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Lipidated proteins

Cholesterol is biosynthesized in the liver trans ported throughout the body to be used in a va riety of ways and returned to the liver where it serves as the biosynthetic precursor to other steroids But cholesterol is a lipid and isn t soluble in water How can it move through the blood if it doesn t dis solve in if The answer is that it doesn t dissolve but IS instead carried through the blood and tissues as part of a lipoprotein (lipid + protein = lipoprotein) The proteins that carry cholesterol from the liver are called low density lipoproteins or LDLs those that return it to the liver are the high-density lipoproteins or HDLs If too much cholesterol is being transported by LDL or too little by HDL the extra cholesterol builds up on the walls of the arteries caus mg atherosclerosis A thorough physical examination nowadays measures not only total cholesterol con centration but also the distribution between LDL and HDL cholesterol An elevated level of LDL cholesterol IS a risk factor for heart disease LDL cholesterol is bad cholesterol HDLs on the other hand remove excess cholesterol and are protective HDL cholesterol IS good cholesterol... [Pg.1096]

Further investigations were carried out at lipid double layers and at phospholipids of membranes. Lipid-lipid and lipid-protein interactions were recognized by diazirine labeling (79PNA2595). [Pg.236]

Baumgartner and coworkers [145,146] study lipid-protein interactions in lipid bilayers. The lipids are modeled as chains of hard spheres with heads tethered to two virtual surfaces, representing the two sides of the bilayer. Within this model, Baumgartner [145] has investigated the influence of membrane curvature on the conformations of a long embedded chain (a protein ). He predicts that the protein spontaneously localizes on the inner side of the membrane, due to the larger fluctuations of lipid density there. Sintes and Baumgartner [146] have calculated the lipid-mediated interactions between cylindrical inclusions ( proteins ). Apart from the... [Pg.648]

Cholesterol is biosynthesized in the liver, transported throughout the body to be used in a variety of ways, and returned to the liver where it serves as the biosynthetic precursor to other steroids. But cholesterol is a lipid and isn t soluble in water. How can it move through the blood if it doesn t dissolve in it The answer is that it doesn t dissolve, but is instead carried through the blood and tissues as part of a lipoprotein (lipid + protein = lipoprotein). [Pg.1096]

Cell membrane Roughly 50 50 lipid protein as a 5-um-thick The plasma membrane is a selectively... [Pg.27]

There are other ways in which the lateral organization (and asymmetry) of lipids in biological membranes can be altered. Eor example, cholesterol can intercalate between the phospholipid fatty acid chains, its polar hydroxyl group associated with the polar head groups. In this manner, patches of cholesterol and phospholipids can form in an otherwise homogeneous sea of pure phospholipid. This lateral asymmetry can in turn affect the function of membrane proteins and enzymes. The lateral distribution of lipids in a membrane can also be affected by proteins in the membrane. Certain integral membrane proteins prefer associations with specific lipids. Proteins may select unsaturated lipid chains over saturated chains or may prefer a specific head group over others. [Pg.266]

We ll see later in this chapter and again in Chapter 29 that carbonyl condensation reactions occur frequently in metabolic pathways. In fact, almost all classes of biomolecules—carbohydrates, lipids, proteins, nucleic acids, and many others—are biosynthesized through pathways that involve carbonyl condensation reactions. As with the or-substitution reaction discussed in the previous chapter, the great value of carbonyl condensations is that they are one of the few general methods for forming carbon-carbon bonds, thereby making it possible to build larger molecules from smaller precursors. We ll see how and why these reactions occur in this chapter. [Pg.877]

Name Density (g/mL) % Lipid % Protein Optimal (mg/dL) Poor (mg/dL)... [Pg.1091]

D, = The 5-value of the i-th component in the diet. This diet must he summed over all components, so that all the possible sources are included. For example, it might be protein, carbohydrate and lipid protein and non-protein or broken down into much greater detail. [Pg.216]

Langmuir-Blodgett (LB) films of proteins (Tiede 1985, Hwang et al. 1977, Furuno et al. 1988, Lvov et al. 1991) and lipid-protein complexes (Fromherz 1971, Phillips et al. 1975, Mecke et al. 1987, Kozarac et al. 1988) were intensively studied and characterized by different techniques. [Pg.153]

MEMBRANES ARE COMPLEX STRUCTURES COMPOSED OF LIPIDS, PROTEINS, CARBOHYDRATES... [Pg.416]

Besides water, the diet must provide metabolic fuels (mainly carbohydrates and lipids), protein (for growth and turnover of tissue proteins), fiber (for roughage), minerals (elements with specific metabolic functions), and vitamins and essential fatty acids (organic compounds needed in small amounts for essential metabolic and physiologic functions). The polysaccharides, tri-acylglycerols, and proteins that make up the bulk of the diet must be hydrolyzed to their constituent monosaccharides, fatty acids, and amino acids, respectively, before absorption and utilization. Minerals and vitamins must be released from the complex matrix of food before they can be absorbed and utifized. [Pg.474]

Lipids Proteins Undergo Turnover at Different Rates in Different Membranes... [Pg.511]

Because of their very complex chemical structures and heterogeneity, melanins are difficult to extract, separate, and characterize from tissues. Eumelanins are insoluble in water and organic solvents. They can be extracted from tissues with strong chemicals that are capable of removing lipids, proteins, and other tissue components but also lead to the formation of degradation products. Enzymatic procedures were developed for the isolation of eumelanins from mammalian hair and irises. The first step is sequential digestion with protease, proteinase K, and papaine in the presence... [Pg.114]

Recent findings from the ATBC stndy even showed that P-carotene snpple-mentation increased the post-trial risk of a hrst-ever non-fatal MI. Two secondary prevention trials, the Heart Protection Stndy and the ATBC presented similar resnlts. The former showed no association between P-carotene and fatal or non-fatal vascular events and the latter reported signihcantly increased risks of fatal coronary events in the P-carotene-snpplemented gronp. Resnlts of clinical trials focused on the effects of carotenoids on CVD biomarkers are controversial. Although carotenoid supplementation increased sernm levels,only lycopene was shown to be inversely associated with lipid, protein, DNA and LDL oxidation, and plasma cholesterol levels. - - ... [Pg.134]

Martonosi, A. (1975) In Biomembranes - Lipids, Proteins and Receptors, Proc. of a NATO Advanced Study Institute (Burton. R.M. and Packer, L., Eds.), pp. 369-.390, Bi-Science Publications Div., Webster Groves, Missouri. [Pg.113]

The complex cascades that comprise the inflammatory reaction are designed primarily to limit tissue damage and prevent or inhibit infection. ROMs play a critical role in both these beneficial processes. However, high level fluxes of toxic free radicals are capable of causing damage to diverse biomolecules, including lipids, proteins, DNA and carbohydrates (discussed below). [Pg.102]

Poli, G., Cheeseman, K.H., Biasi, F., Chiarpotto, E., Dianzani, M.U., Esterbauer, H. and Slater, T.F. (1989a). Promethazine inhibits the formation of aldehydic products of the lipid peroxidation that is stimulated by carbon tetrachloride, but does not inhibit covalent binding of metabolites of carbon tetrachloride to microsomal lipid protein. Biochem. J. 264, 527-532. [Pg.245]

To use liposomes as delivery systems, drug is added during the formation process. Flydrophilic compounds usually reside in the aqueous portion of the vesicle, whereas hydrophobic species tend to remain in the lipid proteins. The physical characteristics and stability of lipsomal preparations depend on pH, ionic strength, the presence of divalent cations, and the nature of the phospholipids and additives used [45 47],... [Pg.516]

Lipoproteins. A lipoprotein is an endogenous macromolecule consisting of an inner apolar core of cholesteryl esters and triglycerides surrounded by a monolayer of phospholipid embedded with cholesterol and apoproteins. The functions of lipoproteins are to transport lipids and to mediate lipid metabolism. There are four main types of lipoproteins (classified based on their flotation rates in salt solutions) chylomicrons, very-low-density lipoprotein (VLDL), low-density lipoprotein (LDL), and high-density lipoprotein (HDL). These differ in size, molecular weight, and density and have different lipid, protein, and apoprotein compositions (Table 11). The apoproteins are important determinants in the metabolism of lipoproteins—they serve as ligands for lipoprotein receptors and as mediators in lipoproteins interconversion by enzymes. [Pg.557]

Biological membranes consist of lipids, proteins and also sugars, sometimes mutually bonded in the form of lipoproteins, glycolipids and glycoproteins. They are highly hydrated—water forms up to 25 per cent of the dry weight of the membrane. The content of the various protein and lipid components varies with the type of biological membrane. Thus, in... [Pg.445]

Uittenbogaard, A, Everson, WV, Matveev, SV, and Smart, EJ, 2002. Cholesteryl ester is transported from caveolae to internal membranes as part of a caveolin-annexin II lipid-protein complex. J Biol Chem 277,4925—4-931. [Pg.352]

We must give first an outline of the non-metal pathways which we observe in all cells. We start here because we know nothing about their abiotic chemistry but assume that cellular life arose from it. We shall assume that the basic requirement of all metabolism is the energised and catalysed synthesis of polysaccharides, lipids, proteins and nucleic acids. These are polymers (see Table 4.5), formed from monomers, all of which could have always arisen when energy was applied to the... [Pg.138]


See other pages where Lipidated proteins is mentioned: [Pg.545]    [Pg.225]    [Pg.514]    [Pg.665]    [Pg.1026]    [Pg.253]    [Pg.691]    [Pg.1159]    [Pg.40]    [Pg.425]    [Pg.413]    [Pg.185]    [Pg.269]    [Pg.105]    [Pg.131]    [Pg.137]    [Pg.270]    [Pg.390]    [Pg.899]    [Pg.196]    [Pg.287]    [Pg.292]    [Pg.173]    [Pg.58]    [Pg.54]    [Pg.233]    [Pg.209]   
See also in sourсe #XX -- [ Pg.240 , Pg.245 ]




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Adipocyte lipid binding protein

Adipocyte lipid-binding protein difference

Adipocyte lipid-binding protein function

Adipocyte lipid-binding protein structure

Amyloid proteins lipid rafts

Arrangement of Lipids and Proteins in Sarcoplasmic Reticulum Membranes

Binding of Lipids to Proteins

Biomolecules Lipids Proteins

Bovine milk lipids major proteins

Brain lipid-binding protein

Catalysts Based on Hollow Lipid-binding Proteins

Chemistry, protein lipidation

Complex lipids, synthesis proteins

Complex systems lipid-protein mixtures and cell membranes

Composition of Thylakoid Membranes Lipids, Proteins, and Electron Carriers

Cytosolic lipid-protein particles

Edible protein-lipid

Glycosphingolipids lipid raft domains, proteins

Heme proteins lipid oxidation initiation

Hordeum lipid transfer proteins

Hordeum lipid transfer proteins endoproteinases

Ileal lipid-binding protein

Immune response lipid-binding proteins

Infectious proteins lipid rafts

Interaction between lipids and proteins

Keratinocyte lipid-binding proteins

Lipid Transfer Protein-I (LTP

Lipid acceptor protein

Lipid bilayers interaction with proteins

Lipid distributions, green protein

Lipid exchange proteins

Lipid interactions with dietary protein

Lipid interactions, transmembrane proteins

Lipid interfaces, protein

Lipid membranes proteins

Lipid oxidation protein hydrolysates

Lipid pathway, of protein glycosylation, and

Lipid peroxidation protein reactions with products

Lipid peroxidation reactivity with proteins

Lipid protein foam, stability

Lipid rafts protein

Lipid soluble protein

Lipid transfer proteins

Lipid-Binding Protein Cavity

Lipid-Protein Complexes

Lipid-assisted protein folding

Lipid-binding proteins

Lipid-binding proteins characterization

Lipid-binding proteins conformational similarity

Lipid-binding proteins crystallographic studies

Lipid-binding proteins cytoplasmic

Lipid-binding proteins difference

Lipid-binding proteins extracellular

Lipid-binding proteins function

Lipid-binding proteins homologies

Lipid-binding proteins intracellular

Lipid-binding proteins members

Lipid-binding proteins physiological functions

Lipid-binding proteins protein

Lipid-binding proteins protein folding

Lipid-binding proteins structural motif

Lipid-binding proteins types

Lipid-binding proteins water soluble

Lipid-dependent membrane protein

Lipid-protein bilayer membranes linked

Lipid-protein interactions amphiphiles, role

Lipid-protein interactions and rotational diffusion

Lipid-protein isolates

Lipid-protein particles

Lipid-protein—carbohydrate

Lipid/protein bilayer

Lipide-protein complex

Lipids and Proteins Are Associated in Biological Membranes

Lipids covalent links with proteins

Lipids fatty acid-binding proteins

Lipids food proteins, radical-induced

Lipids matrix, function membrane proteins

Lipids protein oxidation

Lipids protein systems

Lipids protein-bound

Lipids protein-lipid interactions

Lipids proteins

Lipids, protein interactions membranes

Lipoproteins lipid-protein interactions

Membrane lipid bilayers proteins

Membrane lipid bilayers reconstituted protein systems

Membrane lipid-protein interaction model

Membrane protein-tethered bilayer lipid membranes

Membrane proteins specific lipid requirement

Membranes protein:lipid ratio

Mitochondrial lipid-protein complexes

Modifications of Proteins—Glycosolation, Lipidation, Phosphorylation

Nonspecific lipid-transfer proteins

Organization of Lipids and Proteins in Lipophorins

Pathogenic proteins lipid-protein interactions

Peripheral membrane proteins lipid bilayer surface

Phosphatidylinositol lipid-dependent protein

Phosphoinositides protein lipid-binding domains

Plasma Lipid Transfer Proteins

Protein Lipidation

Protein crystallization lipidation

Protein lipid complex, disadvantages

Protein lipid-anchored

Protein lipidation patterns

Protein molecules with bound lipid

Protein to lipid ratio

Protein with lipid

Protein with lipids, interaction

Protein-lipid charge interactions

Protein-lipid edible films

Protein-lipid interactions atomic structure

Protein-lipid interactions selectivity

Protein-lipid respiratory chain complexes

Protein-lipid vesicles

Protein-tethered bilayer lipid membrane

Proteins interact with lipid rafts

Proteins lipid environment

Proteins lipid interactions

Proteins lipid peroxidation

Proteins lipid peroxidation aldehyde adducts

Proteins, Lipids, and Nucleic Acids

Proteins, changes during lipid oxidation

Proteins, chemical synthesis lipidation

Proteins, lipid transfer activity

Purified lipid transfer proteins

Semisynthesis of Lipidated LC3 Protein

Semisynthetic Lipidated LC3 Protein Mediates Membrane Fusion

Skill 12.1o-Recognize that inorganic and organic compounds (e.g., water, salt, carbohydrates, lipids, proteins, nucleic acids) are essential to processes within living systems

Transfer proteins microsomal lipid

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