University:
Kentucky State University
Course:
CHE 315 | Biochemistry
Academic year:

2020
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317

Pages:

68
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MoGhoadoAnotozj9

Lipids This lecture Lipids Lipids are a heterogeneous class of naturally occurring organic compounds that share some properties based on structural similarities, mainly a dominance of nonpolar groups. They are Amphipathic in nature. They are insoluble in water, but soluble in fat or organic solvents (ether, chloroform, benzene, acetone). They are widely distributed in plants & animals. Classes Simple lipids (fats, oils, and waxes) Complex lipids (glycerides , glycerophospholipids, sphingolipids, glycolipids, lipoproteins) Derived lipids (fatty acids, alcohols, eicosanoids) Cyclic lipids (steroids) Lipid Functions Lipids include: Storage lipids Structural lipids in membranes Lipids as signals, cofactors & pigments They are a major source of energy They are storable to unlimited amount (vs. carbohydrates) They provide considerable amount of energy to the body (25% of body needs) & provide a high-energy value (more energy per gram vs. carbohydrates & proteins) Structural components (cell membranes) Precursors of hormone and vitamins Shock absorbers thermal insulator Fatty acids Aliphatic mono-carboxylic acids Formula: R-(CH2)n-COOH Lengths Physiological (12-24) Abundant (16 and 18) Degree of unsaturation Amphipathic molecules Polar Functions: • Building blocks of other lipids • Modification of many proteins (lipoproteins) • Important fuel molecules • Derivatives of important cellular molecules Non-polar Types of fatty acids  Saturated fatty acids are those with all of C-C bonds being single.  Unsaturated fatty acids are those with one or more double bonds between carbons  Monounsaturated fatty acid: a fatty acid containing one double bond.  Polyunsaturated fatty acids contain two or more double bonds. Cis vs. trans bonds cis isomer predominates; trans is rare Properties of fatty acids The properties of fatty acids (melting point and solubility) are dependent on chain length and degree of saturation Properties of fatty acids Short chain F.A. Medium-chain F.A. Long chain F.A. They are liquid in nature Solids at room temperature Solids at room temperature Water-soluble Water-soluble Water-insoluble Volatile at RT Non-volatile at RT Non-volatile Acetic, butyric, caproic FA Caprylic & capric F.A. Palmitic and stearic F.A Greek number prefix Number 1 2 3 4 prefix MonoDiTriTetra- Number 5 6 7 8 prefix PentaHexaHeptaOcta- Number 9 10 20 prefix NonaDecaEico- Naming of a fatty acid Alkane to oic Octadecane (octa and deca) is octadecanoic acid One double bond = octadecenoic acid Two double bonds = octadecadienoic acid Three double bonds = octadecatrienoic acid Designation of carbons and bonds 18:0 = a C18 fatty acid with no double bonds stearic acid (18:0); palmitic acid (16:0) 18:2 = two double bonds (linoleic acid) Designation of location of bonds Δn: The position of a double bond cis-Δ9 :a cis double bond between C 9 and 10 trans-Δ2:a trans double bond between C 2 and 3 Number of Number Common carbons of double name bonds 14 0 Myristate Systematic name Formula n-Tetradecanoate CH3(CH2)12COO- 16 0 Palmitate n-Hexadecanoate CH3 (CH2) 14COO- 18 0 Stearate n-Octadecanoate CH3(CH2) 16COO- 18 1 Oleate cis-Δ9-Octadecenoate CH3(CH2) 7CH=CH(CH2) 7COO- 18 2 Linoleate 18 3 20 4 cis,cis-Δ9,Δ12Octadecadienoate all-cis-Δ9,Δ12,Δ15Linolenate Octadecatrienoate Arachidonate all-cis-Δ5,Δ8,Δ11,Δ14Eicosatetraenoate CH3(CH2) 2(CH=CHCH2) 2(CH2) 6COOCH3CH2(CH=CHCH2) 3(CH2) 6COOCH3 (CH2) 4(CH=CHCH2) 4(CH2) 2COO- Another way of naming (ω)-C: distal methyl C as #1 • Linoleic acid: precursor of arachidonates • Linolenic acid: precursor of EPA and DHA Numerical Symbol Common Name and Structure 18:1Δ9 18:2Δ9,12 18:3Δ9,12,15 20:4Δ5,8,11,14 20:5Δ5,8,11,14,17 22:6Δ4,7,10,13,16,19 Oleic acid Linoleic acid α-Linolenic acid (ALA) Arachidonic acid Comments Omega-9 monounsaturated Omega-6 polyunsaturated Omega-3 polyunsaturated Omega-6 polyunsaturated Eicosapentaenoic acid (EPA) Omega-3 polyunsaturated (fish oils) Docosahexaenoic acid (DHA) Omega-3 polyunsaturated (fish oils) Arachidonate all cis-Δ5,Δ8,Δ11,Δ14-eicosatetraenoate, CH3(CH2)4(CH=CHCH2)4(CH2)2COO- Eicosanoids and their functions Prostaglandins Inhibition of platelet aggregation Blood clotting Leukotrienes Constriction of smooth muscles Asthma Thromboxanes Constriction of smooth muscles Platelet aggregation Prostacyclins An inhibitor of platelet aggregation A vasodilator Aspirin is good COX: Cyclooxygenase Targets of Aspirin Cyclooxygenase is present in three forms in cells, COX-1, COX-2, and COX-3. Aspirin targets both, but COX-2 should only be the target. Celebrex A new generation drug, Celebrex, targets COX2, but is prescribed with a strong warning of side effects on the label. Omega fatty acids Omega-3 fatty acids α-linolenic acid → eicosapentaenoic acid (EPA) → docosahexaenoic acid (DHA) They reduce inflammatory reactions by: Reducing conversion of arachidonic acid into eicosanoids Promoting synthesis of anti-inflammatory molecules Omega-6 fatty acids: Arachidonic acid stimulates platelet and leukocyte activation, signals pain, Induces bronchoconstriction, regulates gastric secretion Omega-9 fatty acids Oleic acid Reduces cholesterol in the circulation Triglycerides Ester linkage Types of glycerides How soluble will a triglyceride be if fatty acids are unsaturated? Solid vs. liquid fats Vegetable oils consist almost entirely of unsaturated fatty acids, whereas animal fats contain a much larger percentage of saturated fatty acids. This is the primary reason for the different melting points of fats and oils Saponification Hydrolysis : steam, acid, enzyme (e.g., lipase of pancreas) Saponification: Alkaline hydrolysis produces salts of fatty acids (soaps). Soaps cause emulsification of oily material How does soap work? When mixed with water, the hydrophobic hydrocarbon tails cluster together to create a nonpolar microenvironment and the hydrophilic ionic heads interact with water. The resulting spherical clusters are called micelles. Grease and dirt are trapped inside micelles and the complex can be rinsed away. Hydrogenation The carbon-carbon double bonds in vegetable oils can be hydrogenated to yield saturated fats in the same way that any alkene can react with hydrogen to yield an alkane. Trans fat Although the animal fat is unhealthy, it has better cooking properties and better taste. Therefore, chemists invented a method of converting unsaturated fat into solid form by partially hydrogenating it. Partial hydrogenation converts some, but not all, double bonds into single bonds generating (trans fats). The primary health risk identified for trans fat consumption is an elevated risk of coronary heart disease (CHD). Example: margarine In margarine, only about two-thirds of the double bonds present in the starting vegetable oil are hydrogenated, so that the margarine remains soft in the refrigerator and melt on warm toast. Waxes Solid simple lipids containing a monohydric alcohol (C16 ~ C30, higher molecular weight than glycerol) esterified to long-chain fatty acids (C14 ~ C36). Examples: palmitoyl alcohol Insoluble in water & Negative to acrolin test Are not easily hydrolyzed (fats) & are indigestible by lipases Are very resistant to rancidity Are of no nutritional value Coatings that prevent loss of water by leaves of plants Membrane lipids The most prevalent class of lipids in membranes is the glycerophospholipids Phospholipids (phosphoacylglycerols) Classification of Glycerophospholipids Phosphatidic acids Phosphatidylcholine (lecithins) Most abundant membrane lipid Cephalins Phosphatidylethanolamine Phosphatidylserine abundant in brain Phosphatidylinositol sends messages across cell membranes Cardiolipin Plasmalogens Glycerophospholipids - Lecithins Snake venom contain lecithinase, which hydrolyzes polyunsaturated fatty acids and converting lecithin into lysolecithin hemolysis of RBCs Emulsification Because of their amphipathic nature, they act as emulsifying agents, that is substances that can surround nonpolar molecules and keep them in suspension in water. Glycerophospholipids - Cardiolipins Diphosphatidyl-glycerol Found in the inner membrane of mitochondria Initially isolated from heart muscle (cardio) Structure: 3 molecules of glycerol, 4 fatty acids & 2 phosphate groups Plasmalogens They are found in the cell membrane phospholipids fraction of brain & muscle, liver, and semen. They have a protective role against reactive oxygen species Structure: Precursor: Dihydroxyacetone phosphate Unsaturated fatty alcohol at C1 connected by ether bond In mammals: at C3; phosphate + ethanolamine or choline Major classes of plasmalogens Ethanolamine plasmalogen (myelin-nervous tissues) Choline plasmalogen (cardiac tissue) Platelet activating factor Serine plasmalogens Glycerophospholipids - Inositides Phosphatidyl inositol Nitrogenous base: cyclic sugar alcohol (inositol) Structure: glycerol, saturated FA, unsaturated FA, phosphoric acid, & inositol Source: Brain tissues  Functions: ▪ Major component of cell membrane ▪ Second messenger during signal transduction ▪ On hydrolysis by phospholipase C, phosphatidyl-inositol-4,5diphosphate produces diacyl-glycerol (DAG) & inositoltriphosphate (IP3); which liberates calcium The different structures of phospholipids Uses of liposomes: delivery Sphingolipids Sphingolipids are found in the plasma membranes of all eukaryotic cells and is highest in the cells of the central nervous system The core of sphingolipids is the long-chain amino alcohol, sphingosine Amide bond Mysterious lipids Ceramide Types of sphingolipids The sphingolipids are divided into the two subcategories: Sphingomyelins Glycosphingolipid (or glycolipids) Sphoingomyelin Sphoingomyelin is a sphinglolipid that is a major component of the coating around nerve fibers The group attached to C1 is a phosphocholine Zooming into the myelin Glycolipids Sphingolipids can also contain carbohydrates attached at C-1 and these are known as glycolipids Glycolipids are present on cell membranes and act as cell surface receptors that can function in cell recognition (e.g., pathogens) and chemical messengers There are three types of glycolipids Cerebrosides Globosides Gangliosides Glycolipids • Cerebrosides: the simplest glycolipids, contain a single hexose (galactose or glucose). • Globosides and gangliosides are more complex glycolipids. • Both contain glucose, galactose, and N-acetylgalactosamine, but gangliosides must also contain sialic acid. Gangliosides are targeted by cholera toxin in the human intestine. Sulfatides Synthesized from galactocerebroside Abundant in brain myelin Sphingolipids and blood groups Lipoproteins Function: transport of different types of lipids (cholesterol, cholesterol esters, phospholipids & triacylglycerols) in blood plasma. As lipid content increases, the density decreases Steroids The precursor The most common steroid The nucleus Products of cholesterol Hormones sex hormones (androgens,. estrogens, progestins) Some vitamins such as vitamin D Vitamins A, D, E, and K are made from isoprenoids Bile acids (intestinal absorption of fat) Cholesterol esters A cholesterol with a fatty acid attached at (-OH) of C3 Name the molecules? Atherosclerosis Cell membranes The membrane is hypothesized in a model known as the fluid mosaic model. Components: 45% lipid, 45% protein and 10% carbohydrate They exist side by side without forming some other substance of intermediate nature. Phospholipids The outer: phosphatidylcholine, sphingomyelin, and glycolipids(cell recognition) The inner: phosphatidylethanolamine, phosphatidylserine, and phosphatidylinositol (signaling) Cholesterol is distributed in both leaflets Animal cells vs. plant cells vs. prokaryotic cells Fatty acids and membrane fluidity Membrane fluidity and temperature Melting temperature (transition temperature Cholesterol and membrane fluidity The presence of cholesterol stabilizes the extended straight-chain arrangement of saturated fatty acids by van der Waals interactions. Cholesterol makes a membrane less solid at low temperatures and more solid at high temperatures. • It decreases the mobility of hydrocarbon tails of phospholipids. • It interferes with close packing of fatty acid tails in the crystal state. Membrane proteins Types of membrane proteins Peripheral proteins: are associated with the exterior of membranes via noncovalent interactions Integral membrane proteins: anchored into membrane via hydrophobic regions Lipid-anchored: associated via a lipid group Peripheral membrane proteins They are associated with membranes but do not penetrate the hydrophobic core of the membrane often associated with integral membrane proteins They are not strongly bound to the membrane and can be removed without disrupting the membrane structure treatment with mild detergent Integral membrane proteins The integral proteins can be associated with the lipid bilayer in several ways. The membrane integral domains are: 1. Single or multiple 2. -helix or -sheet Some can form channels. Structure-Function of Membranes Transport: Membranes are impermeable barrier Proteins can be carriers or channels Signaling Protein receptors and small molecules (some can be lipids themselves) Catalysis Enzyme-linked receptors

Lipids

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