MHC Molecules: Expression, Assembly and Function

3 nant expression systems have been used to make MHC molecules con­ taining a single peptide of interest. To date, fifteen single peptide class I structures (incorporating three different HLA and two different H-2 allotypes/isotypes) and four additional class II structures (two single peptide comple...

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Bibliographic Details
Main Authors: Urban, Robert G., Chicz, Roman M. (Author)
Format: eBook
Language:English
Published: New York, NY Springer US 1996, 1996
Edition:1st ed. 1996
Subjects:
Online Access:
Collection: Springer Book Archives -2004 - Collection details see MPG.ReNa
Table of Contents:
  • Relating Specificity to the Structure of Polymorphic TAP Molecules
  • Length of Transported Peptides
  • TAP-Dependent and Independent Presentation
  • TAP and Disease
  • Concluding Remarks
  • 4. Molecular Chaperones in MHC Class I and Class II Biosynthesis and Assembly
  • Introduction: ER Resident Molecular Chaperones
  • Molecular Chaperones Implicated in Class I Biosynthesis and Assembly
  • Molecular Chaperones Implicated in MHC Class II Biosynthesis and Assembly
  • Quality Control of MHC Molecules Mediated by Molecular Chaperones
  • 5. Polypeptide Release from Lysosomes
  • Synthesis and Transport of Lysosomal Hydrolases
  • Entry of Degradation Substrates
  • Lysosomal Hydrolysis
  • Polypeptide Release from Lysosomes
  • Possible Immunological Relevance
  • Conclusion
  • 6. Intracellular Trafficking of MHC Class II Molecules
  • Assembly of MHC Class II Molecules in the ER and Early Stages of Transport
  • Processing Intermediates of Invariant Chain
  • 16. Peptide-Mediated Regulation of Allergic Diseases
  • The Role of CD4+ T Cell Subsets
  • The Immunological Objectives of Allergy Therapy
  • Regulation of Specific T Cells by Peptides
  • Deviation of Thl/Th2 Phenotype of the Responder Population
  • 17. Genetic Modulation of Antigen Presentation
  • Vaccines
  • Genetic Immunization for Viral Diseases
  • Treatment of Autoimmune Disease
  • Conclusion
  • Post-Golgi Trafficking of MHC Class II Molecules and Sites of Invariant Chain Degradation
  • Intracellular Sites of Assembly of Peptide:MHC Class II Complexes
  • 7. The Role of HLA-DM in Class II Antigen Presentation
  • DM Sequence and Structure
  • Regulation of Expression
  • Genomic Organization of DM Genes
  • Evolutionary Considerations
  • DM Polymorphism
  • Analysis of DM Mutant Cells
  • The Mechanism of DM Action
  • The Biology of Antigen Processing
  • The Biosynthesis and Maturation of Class II
  • Conclusion
  • 8. Crystallographic Analysis of Peptide Binding by Class I and Class II Major Histocompatibility Antigens
  • Class I Major Histocompatibility Antigens
  • Class II Major Histocompatibility Antigens
  • Similarities and Differences Between Class I and Class II Major Histocompatibility Antigens
  • 9. HLA and Disease: Molecular Basis
  • Tissue Typing Techniques
  • Epidemiological Analysis
  • Paradigms of Diseases Associated with the MHC
  • HLA-B27 and Ankylosing Spondylitis
  • Concluding Remarks
  • 13. Cooperative Recognition of MHC Class II Molecules:Peptide Complexes by the T Cell Receptor and CD4
  • TCR Recognition of MHC Class II:Peptide Complexes
  • CD4 Binding to MHC Class II Molecules
  • CD4 Interaction With the TCR:CD3 Complex
  • Conclusions
  • 14. Receptors for MHC Class I Molecules in Human Natural Killer Cells
  • MHC Class I Molecules Inhibit NK Cell Cytotoxicity
  • Murine NK Inhibitory Receptors
  • Human NK Inhibitory Receptors
  • A New Family of Immunoglobulin-Superfamily (Ig-SF) Genes Selectively Expressed in Human NK Cells
  • Evidence That NK-Specific Ig-SF Genes May Encode Human Receptors for Class I Molecules
  • NK Recognition of MHC Class I Molecules Is Mediated by a Complex System
  • 15. The MHC in Host-Pathogen Evolution
  • Selection Acting on the Human Host
  • Pathogen Avoidance of T Cell Recognition
  • Mechanisms of Decreasing Antigen Presentation
  • Mechanisms of Avoiding T Cell Recognition of Specific Epitopes
  • Perspective
  • 1. Major Histocompatibility Antigens: An Introduction
  • 2. The Major Histocompatibility Complex Genes and Their Transcriptional Regulation
  • The Murine Major Histocompatibility Complex
  • The Major Histocompatibility Complex of Humans, the HLA
  • Developmental and Tissue-Specific Expression of MHC Genes
  • Role of Aberrant Expression of MHC Gene Products in Immunologic Disease
  • Cis-Elements and Transcription Factors That Control MHC Class I Gene Expression
  • Factors and Elements That Control MHC Class II Gene Expression
  • Models of Activation and Repression
  • Concluding Comments
  • 3. TAP Peptide Transporters and Antigen Presentation
  • Evidence for Peptide Translocation by TAP
  • Tap Genes and Sequences
  • TAP as Member of the ABC Transporter Family
  • Structure and Assembly of the TAP Complex
  • In Vitro Assays for Peptide Binding and Transport by TAP
  • Sequence Specificity of Peptide Transport by Different TAP Molecules
  • MHC II and Disease
  • Concluding Remarks
  • 10. Epitope Prediction Algorithms for Class I MHC Molecules
  • Elucidation of Peptide-Binding Motifs
  • Anchor Residues
  • Peptide-Binding Assays
  • Physical Basis for Peptide-Binding Motifs
  • Prediction of Binding Peptides
  • Exceptional Peptides
  • Peptide Binding and Antigenicity
  • Conclusions
  • 11. Options for TCR Interactions: TCR Agonists, Antagonists and Partial Agonists
  • Introduction: Smart and Dumb T Cell Receptors
  • Full Agonists, Partial Agonists and Antagonists
  • What Do TCR Partial Agonists and Antagonists Do?
  • T Cell Development
  • The Direction of Mature T Cell Responses
  • The Two Edged Sword: Antagonists as Protectors and Perpetrators of Disease
  • How Do Antagonist/Partial Agonists Work?
  • Concluding Remarks
  • 12. Role of Ligand Density in T Cell Reactions
  • Background
  • The Study of Peptides Recognized by CD8+ CTL
  • What Determines the Efficacy of CTL-Mediated Target Cell Lysis?
  • Role of Ligand Density