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9783527306770

Lipases and Phospholipases in Drug Development: From Biochemistry to Molecular Pharmacology

by ;
  • ISBN13:

    9783527306770

  • ISBN10:

    3527306773

  • Edition: 1st
  • Format: Hardcover
  • Copyright: 2004-04-01
  • Publisher: VCH PUBLISHER INC

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Summary

Lipases and Phospholipases are key control elements in mammalian metabolism. They share many common features that set them apart from other metabolic enzyme classes, most importantly their association with biological membranes. Their potential as drug targets for the treatment of metabolic diseases is widely recognized, and the first lipase inhibitor drugs have been successfully introduced. Providing drug developers with a firm foundation for lipase-centered drug design, the editors of this volume have assembled experts from different scientific disciplines to create a comprehensive handbook for all pharmaceutical chemists, biochemists and physiologists working with lipases. The authors examine fundamental aspects of lipase function in vitro and in vivo, explaining how this knowledge may be used to develop lipase assays. They also treat the physiological roles of lipases in normal and disordered metabolism, as well as strategies to target lipases for the treatment of diabetes, obesity and related disorders. Additional topics include the application of phospholipases for liposome-based drug delivery and their use as diagnostic tools.

Author Biography

<b>G&#252;nter M&#252;ller</b> is senior scientist for Biochemistry at Aventis Pharma Germany, Frankfurt am Main, and honorary lecturer for genetics at the University of Munich. He was born in Peissenberg (Germany) and studied anthropology, zoology, genetics and biochemistry at the Ludwig-Maximilians-University in Munich, finishing his PhD thesis under the supervision of R. Zimmermann in 1987. After post-doctoral fellowships at the universities of Ulm and Heidelberg, he joined the pharmaceutical industry in 1990 and received his habilitation at the University of Munich in 1996. He is interested in molecular mechanisms in both lower eukaryotes and mammalian cells, and their use as drug targets for metabolic disorder. <p> <b>Stefan Petry</b> is senior scientist in Medicinal Chemistry at Aventis Germany, Frankfurt am Main. He was born in Kaiserslautern (Germany) and studied Chemistry and Biochemistry at the Albert-Ludwigs-University in Freiburg, including his PhD thesis under the supervision of Jochen Lehmann on photo-affinity labeling of carbohydrate binding proteins. He joined the pharmaceutical industry in 1994. At Aventis he is responsible for projects in the field of diabetes. In particular, he is interested in the development of small molecules which interact with signal transduction processes or influence lipid metabolism.

Table of Contents

Preface xiii
List of Contributors xv
1 Purification of Lipase
1(22)
Palligarnai T. Vasudevan
1.1 Introduction
2(1)
1.2 Pre-purification Steps
2(1)
1.3 Chromatographic Steps
3(4)
1.4 Unique Purification Strategies
7(2)
1.5 Theoretical Modeling
9(10)
1.5.1 Model Formulation
9(1)
1.5.1.1 Mobile Phase
9(1)
1.5.1.2 Stationary Phase
10(1)
1.5.1.3 Boundary Conditions
10(1)
1.5.2 Solution
11(2)
1.5.3 Method of Moments
13(2)
1.5.4 Model Evaluation
15(1)
1.5.5 Simulation Results
16(1)
1.5.5.1 Effect of Feed Angle
16(1)
1.5.5.2 Effect of Flow Rate
17(1)
1.5.5.3 Effect of Rotation Rate
17(1)
1.5.5.4 Effect of Column Height
19(1)
1.6 Conclusions
19(1)
1.7 Acknowledgements
20(1)
1.8 References
20(3)
2 Phospholipase A1 Structures, Physiological and Patho-physiological Roles in Mammals
23(18)
Keizo Inoue, Hiroyuki Arai, and Junken Aoki
2.1 Introduction
23(4)
2.2 Phosphatidylserine-specific Phospholipase Al (PS-PLA1)
27(5)
2.2.1 Historical Aspects
27(1)
2.2.2 Biochemical Characterization and Tissue Distribution
27(2)
2.2.3 Structural Characteristics
29(1)
2.2.4 Substrate Specificity
29(1)
2.2.5 Possible Functions
30(2)
2.3 Membrane-associated Phosphatidic Acid-selective Phospholipase A1s (mPA-PLA1α and mPA-PLA1β)
32(3)
2.3.1 Historical Aspects
32(1)
2.3.2 Characterization and Distribution
33(1)
2.3.3 Structural Characteristics
34(1)
2.3.4 Function
34(1)
2.4 Phosphatidic Acid-preferring Phospholipase Al (PA-PLA1)
35(2)
2.4.1 Historical Aspects
35(1)
2.4.2 Characterization and Distribution
36(1)
2.4.3 Substrate Specificity
36(1)
2.4.4 Function
37(1)
2.5 KIAA0725P, a Novel PLA1 with Sequence Homology to a Mammalian Sec23p-interacting Protein, p125
37(1)
2.5.1 Historical Aspects
37(1)
2.5.2 Characterization and Distribution
37(1)
2.6 References
38(3)
3 Rational Design of a Liposomal Drug Delivery System Based on Biophysical Studies of Phospholipase A2 Activity on Model Lipid Membranes
41(14)
Kent Jørgensen, Jesper Davidsen, Thomas L. Andresen, and Ole G. Mouritsen
3.1 Introduction
41(2)
3.2 Role for Secretory Phospholipase A2 (sPLA2) in Liposomal Drug Delivery
43(1)
3.3 Lateral Microstructure of Lipid Bilayers and its Influence on sPLA2
43(3)
3.4 sPLA2 Degradation of Drug-delivery Liposomes: A New Drug-delivery Principle
46(5)
3.4.1 Liposomes Protected by Polymer Coating
46(1)
3.4.2 Biophysical Model Drug-delivery System to Study sPLA2 Activity
47(1)
3.4.3 Effect of Lipid Composition on sPLA2-triggered Drug Release and Absorption
48(1)
3.4.4 Effect of Temperature on Liposomal Drug Release and Absorption by sPLA2
49(1)
3.4.5 Liposomal Drug Release as a Function of sPLA2 Concentration
50(1)
3.5 Conclusion
51(1)
3.6 Acknowledgments
51(1)
3.7 References
52(3)
4 Phospholipase D
55(24)
John H. Exton
4.1 Introduction
55(1)
4.2 Structure and Catalytic Mechanism of Mammalian Phospholipase D
56(2)
4.3 Cellular Locations of PLD1 and PLD2
58(1)
4.4 Post-translational Modification of PLD
59(1)
4.5 Regulation of PLD1 and PLD2
60(4)
4.5.1 Role of PIP2
60(1)
4.5.2 Role of PKC
61(3)
4.6 Role of Rho Family GTPases
64(1)
4.7 Role of Arf Family GTPases
65(1)
4.8 Role of Tyrosine Kinase
66(1)
4.9 Role of Ral
66(1)
4.10 Cellular Functions of PLD
66(1)
4.11 Role of PLD in Growth and Differentiation
67(1)
4.12 Role of PLD in Vesicle Trafficking in Golgi
68(1)
4.13 Role of PLD in Exocytosis and Endocytosis
68(1)
4.14 Role of PLD in Superoxide Formation
69(1)
4.15 Role in Actin Cytoskeleton Rearrangements
70(1)
4.16 Role in Lysophosphatidic Acid Formation
71(1)
4.17 Role of PA in Other Cellular Systems
71(1)
4.18 References
72(7)
5 Sphingomyelinases and Their Interaction with Membrane Lipids
79(22)
Félix M. Goñi and Alicia Alonso
5.1 Introduction and Scope
5.2 Sphingomyelinases
80(9)
5.2.1 Types of Sphingomyelinases
80(1)
5.2.1.1 Acid Sphingomyelinase (aSMase)
80(1)
5.2.1.2 Secretory Sphingomyelinase (sSMase)
81(1)
5.2.1.3 Neutral, Mg²+-dependent Sphingomyelinases (nSMase)
81(1)
5.2.1.4 Mg²-independent Neutral Sphingomyelinases
84(1)
5.2.1.5 Alkaline Sphingomyelinase from the Intestinal Tract
85(1)
5.2.1.6 Bacterial Sphingomyelinase-phospholipase C
85(1)
5.2.2 Sphingomyelinase Mechanism
85(1)
5.2.2.1 Binding of Magnesium Ions
85(1)
5.2.2.2 Binding of Substrate
85(1)
5.2.2.3 Mechanism of Catalysis
86(2)
5.2.3 Sphingomyelinase Assay
88(1)
5.2.4 Sphingomyelinase Inhibitors
89(1)
5.3 Sphingomyelinase-Membrane Interactions
89(7)
5.3.1 Lipid Effects on Sphingomyelinase Activity
90(1)
5.3.2 Effects of Sphingomyelinase Activity on Membrane Properties
91(1)
5.3.2.1 Effects on Membrane Lateral Organization
91(1)
5.3.2.2 Effects on Membrane Permeability
93(1)
5.3.2.3 Effects on Membrane Aggregation and Fusion
94(2)
5.4 Acknowledgments
96(1)
5.5 References
96(5)
6 Glycosyl-phosphatidylinositol Cleavage Products in Signal Transduction
101(20)
Yolanda Leon and Isabel Varela-Nieto
6.1 Introduction
101(1)
6.2 GPI Structure and Hydrolysis by Specific Phospholipases
102(2)
6.3 Diffusible Factors and the Regulation of GPI Levels
104(2)
6.4 IPG Structure and Biological Activities
106(3)
6.5 GPI/IPG Pathway and the Intracellular Signaling Circuit
109(3)
6.6 Acknowledgments
112(1)
6.7 References
113(8)
7 High-throughput Screening of Hormone-sensitive Lipase and Subsequent Computer-assisted Compound Optimization
121(18)
Stefan Petry, Karl-Heinz Baringhaus, Karl Schoenafinger, Christian Jung, Horst Kleine, and Günter Müller
7.1 Introduction
121(1)
7.1.1 Lipases in Metabolism
121(1)
7.2 Lipases Show Unique Differences in Comparison to Other Drug Targets
122(1)
7.3 Lipase Assays
123(2)
7.4 Hormone-sensitive Lipase (HSL) as a Drug Target in Diabetes
125(9)
7.4.1 Biological Role of HSL
125(1)
7.4.2 Characteristics of HSL
126(2)
7.4.3 Inhibitors of HSL
128(6)
7.5 Perspective
134(1)
7.6 References
134(5)
8 Endothelial Lipase: A Novel Drug Target for HDL and Atherosclerosis?
139(16)
Karen Badellino, Weijun Jin, and Daniel J. Rader
8.1 Introduction
139(1)
8.2 Structure of Endothelial Lipase
140(1)
8.3 Tissue Expression of Endothelial Lipase and Its Implications
141(1)
8.4 Enzymatic Activity and Effects on Cellular Lipid Metabolism of Endothelial Lipase
142(3)
8.5 Regulation of Endothelial Lipase Expression
145(1)
8.6 Physiology of Endothelial Lipase
146(3)
8.7 Variation in the Human Endothelial Lipase Gene
149(2)
8.8 Endothelial Lipase as a Potential Pharmacologic Target
151(1)
8.9 References
151(4)
9 Digestive Lipases Inhibition: an In vitro Study
155(40)
Ali Tiss, Nabil Miled, Robert Verger, Youssef Gargouri, and Abdelkarim Abousalham
9.1 Introduction
155(4)
9.1.1 3-D Structure of Human Pancreatic Lipase
156(2)
9.1.2 3-D Structure of Human Gastric Lipase
158(1)
9.2 Methods for Lipase Inhibition
159(5)
9.2.1 Method A: Lipase/Inhibitor Pre-incubation
162(1)
9.2.2 Method B: Inhibition During Lipolysis
162(1)
9.2.3 "Pre-poisoned" Interfaces
163(1)
9.2.3.1 Method C
163(1)
9.2.3.2 Method D
163(1)
9.3 Inhibition of Lipases by E600 and Various Phosphonates
164(23)
9.3.1 Inhibition of PPL, HGL and RGL by Radiolabcled E600
165(2)
9.3.2 Interfacial Binding to Tributyrin Emulsion of Native and Chemically Modified Digestive Lipases
167(1)
9.3.3 Inhibition of Lipases by Phosphonates and the 3-D Structures of Lipase-inhibitor Complexes
167(1)
9.3.3.1 Synthesis of New Chiral Organophosphorus Compounds Analogous to TAG
167(1)
9.3.3.2 The 2.46 Å Resolution Structure of the Pancreatic/Procolipase Complex Inhibited by a C11 Alkylphosphonate
170(1)
9.3.3.3 tive Lipases by Orlistat
174(1)
9.4.1 Introduction
174(1)
9.4.2 Inhibition of Digestive Lipases by Pre-incubation with Orlistat (Method A)
175(1)
9.4.2.1 Inhibition of Gastric Lipases
175(1)
9.4.2.2 Inhibition of Pancreatic Lipases
176(1)
9.4.2.3 Kinetic Model Illustrating the Covalent Inhibition of HPL in the Aqueous Phase
180(1)
9.4.3 Inhibition of Digestive Lipases During Lipolysis (Method B)
181(1)
9.4.4 Inhibition of Digestive Lipases on Oil Emulsions "Poisoned" with Orlistat (Method C)
181(3)
9.4.5 Inhibition of Digestive Lipases on Oil Substrate "Poisoned" with Orlistat (Method D)
184(1)
9.4.5.1 Inhibition of Pancreatic Lipase on Emulsion "Pre-poisoned" with Orlistat
184(1)
9.4.5.2 Inhibition of Gastric and Pancreatic Lipases on Mixed Films Containing Orlistat
185(1)
9.4.5.3 Inhibition of Pancreatic Lipase on Oil Drop "Pre-poisoned" with Orlistat
185(2)
9.5 References
187(8)
10 Physiology of Gastrointestinal Lipolysis and Therapeutical Use of Lipases and Digestive Lipase Inhibitors 195(36)
Hans Lengsfeld, Gabrielle Beaumier-Gallon, Henri Chahinian, Alain De Caro, Robert Verger, Rene Laugier, and Frédéric Carrière
10.1 Introduction
195(1)
10.2 Tissular and Cellular Origins of HGL and HPL
196(1)
10.3 Hydrolysis of Acylglycerols by HGL and HPL
199(1)
10.3.1 Substrate Specificity
199(1)
10.3.2 Specific Activities of HGL and HPL
200(2)
10.3.3 Lipase Activity as a Function of pH
202(1)
10.3.4 Effects of Bile Salts on the Activity of HGL and HPL
202(2)
10.4 Gastrointestinal Lipolysis of Test Meals in Healthy Human Volunteers
204(1)
10.4.1 Test Meals
205(2)
10.4.2 Experimental Device for Collecting Samples in vivo
207(1)
10.4.3 Gastric and Duodenal pH Variations
207(1)
10.4.4 Lipase Concentrations and Outputs
207(4)
10.4.5 Lipolysis Levels
211(2)
10.5 HGL and HPL Stability
213(1)
10.6 Potential Use of Gastric Lipase in the Treatment of Pancreatic Insufficiency
215(1)
10.7 Inhibition of Gastrointestinal Lipolysis by Orlistat for Obesity Treatment
216(1)
10.7.1 The Lipase Inhibitor Orlistat
216(1)
10.7.2 Design of Clinical Studies for Quantification of Lipase and Lipolysis Inhibition
217(1)
10.7.3 HGL Inhibition by Orlistat
218(1)
10.7.4 HPL Inhibition by Orlistat
219(1)
10.7.5 Effects of Orlistat on Gastric Lipolysis
220(1)
10.7.6 Effects of Orlistat on Duodenal Lipolysis
221(1)
10.7.7 Effects of Orlistat on Overall Lipolysis
221(1)
10.7.8 Effects of Orlistat on Fat Excretion
221(1)
10.7.9 Weight Management by Orlistat in Obese Patients
222(2)
10.7.10 Conclusions
224(1)
10.8 References
224(7)
11 Physiological and Pharmacological Regulation of Triacylglycerol Storage and Mobilization 231(102)
Günter Müller
11.1 Metabolic Role of Triacylglycerol
231(1)
11.1.1 Triacylglycerol and Energy Storage
231(3)
11.1.2 Lipolysis and Re-esterification
234(2)
11.1.3 TAG Storage/Mobilization and Disease
236(1)
11.1.3.1 Diabetes Mellitus and Metabolic Syndrome
236(2)
11.1.3.2 Lipotoxicity
238(1)
11.1.3.2.1 β-Cells
238(1)
11.1.3.2.2 Cardiac Myocytes
239(1)
11.1.3.2.3 Molecular Mechanisms
240(1)
11.1.3.3 Inborn Errors of TAG Storage and Metabolism
241(1)
11.2 Components for TAG Storage and Mobilization
242(1)
11.2.1 TAG in lipoproteins
242(1)
11.2.2 TAG in Adipose Cells
243(1)
11.2.2.1 Enzymes of TAG Synthesis
244(2)
11.2.2.2 Lipid Droplets
246(1)
11.2.2.2.1 Morphology and Lipid Composition
246(2)
11.2.2.2.2 Protein Composition
248(4)
11.2.2.2.3 Biogenesis
252(7)
11.3 Mechanism and Regulation of TAG Mobilization
259(1)
11.3.1 cAMP
259(1)
11.3.2 Phosphorylation of HSL
260(3)
11.3.3 Dephosphorylation of HSL
263(1)
11.3.4 Intrinsic HSL Activity
263(1)
11.3.5 Translocation of HSL
264(1)
11.3.5.1 Mechanism
264(2)
11.3.5.2 Involvement of Perilipins
266(2)
11.3.5.3 Involvement of Lipotransin
268(2)
11.3.6 Intrinsic Activity of HSL
270(1)
11.3.6.1 Feedback Inhibition
270(2)
11.3.6.2 Adipocyte Lipid-binding Protein
272(2)
11.3.7 Expression of HSL
274(1)
11.3.8 Release of Lipolytic Products
275(1)
11.3.8.1 FA Transport
275(1)
11.3.8.2 Glycerol Transport
276(1)
11.3.8.3 Cholesterol Transport
277(1)
11.4 Physiological, Pharmacological and Genetic Modulation of TAG Mobilization
278(1)
11.4.1 Muscle Contraction
278(1)
11.4.2 Nutritional State
279(1)
11.4.3 Hormones and Cytokines
279(1)
11.4.3.1 Insulin
279(1)
11.4.3.1.1 Molecular Mechanisms
279(2)
11.4.3.1.2 Desensitization
281(1)
11.4.3.2 Leptin
282(1)
11.4.3.3 Growth Hormone
283(1)
11.4.3.4 Glucose-dependent Insulinotropic Polypeptide
283(1)
11.4.3.5 TNF-α
283(2)
11.4.4 ASP
285(1)
11.4.5 Acipimox and Nicotinic Acid
286(1)
11.4.5.1 Mode of Action
287(1)
11.4.5.2 Molecular Mechanism
288(1)
11.4.5.3 Desensitization
289(1)
11.4.6 Glimepiride and Phosphoinositolglycans
290(2)
11.4.7 Differences in Regulation of TAG Storage and Mobilization between Visceral and Subcutaneous Adipocytes
292(2)
11.4.8 Up-/Down-regulation of Components of TAG Storage and Mobilization
294(1)
11.4.8.1 HSL
294(2)
11.4.8.2 ALBP
296(1)
11.4.8.3 Perilipin
297(2)
11.4.8.4 PKA
299(1)
11.4.8.5 ASP
300(1)
11.4.8.6 Caveolin
301(1)
11.5 Concluding Remarks
302(1)
11.6 References
303(30)
Subject Index 333

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