Combinatorial libraries : synthesis, screening, and application potential /
Clasificación: | Libro Electrónico |
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Otros Autores: | |
Formato: | Electrónico eBook |
Idioma: | Inglés |
Publicado: |
New York :
Walter de Gruyter,
1996.
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Temas: | |
Acceso en línea: | Texto completo |
Tabla de Contenidos:
- Contents
- A Synthetic Peptide Libraries
- 1 Soluble Synthetic Combinatorial Libraries: The Use of Molecular Diversities for Drug Discovery
- 1.1 Introduction
- 1.2 Synthetic Combinatorial Libraries (SCLs)
- 1.3 Synthetic Methods for the Generation of SCLs
- 1.4 SCLs in Drug Discovery and Basic Research
- 1.5 Conclusion
- 2 Combinatorial Libraries of Synthetic Structures: Synthesis, Screening, and Structure Determination
- 2.1 Introduction
- 2.2 One-Bead One-Structure Concept
- 2.3 Design and Synthesis of Non-Peptide Libraries
- 2.4 Release Assay
- 2.5 Stucture Determination2.6 Conclusion
- 3 Peptide Libraries Bound to Continuous Cellulose Membranes: Tools to study Molecular Recognition
- 3.1 Introduction
- 3.2 Detection of antibody epitopes
- 3.3 Mutational analyses of peptide epitopes
- 3.4 Positional scanning combinatorial library
- 3.5 Indentification of metal binding peptides
- 3.6 Summary
- B Nucleic Acids Libraries
- 4 In Vitro Selection of Nucleic Acid Sequences that Bind Small Molecules
- 4.1 Introduction
- 4.2 Natural RNA Receptors
- 4.3 In Vitro Selection
- 4.4 Amino Acid Aptamers4.5 Cofactors
- 4.6 DNA Aptamers
- 4.7 The Complexity of Complexity
- 4.8 Aptamer Structures
- 4.9 Transition State Stabilization and Tight Binding
- 4.10 Conclusions
- 5 Discovery and Characterization of a Thrombin Aptamer Selected from a Combinatorial ssDNA Library
- 5.1 Introduction
- 5.2 Discovery and Initial Characterization
- 5.3 Structure
- 5.4 Binding Site on Thrombin
- 5.5 Determination of Kd and Ki
- 5.6 In vitro Activity
- 5.7 In Vitro Activity
- 5.8 Conclusions
- C Phage Display of Peptide Libraries
- 6 Structural and Functional Constraints in the Display of Peptides on Filamentous Phage Capsids6.1 Introduction
- 6.2 The Phage Life Cycle
- 6.3 A Low Resolution Model
- 6.4 Extending the Amino-Terminus of pVIII
- 6.5 Modifying the Surface of Filamentous Phage by Amino Acid Substitution
- 6.6 Can the Remaining Minor Proteins Support Modification?
- 7 Conformationally Defined Peptide Libraries on Phage: Selectable Templates for the Design of Pharmacological Agents
- 7.1 Introduction
- 7.2 From Peptides to Peptidomimetics
- 7.3 Building Constraints in Phage-Displayed Polypeptides7.4 The Minibody: An Engineered ß-Pleated Scaffold for the Display of Reverse-Turn Motifs
- 7.5 The Zinc Finger: A Small Domain for the Display of Structurally Homogeneous α-Helical Motifs
- 7.6 Future Developments: Progressing Toward Non-Peptide Pharmaceuticals
- 8 Discovery of Disease-Specific Mimotopes by Screening Phage Libraries with Human Serum Samples
- 8.1 Introduction
- 8.2 Using Polyclonal Antibodies as a Ligate for the Selection of RPL