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Phospholipases phospholipase

FIGURE 10-15 The specificities of phospholipases. Phospholipases Ai and A2 hydrolyze the ester bonds of intact glycerophospholipids at C-l and C-2 of glycerol, respectively. Phospholipases C and D each split one of the phosphodiester bonds in the head group. Some phospholipases act on only one type of glycerophospholipid, such as phosphatidylinositol 4,5-bisphosphate (shown here) or phosphatidylcholine others are less specific. When one of the fatty acids has been removed by a type A phospholipase, the second fatty acid is cleaved from the molecule by a lysophospholipase (not shown). [Pg.355]

Among the phospholipases, phospholipase A2 has been of major importance in establishing the positional specificity of fatty acids on the glycerophosphocholine backbone. However, two other phospholipases, namely C... [Pg.74]

Early studies were concerned with the anemia associated with trypanosomiasis, perhaps eaused by free fatty acids and lysophospholipids, as the products of phospholipases. Phospholipase A i is found in plasma and tissue fluids of infected animals and cleaves acyl chains from both exogenous lysophospholipids and PC, yielding both free fatty acids and 2-lysophosphatidylcholine. The latter lipid is then rearranged to a... [Pg.141]

Hydrolases. Enzymes catalysing the hydrolytic cleavage ofC —O, C —N and C —C bonds. The systematic name always includes hydrolase but the recommended name is often formed by the addition of ase to the substrate. Examples are esterases, glucosidases, peptidases, proteinases, phospholipases. Other bonds may be cleaved besides those cited, e.g. during the action of sulphatases and phosphatases. [Pg.159]

Although extraction of lipids from membranes can be induced in atomic force apparatus (Leckband et al., 1994) and biomembrane force probe (Evans et al., 1991) experiments, spontaneous dissociation of a lipid from a membrane occurs very rarely because it involves an energy barrier of about 20 kcal/mol (Cevc and Marsh, 1987). However, lipids are known to be extracted from membranes by various enzymes. One such enzyme is phospholipase A2 (PLA2), which complexes with membrane surfaces, destabilizes a phospholipid, extracts it from the membrane, and catalyzes the hydrolysis reaction of the srir2-acyl chain of the lipid, producing lysophospholipids and fatty acids (Slotboom et al., 1982 Dennis, 1983 Jain et al., 1995). SMD simulations were employed to investigate the extraction of a lipid molecule from a DLPE monolayer by human synovial PLA2 (see Eig. 6b), and to compare this process to the extraction of a lipid from a lipid monolayer into the aqueous phase (Stepaniants et al., 1997). [Pg.50]

Ferguson, K.M., et al. Structure of the high affinity complex of inositol triphosphate with a phospholipase C pleckstrin homology domain. Celt 83 1037-1046, 1995. [Pg.280]

Pseudopterosin A is a member of a group of marine natural products which show potent antiinflammatory properties, but which are not prostaglandin biosynthesis inhibitors. Structurally similar to phosphatidyl inositol, they may function as phospholipase inhibitors, and, as such, may be the forerunners of a new class of therapeutic agents. [Pg.237]

Hydrolytic enzymes phospholipases in snake venoms, endogenous... [Pg.286]

Phosphatidylcholine Apply phospholipase C solution as a band, dry, apply sample solution to enzyme band, stop reaction with hydrochloric acid vapor. sn-l,2-Digly-cerides are produced. [43]... [Pg.64]

The venoms of poisonous snakes contain (among other things) a class of enzymes known as phospholipases, enzymes that cause the breakdown of phospholipids. For example, the venoms of the eastern diamondback rattlesnake (Crotalus adamanteus) and the Indian cobra Naja naja) both contain phospholipase Ag, which catalyzes the hydrolysis of fatty acids at the C-2 position of glyc-erophospholipids. [Pg.246]

Eicosanoids, so named because they are all derived from 20-carbon fatty acids, are ubiquitous breakdown products of phospholipids. In response to appropriate stimuli, cells activate the breakdown of selected phospholipids (Figure 25.27). Phospholipase Ag (Chapter 8) selectively cleaves fatty acids from the C-2 position of phospholipids. Often these are unsaturated fatty acids, among which is arachidonic acid. Arachidonic acid may also be released from phospholipids by the combined actions of phospholipase C (which yields diacyl-glycerols) and diacylglycerol lipase (which releases fatty acids). [Pg.829]

LY311727 is an indole acetic acid based selective inhibitor of human non-pancreatic secretory phospholipase A2 (hnpsPLA2) under development by Lilly as a potential treatment for sepsis. The synthesis of LY311727 involved a Nenitzescu indolization reaction as a key step. The Nenitzescu condensation of quinone 4 with the p-aminoacrylate 39 was carried out in CH3NO2 to provide the desired 5-hydroxylindole 40 in 83% yield. Protection of the 5-hydroxyl moiety in indole 40 was accomplished in H2O under phase transfer conditions in 80% yield. Lithium aluminum hydride mediated reduction of the ester functional group in 41 provided the alcohol 42 in 78% yield. [Pg.150]

FIGURE 2.7 Production of second messengers inositol 1,4,5-triphosphate (IP3) and diacylglycerol (DAG) through activation of the enzyme phospholipase C. This enzyme is activated by the a- subunit of Gq-protein and also by Py subunits of Gj-protein. IP3 stimulates the release of Ca2+ from intracellular stores while DAG is a potent activator of protein kinase C. [Pg.25]

Phospholipase C, 24 pK0, 125, 144-145 Polar metabolites, 165 Polymorphisms, 4 Polypharmacology, 190-192 Pooled variance, 228 Populations, 226-228, 232 Positive agonism, 49 Potency... [Pg.297]

The second type of material includes spores, which may or may not produce disease symptoms but which can germinate in the insect gut and give rise to vegetative bacterial cells which in turn may produce, and exoenzymes such as phospholipases (lecithinases) or hyaluronidase. The phospholipases may produce direct toxic symptoms owing to their action on nervous or other phospholipid-containing tissue. Hyaluronidase breaks down hyaluronic acid and produces effects on animal tissue which are morphologically similar to the breakdown of insect gut wall in the presence of microbial insecticide preparations. [Pg.71]

Heat-labile soluble toxin Exoenzymes (phospholipases, hyaluronidase) Vegetative bacterial cells... [Pg.79]

PH domains consist of about 120 amino acid residues. They do not interact with other proteins, but associate with specific polyphosphoinositides. Consequently, PH domains appear to be important for localizing target proteins to the plasma membrane. Examples of PH domain-containing proteins include phospholipase C andpl20/RasGAP (Fig. 1). [Pg.18]

Two AR subtypes, Ax and A3, couple through G to inhibit adenylate cyclase, while the other two subtypes, A2a and A2B, stimulate adenylate cyclase through Gs or G0if (for A2a). The A2BAR is also coupled to the activation of PLC through Gq. Furthermore, each of these receptors may couple through the (3,y subunits of the G proteins to other effector systems, including ion channels and phospholipases. Levels of intracellular... [Pg.22]

TXA2 is produced by activated platelets via the sequential conversion of arachidonic acid by phospholipase A2, cyclooxygenase-1 (COX-1), and thromboxane synthase. Similar to ADP, TXA2 acts as a... [Pg.167]

Pasteurella multocida toxin (PMT) is the major pathogenic factor responsible for atrophic rhinitis, a disease which is characterized by bone loss in the nose of pigs. PMT is a 145 kDa single-chain exotoxin, which activates Goq protein (but not Gan) and stimulates phospholipase C 3. In addition, G12/i3 proteins and subsequently Rho pathways are activated. [Pg.247]


See other pages where Phospholipases phospholipase is mentioned: [Pg.248]    [Pg.408]    [Pg.10]    [Pg.225]    [Pg.240]    [Pg.307]    [Pg.547]    [Pg.17]    [Pg.43]    [Pg.51]    [Pg.61]    [Pg.62]    [Pg.64]    [Pg.278]    [Pg.278]    [Pg.72]    [Pg.252]    [Pg.271]    [Pg.279]    [Pg.286]    [Pg.189]    [Pg.24]    [Pg.98]    [Pg.78]    [Pg.78]    [Pg.79]    [Pg.44]    [Pg.44]    [Pg.44]    [Pg.169]    [Pg.247]    [Pg.247]    [Pg.274]    [Pg.282]    [Pg.297]    [Pg.302]   
See also in sourсe #XX -- [ Pg.2 , Pg.268 ]

See also in sourсe #XX -- [ Pg.358 , Pg.382 ]




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Acetylcholine phospholipase

Amino acid phospholipase

Angiotensin phospholipase

Bacillus cereus, phospholipase

Bacterial phospholipase C

Brain phospholipid metabolism phospholipase

Cabbage phospholipase

Calcium phospholipase

Calcium phospholipases

Calcium, secretory phospholipase

Castor bean phospholipase

Catalysis of Secretory Phospholipases

Cellular phospholipases

Cirsium japonicum DC, phospholipase inhibition

Clostridium perfringens phospholipase

Cobra venom phospholipase

Crotalus adamanteus venom, phospholipase

Eicosanoids phospholipases

Enzymes phospholipase

Escherichia coli phospholipases

Extracellular phospholipases

Fatty acid phospholipase

G-proteins phospholipase

GPI-specific phospholipase D

Glycosyl phosphatidylinositol phospholipase

Heart disease phospholipase

Helices phospholipases

Histamine Phospholipase

Hydrolysis phospholipase

Hydrolysis with phospholipase

Immobilization phospholipase

Independent Phospholipase

Inflammation Phospholipase

Inositol 1,4,5-trisphosphate phospholipase

Inositol phospholipids phospholipase

Insulin phospholipase

Lipase phospholipase

Lipases, Esterases, and Phospholipases

Lipids phospholipases

Liposome phospholipase

Lipoxygenase and Phospholipase

Mammalian phospholipase C

Markers phospholipase

Membrane phospholipase

Modulation of Insulin Secretion via Adenylate Cyclase and Phospholipase C (PLC)

Molecular phospholipase

Nuclear magnetic resonance phospholipase

PLC (phospholipase

PLC, Phospholipase C

Pancreas phospholipase

Pancreatin phospholipase

Penicillium phospholipase

Phenol phospholipase

Phosphatidylinositol Phospholipase C (PI-PLC)

Phosphatidylinositol phospholipase

Phosphatidylinositol-specific phospholipase

Phosphoinositides Phospholipases

Phospholipase

Phospholipase

Phospholipase , general

Phospholipase 13 pathways

Phospholipase A

Phospholipase A, (PLA

Phospholipase A, enzyme

Phospholipase A-.., hydrolysis

Phospholipase A2 Activity

Phospholipase A2 complexes

Phospholipase A2 enzyme

Phospholipase A2 inhibition

Phospholipase A2 inhibitors

Phospholipase Action

Phospholipase Assays Using Conjugated Polyelectrolytes

Phospholipase B and

Phospholipase C

Phospholipase C . See

Phospholipase C activity

Phospholipase C and

Phospholipase C enzyme

Phospholipase C gamma

Phospholipase C inhibitors

Phospholipase C, hydrolysis

Phospholipase C-y

Phospholipase C. activation

Phospholipase C/DAG

Phospholipase Classification

Phospholipase D

Phospholipase D enzyme

Phospholipase Reaction

Phospholipase Regulation

Phospholipase Subfamilies

Phospholipase Subject

Phospholipase a, occurrence and phosphatidyl ethanolamine

Phospholipase a, occurrence and phosphatidyl glycerol

Phospholipase activation

Phospholipase activators

Phospholipase activity

Phospholipase activity effect

Phospholipase activity leaves

Phospholipase amino acid sequence

Phospholipase aminoglycosides

Phospholipase arachidonic acid release

Phospholipase assays

Phospholipase binding

Phospholipase biological tissue

Phospholipase catalysis

Phospholipase catalytic activity modulated

Phospholipase catalytic mechanism

Phospholipase cation requirements

Phospholipase characteristics

Phospholipase definition

Phospholipase design

Phospholipase glycerophospholipids

Phospholipase hydrolysis, products

Phospholipase incubation conditions

Phospholipase inflammation mediation

Phospholipase inhibition

Phospholipase inhibitors

Phospholipase injection

Phospholipase isoforms

Phospholipase isolation and purification

Phospholipase isozyme

Phospholipase isozymes

Phospholipase leaves

Phospholipase mechanisms

Phospholipase membrane binding

Phospholipase microsome preparation

Phospholipase molecular weight

Phospholipase occurrence

Phospholipase overview

Phospholipase peptides

Phospholipase phosphatidylglycerol

Phospholipase phosphodiesterase activity

Phospholipase phosphoinositide-specific

Phospholipase phospholipid degradation

Phospholipase physiological role

Phospholipase physiological’ effects

Phospholipase platelet metabolism

Phospholipase properties

Phospholipase prostaglandins

Phospholipase solutions

Phospholipase sources

Phospholipase specificity

Phospholipase structure

Phospholipase substrate preference

Phospholipase substrate preparation

Phospholipase substrate specificity

Phospholipase substrates

Phospholipase synthesis

Phospholipase transphosphatidylation reaction

Phospholipase venom

Phospholipase, Plasma

Phospholipase, cereal

Phospholipase, domain structure

Phospholipase, hormone sensitive

Phospholipase-vesicle interaction

Phospholipases

Phospholipases

Phospholipases A

Phospholipases A, (PLA

Phospholipases A2 An Overview

Phospholipases B

Phospholipases C

Phospholipases Degrade Phospholipids

Phospholipases activation

Phospholipases and

Phospholipases assay

Phospholipases bacterial

Phospholipases bilayer

Phospholipases classification

Phospholipases defined

Phospholipases degradation

Phospholipases dependence

Phospholipases enzymes

Phospholipases fungal

Phospholipases plant

Phospholipases remodeling

Phospholipases transfer protein

Phospholipases turnover

Phospholipases, control

Phospholipases, control proteins

Phospholipases, eicosanoids synthesi

Phospholipases, lipoprotein degradation

Phospholipases, other

Phospholipases, snake venom

Phospholipases/lipases

Phospholipids, phospholipase

Phospholipids, phospholipase hydrolysis

Platelet activating factor phospholipases

Platelet activation phospholipases

Polarized residues phospholipase

Protein phospholipase

Proteins that Modulate Phospholipase A2 Activity

Resistance to phospholipases

Roles of Phospholipases in Response to Freezing

Secreted phospholipases enzymes

Secreted phospholipases enzymes group

Secreted phospholipases enzymes other

Secretory phospholipase

Secretory phospholipase inhibitor

Signal transduction phospholipase

Signal transduction phospholipases

Signaling phospholipase

Snake venoms phospholipase

Soluble phospholipases

Structure and Catalytic Mechanism of Mammalian Phospholipase

Substrate availability phospholipases

Synaptic transmission, phospholipase

Synovial phospholipase

Vitamin D (cont phospholipase

Water interface, phospholipase

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