearate, oleate, linolenate

Prentice Hall c2002Chapter 98 Triacylglycerols Fatty acids are stored as neutral lipids, triaclyglycerols (TGs) Fats have 2-3 times the energy of proteins or carbohydrates TGs are 3 fatty acyl residues esterified to glycerol TGs are hydrophobic, stored in fat cells (adipocytes) Fig 9.5 Structure of a triacylglycerol

Prentice Hall c2002Chapter 99 Fig. 9.8a Structure of glycerophospholipids Phosphatidylethanolamine (PE)

Prentice Hall c2002Chapter 910 Fig. 9.8b Structures of glycerophospholipids Phosphatidylserine (PS)

Prentice Hall c2002Chapter 911 Fig. 9.8c Structures of glycerophospholipids Phosphatidylcholine (PC)

Prentice Hall c2002Chapter 912 Fig 9.9 Phospholipases hydrolyze phospholipids

Prentice Hall c2002Chapter 913 Fig 9.10 Structure of an ethanolamine plasmalogen Plasmalogens - C-1 hydrocarbon substituent attached by a vinyl ether linkage (not ester linkage)

Prentice Hall c2002Chapter 914 Sphingolipids Sphingolipids - sphingosine is the backbone abundant in central nervous system tissues Ceramides - fatty acyl group linked to C-2 of sphingosine by an amide bond Sphingomyelins - phosphocholine attached to C-1 of ceramide Cerebrosides - glycosphingolipids with one monosaccharide residue attached via a glycosidic linkage to C-1 of ceramide Galactosylcerebrosides - a single  -D-galactose as a polar head group Gangliosides - contain oligosaccharide chains with N-acetyl-neuraminic acid (NeuNAc) attached to a ceramide

Prentice Hall c2002Chapter 915 Fig 9.11 ( a) Sphingosine (b) Ceramides (c) Sphingomyelin

Prentice Hall c2002Chapter 916 Fig 9.12 Structure of a galactocerebroside

Prentice Hall c2002Chapter 917 Fig 9.13 Ganglioside G M2 (NeuNAc in blue)

Prentice Hall c2002Chapter 918 Steroids Classified as isoprenoids - related to 5-carbon isoprene (found in membranes of eukaryotes) Steroids contain four fused ring systems: 3-six carbon rings (A,B,C) and a 5-carbon D ring Ring system is nearly planar Substituents point either down (  ) or up (  ) Fig 9.14 Isoprene Fig 9.15

Prentice Hall c2002Chapter 919 Fig 9.15 Structures of several steroids

Prentice Hall c2002Chapter 920 Fig 9.15 Structures of several steroids

Prentice Hall c2002Chapter 921 Cholesterol Cholesterol modulates the fluidity of mammalian cell membranes It is also a precursor of the steroid hormones and bile salts It is a sterol (has hydroxyl group at C-3) The fused ring system makes cholesterol less flexible than most other lipids

Prentice Hall c2002Chapter 922 Cholesterol esters Cholesterol is converted to cholesteryl esters for cell storage or transport in blood Fatty acid is esterified to C-3 OH of cholesterol Cholesterol esters are very water insoluble and must be complexed with phospholipids or amphipathic proteins for transport Fig 9.17 Cholesteryl ester

Prentice Hall c2002Chapter 923 Waxes Waxes are nonpolar esters of long-chain fatty acids and long chain monohydroxylic alcohols Waxes are very water insoluble and high melting They are widely distributed in nature as protective waterproof coatings on leaves, fruits, animal skin, fur, feathers and exoskeletons Fig 9.18 Myricyl palmitate, a wax

Prentice Hall c2002Chapter 924 Eicosanoids Eicosanoids are oxygenated derivatives of C 20 polyunsaturated fatty acids (e.g. arachidonic acid) Prostaglandin E2 - can cause constriction of blood vessels Thromboxane A2 - involved in blood clot formation Leukotriene D4 - mediator of smooth-muscle contraction and bronchial constriction seen in asthmatics Aspirin alleviates pain, fever, and inflammation by inhibiting cyclooxygenase (COX), an enzyme critical for the synthesis of prostaglandins. (NSAID family of compounds)

Prentice Hall c2002Chapter 925 Fig 9.19 Arachidonic acid and eicosanoid derivatives

Prentice Hall c2002Chapter 926 Lipid vitamins Vitamins A,D,E, and K are isoprenoid derivatives Vitamin E

Prentice Hall c2002Chapter 927 Biological Membranes Are Composed of Lipid Bilayers and Proteins Biological membranes define the external boundaries of cells and separate cellular compartments A biological membrane consists of proteins embedded in or associated with a lipid bilayer

Prentice Hall c2002Chapter 928 Several important functions of membranes Some membranes contain protein pumps for ions or small molecules Some membranes generate proton gradients for ATP production Membrane receptors respond to extracellular signals and communicate them to the cell interior Lipid Bilayers Lipid bilayers are the structural basis for all biological membranes Noncovalent interactions among lipid molecules make them flexible and self-sealing Polar head groups contact aqueous medium Nonpolar tails point toward the interior

Prentice Hall c2002Chapter 929 Fig 9.21 Membrane lipid and bilayer

Prentice Hall c2002Chapter 930 Fluid Mosaic Model of Biological Membranes Fluid mosaic model - membrane proteins and lipids can rapidly diffuse laterally or rotate within the bilayer (proteins “float” in a lipid-bilayer sea) Membranes: ~25-50% lipid and 50-75% proteins Lipids include phospholipids, glycosphingolipids, cholesterol (in some eukaryotes) Compositions of biological membranes vary considerably among species and cell types

Prentice Hall c2002Chapter 931 Fig 9.22 Structure of a typical eukaryotic plasma membrane

Prentice Hall c2002Chapter 932 Lipid Bilayers and Membranes Are Dynamic Structures Fig 9.23 (a) Lateral diffusion is very rapid (b) Transverse diffusion (flip-flop) is very slow

Prentice Hall c2002Chapter 933 Fig 9.25 Freeze-fracture electron microscopy, distribution of membrane proteins

Prentice Hall c2002Chapter 934 Fig 9.22 Structure of a typical eukaryotic plasma membrane

Prentice Hall c2002Chapter 935 Three Classes of Membrane Proteins (1) Integral membrane proteins Contain hydrophobic regions embedded in the lipid bilayer Usually span the bilayer completely (2) Peripheral membrane proteins Associated with membrane through charge-charge or hydrogen bonding interactions to integral proteins or membrane lipids More readily dissociated from membranes than covalently bound proteins Change in pH or ionic strength often releases these proteins (3) Lipid-anchored membrane proteins Tethered to membrane through a covalent bond to a lipid

Prentice Hall c2002Chapter 936 Fig 9.22 Structure of a typical eukaryotic plasma membrane

Prentice Hall c2002Chapter 937 Membrane Transport Three types of integral membrane protein transport: (1) Channels and pores (2) Passive transporters (3) Active transporters

Prentice Hall c2002Chapter 938 Table 9.3 Characteristics of membrane transport

Prentice Hall c2002Chapter 939 Pores and Channels Pores and channels are transmembrane proteins with a central passage for ions and small molecules Solutes of appropriate size, charge, and molecular structure can diffuse down a concentration gradient Process requires no energy Central passage allows molecules and ions of certain size, charge and geometry to transverse the membrane. Figure 9.30

Prentice Hall c2002Chapter 940 Passive Transport Passive transport (facilitated diffusion) does not require an energy source Protein binds solutes and transports them down a concentration gradient Types of passive transport systems Uniport - transporter carries only a single type of solute Some transporters carry out cotransport of two solutes, either in the same direction (symport) or in opposite directions (antiport)

Prentice Hall c2002Chapter 941 Fig 9.31 Types of passive transport (a) Uniport (b) Symport (c) Antiport

Prentice Hall c2002Chapter 942 Fig 9.32 Kinetics of passive transport Initial rate of transport increases until a maximum is reached (site is saturated)

Prentice Hall c2002Chapter 943 Active Transport Transport requires energy to move a solute up its concentration gradient Transport of charged molecules or ions may result in a charge gradient across the membrane Types of active transport Primary active transport is powered by a direct source of energy as ATP, light or electron transport Secondary active transport is driven by an ion concentration gradient

Prentice Hall c2002Chapter 944 Fig 9.34 Secondary active transport in E. coli Oxidation of S red generates a transmembrane proton gradient Movement of H + down its gradient drives lactose transport (lactose permease)

Prentice Hall c2002Chapter 945 Fig 9.35 Secondary active transport in animals: Na + -K + ATPase Na + gradient (Na + -K + ATPase) drives glucose transport

Prentice Hall c2002Chapter 946 Endocytosis and Exocytosis Cells import/export molecules too large to be transported via pores, channels or proteins by: Endocytosis - macromolecules are engulfed by plasma membrane and brought into the cell inside a lipid vesicle Exocytosis - materials to be excreted from the cell are enclosed in vesicles that fuse with the plasma membrane

Prentice Hall c2002Chapter 947 Transduction of Extracellular Signals Specific receptors in plasma membranes respond to external chemicals (ligands) that cannot cross the membrane: hormones, neurotransmitters, growth factors Signal is passed through membrane protein transducer to a membrane-bound effector enzyme Effector enzyme generates a second messenger which diffuses to intracellular target

Prentice Hall c2002Chapter 948 Fig 9.37 General mechanism of signal transduction across a membrane

Prentice Hall c2002Chapter 949 Fig 9.43 Summary of the adenyl cyclase signaling pathway OUT IN