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9780199636471

Growth Factors and Receptors A Practical Approach

by ;
  • ISBN13:

    9780199636471

  • ISBN10:

    0199636478

  • Format: Hardcover
  • Copyright: 1998-10-29
  • Publisher: Oxford University Press
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Summary

Growth Factors and Receptors provides comprehensive protocols for studiesof growth factors and their interactions with receptors. It covers a wide rangefrom simple analytical techniques to sophisticated in vivo applicationsincluding: RT-PCR and immunocytochemistry for detection of growth factors andreceptors; production and purification of recombinant growth factors andreceptors; labelling of growth factors for binding studies; in vivo mutagenesis;the yeast two-hybrid assay of protein/protein interactions; phage display offactors; application of factors to wound-healing processes using the gene gun;treatment of cancers with factor/toxin chimeras; and analysis of importantfactor domains using chimeric proteins. This book updates and extends thecurrent literature and describes important novel approaches to the study ofgrowth factors and their receptors, including the use of RNA aptamers asreceptor antagonists, and the development of receptor superantagonists. It willbe of tremendous value to both researchers and teachers, and, through anappendix that lists a large number of growth factors and receptors, will serveas a handy reference text.

Table of Contents

List of contributors
xvii
Abbreviations xxi
Engineered growth factors and receptors, and their applications
1(18)
Ian A. McKay
Stephen A. Bustin
Kenneth D. Brown
Introduction
1(1)
Known growth factors and receptors
1(1)
Modes of factor-receptor interaction
1(1)
Applications of engineered growth factors and receptors
2(1)
Principal methods for engineering growth factors and their receptors
2(2)
Mutagenesis
2(1)
Formation of chimeric proteins
3(1)
Manufacture of alternative ligands and receptors
3(1)
Design of engineered growth factors and receptors
4(3)
DNA sequence of factor or receptor to be engineered
4(1)
Analysis of existing DNA sequence for useful restriction sites
4(1)
Design of wholly synthetic growth factors and receptors
4(3)
Expression of DNAs encoding growth factors or receptors
7(12)
Deciding on an expression system
7(2)
Microbial expression
9(1)
In vitro expression
10(1)
Eukaryotic gene expression
11(6)
Acknowledgements
17(1)
References
17(2)
Engineering of novel neurotrophins
19(32)
Leopold L. Ilag
Carlos F. Ibanez
Introduction
19(1)
Structure-function analyses of neurotrophins
20(1)
Site-directed mutagenesis
21(6)
Kunkel method
22(4)
PCR-based mutagenesis
26(1)
Expression of recombinant protein
27(4)
COS cell expression
27(2)
Baculovirus expression
29(1)
Expression of recombinant proteins in prokaryotic systems (E. coli)
30(1)
Protein purification
31(2)
Biochemical assays
33(6)
Binding assay
33(3)
Cross-linking assay
36(1)
Phosphorylation assay
37(2)
Biological assays
39(6)
Therapeutic potential of engineered neurotrophins
45(1)
Conclusion
46(5)
Acknowledgements
47(1)
References
47(4)
Designing new agonists/antagonists of growth factor receptors-the rational design of a superantagonist of the IL-6 receptor
51(32)
G. Ciliberto
A. Lahm
G. Paonessa
R. Savino
C. Toniatti
Introduction
51(2)
Molecular modelling of a trimeric IL-6/IL-6Rα/gp130 complex
53(1)
Model construction
53(1)
Identification of the putative IL-6 site 1 and site 2 epitopes
53(1)
IL-6 biological assay
54(4)
In vitro binding assay of IL-6 to IL-6Rα
58(2)
IL-6 antagonists mutated in site 2: biochemical and biological evaluation
60(5)
Generation of IL-6 antagonists
61(2)
Specificity of IL-6 antagonists
63(2)
Tag-mediated immunoprecipitation assay (TAMIA)
65(4)
Selection of amino acid substitutions which increase affinity of IL-6 for IL-6Rα
69(8)
Generation of IL-6 phage particles
69(3)
Generation of IL-6 phage libraries
72(2)
Selection of IL-6 superbinders from a phage library
74(1)
IL-6 variants with higher affinity for IL-6Rα
75(2)
Combination of antagonistic and superbinder mutations to generate IL-6 superantagonists
77(1)
Potential use of IL-6 superantagonists in therapy
78(5)
Acknowledgements
79(1)
References
79(4)
A chimeric approach for studying receptor binding domains in EGF-like molecules
83(26)
E. J. J. van Zoelen
A. E. G. Lenferink
M. J. H. van Vugt
M. L. M. van de Poll
Introduction
83(1)
Chimeric growth factors
84(1)
EGF-related factors and their receptors
85(5)
EGF-related factors
85(1)
Receptors for the EGF-related factors
86(1)
Structure-function relationship of EGF and TGFα
87(2)
Chimeric proteins of the EGF family
89(1)
Preparation and isolation of recombinant EGF-like growth factors
90(8)
Introduction
90(3)
Construction and expression of EGF/TGFα chimeras
93(5)
Characterization of EGF/TGFα domain-exchange mutants
98(11)
Introduction
98(7)
Functional studies on EGF/TGFα chimeras
105(1)
Acknowledgements
105(1)
References
105(4)
Structure-activity relationships of chemokines
109(16)
Ian Clark-Lewis
Jennifer Anderson
Philip Owen
Luan Vo
Jiang-Hong Gong
Introduction
109(3)
Chemokines
110(1)
Primary structure: practical considerations
110(1)
Importance of the 3D structure
111(1)
Design: testing an hypothesis
112(1)
Single substitutions
112(1)
Multiple substitutions
112(1)
Hybrids/chimeras
112(1)
Purification, folding, and analysis
113(6)
Sample preparation and RP-HPLC analysis
113(2)
Folding
115(1)
Purification
116(2)
Verification of covalent structure
118(1)
Handling and storage
118(1)
Functional assays
119(1)
General considerations
119(1)
Cell migration
119(1)
Receptor binding
120(5)
Iodination of chemokines
120(2)
Receptor binding assays
122(1)
Bindability and kinetics
123(1)
References
123(2)
Generation and selection of RNA ligands that inhibit the interaction of vascular permeability factor/vascular endothelial growth factor (VPF/VEGF) with its receptors
125(24)
Louis S. Green
Nebojsa Janjic
Introduction to the SELEX process
125(1)
Application of the SELEX process to identifying RNA ligands to VPF/VEGF
126(11)
Random RNA libraries
126(3)
Selection conditions
129(2)
Consensus sequence and secondary structure identification
131(2)
Minimal sequence determination
133(1)
Selection of VPF/VEGF anatgonists: inhibition of receptor binding
134(3)
Methods for making RNA ligands nuclease resistant
137(6)
Clinical applications of VPF/VEGF antagonists
143(6)
References
146(3)
Immunolocalization and RT-PCR for the detection and quantification of growth factor and receptor gene expression
149(26)
Simon R. Myers
Harshad A. Navsaria
Introduction
149(2)
Assays of protein expression in tissues
149(1)
Assays of mRNA expression in tissues
150(1)
Immunolocalization of growth factor and receptor protein
151(6)
Introduction
151(1)
Tissue preparation
151(1)
Storage and dilution of antibodies
152(1)
Detection methods
152(1)
Controls
153(2)
Immunohistochemistry
155(2)
Semi-quantification of immunohistochemistry by computer image analysis
157(2)
Introduction
157(1)
Average OD measurement
158(1)
Interpretation of immunohistochemistry results
159(2)
Semi-quantification of mRNA levels using non-competitive RT-PCR
161(7)
Introduction
161(1)
Extraction of total RNA from small tissue specimens
162(1)
Reverse transcription of mRNA to cDNA
163(1)
PCR amplification of mRNA-derived cDNA with specific oligonucleotide primers
164(2)
Detection of RT-PCR product and quantification
166(2)
Competitive RT-PCR quantification of specific mRNA levels
168(3)
Introduction
168(1)
Mutant templates
168(2)
Use of mutant templates in tissue analysis
170(1)
Interpretation of RT-PCR amplification analyses of gene expression
171(4)
References
173(2)
Defining growth factor function through tissue-specific expression of dominant-negative receptor mutants
175(24)
Sabine Werner
Introduction
175(3)
The concept of dominant-negative growth factor receptors
176(1)
Examples of efficient use of dominant-negative growth factor receptors in transgenic mice
177(1)
Design and synthesis of a gene encoding a dominant-negative receptor mutant
178(1)
Identification of transgenic mice
179(2)
Analysis of transgene expression
181(7)
Advantages and disadvantages of various RNA detection methods
181(1)
RNase protection assay
182(6)
In situ detection of transgene mRNA and protein
188(1)
Characterization of the skin of transgenic mice
188(11)
Histological analysis
188(2)
Analysis of differentiation-specific proteins in the epidermis
190(3)
Labelling of proliferating cells with 5-bromo-2'-deoxyuridine (BrdU)
193(2)
Acknowledgements
195(1)
References
196(3)
Growth factor-toxin chimeras and their applications
199(28)
Pamela A. Davol
A. Raymond Frackelton, Jr.
Paul Calabresi
Introduction
199(1)
Detecting chimeric function
200(14)
Evaluating cytotoxicity as a function of toxin activity
200(3)
Evaluating cytotoxicity as a function of receptor specificity
203(5)
Quantitating cytotoxic activity on various cell lines
208(2)
Assessing antitumour effects in animals
210(4)
Clinical applications of growth factor-toxin chimeras
214(2)
Cancer therapy
214(1)
Other applications
215(1)
Potential problems in using biologically active chimeras
216(7)
Pitfalls associated with the toxin moiety
217(1)
Adverse effects associated with growth factor-toxin chimeras
217(2)
Mechanisms of resistance
219(4)
Conclusions
223(4)
References
223(4)
Gene therapy applications of growth factors
227(38)
Tor Svensjo
Feng Yao
Bohdan Pomahac
Elof Eriksson
Introduction to gene therapy applications of growth factors
227(7)
Gene transfer methods
228(4)
Gene therapy with growth factors
232(2)
Growth factor applications to enhance cutaneous wound healing
234(1)
Growth factor expression in skin
235(8)
Detecting growth factor expression in target organs
243(4)
Determining the effects of growth factors on wound healing
247(1)
Summary
248(5)
References
248(5)
Appendices
A1 Growth factors
253(6)
A2 Amino acid abbreviations
259(2)
A3 Names and addresses of suppliers
261(4)
Index 265

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