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  • 1
    Online Resource
    Online Resource
    Cham :Springer International Publishing AG,
    Keywords: Proteomics. ; Electronic books.
    Type of Medium: Online Resource
    Pages: 1 online resource (420 pages)
    Edition: 1st ed.
    ISBN: 9783030111434
    Series Statement: Current Topics in Microbiology and Immunology Series ; v.420
    DDC: 572.6
    Language: English
    Note: Intro -- Preface -- Contents -- 128 Activity-Based Protein Profiling-Enabling Multimodal Functional Studies of Microbial Communities -- Abstract -- 1 Introduction -- 2 Probe Design -- 2.1 Activity- and Affinity-Based Probes for Multimodal Characterization of Microbiome Function -- 2.2 Click Chemistry and Sample Analysis -- 3 Challenges of Microbiome Proteomics and How ABPP Can Facilitate -- 4 Biological Applications for ABPP -- 4.1 Host-Associated Microbial Communities -- 4.1.1 Xenobiotic Metabolism -- 4.1.2 Bile Acid Metabolism and Signaling -- 4.2 Environmental Microbial Communities -- 4.2.1 Metabolic Activity and Translation -- 4.2.2 Vitamin Metabolism -- 4.2.3 Community Signaling -- 5 Current Challenges and Outlook -- References -- 135 Activity-Based Protein Profiling Methods to Study Bacteria: The Power of Small-Molecule Electrophiles -- Abstract -- 1 Introduction -- 1.1 Activity-Based Probes: What They Are and How They Work -- 2 Probe Design Strategies -- 2.1 Reactive Warhead and Recognition Elements -- 2.2 Linker -- 2.3 Reporter -- 2.3.1 Quenched Activity-Based Probes -- 2.3.2 Bioorthogonal Ligation Reactions -- 3 Detection Methods -- 3.1 Gel-Based Detection -- 3.2 Live-Cell Imaging -- 3.3 Mass Spectrometry -- 4 ABPP in Bacteria -- 4.1 Serine-Reactive Probes -- 4.2 Cysteine-Reactive Probes -- 4.3 Antibiotic-Derived Probes -- 4.4 Carbohydrate-Based Probes -- 4.5 Probes Inspired by Natural Products -- 5 Application of ABPP in Natural Product Target Discovery -- 6 Conclusion -- References -- 125 Opportunities and Challenges in Activity-Based Protein Profiling of Mycobacteria -- Abstract -- 1 Introduction -- 2 Activity-Based Protein Profiling in Mycobacterium tuberculosis -- 2.1 Profiling of ATP-Binding Proteins -- 2.2 Profiling of Serine Hydrolase Enzymes -- 3 Development of Activity-Based Probes for Applications to Mycobacteria. , 3.1 Activity-Based Probe for the Adenylating Enzyme MbtA -- 3.2 Activity-Based Probe for the Serine Protease Hip1 -- 4 Identification of Inhibitor Targets Using ABPP in Mycobacteria -- 4.1 Targets of Tetrahydrolipstatin -- 4.2 Targets of the β-Lactone EZ210 -- 4.3 Targets of Staurosporine -- 4.4 Using Activity-Based Protein Profiling to Investigate Inhibitor Mechanism of Action -- 5 Summary and Outlook -- Acknowledgements -- References -- 129 Activity-Based Protein Profiling at the Host-Pathogen Interface -- Abstract -- 1 Introduction -- 2 Applications of ABPP to In Vitro Models of Microbial Infection -- 2.1 Detecting Host Enzymes Active in Infected Cells -- 2.2 Profiling Pathogen Adaptation to the Host Environment -- 3 Applications of ABPP to Infected Plants -- 3.1 Discovery of Pathogen-Secreted Protease Inhibitors -- 3.2 Global Profiling of Active Enzymes -- 3.3 Mechanistic Studies of Proteasome Activity and Inhibition -- 4 Applications of ABPP to Infected Animals -- 5 Applications of ABPP to Inhibitor Discovery and Characterization -- 5.1 Identifying the Targets of Bioactive Inhibitors -- 5.2 High-Throughput Screens for Selective Inhibitors -- 5.3 Rational Design and Optimization of Inhibitors -- 6 Concluding Remarks -- Acknowledgements -- References -- 126 Chemical Proteomic Profiling of Protein Fatty-Acylation in Microbial Pathogens -- Abstract -- 1 Introduction -- 2 Protein Fatty-Acylation -- 2.1 N-myristoylation -- 2.2 S-palmitoylation -- 2.3 Nε-Lys-Fatty-Acylation -- 3 Chemical Proteomic Methods for Profiling Fatty-Acylation -- 3.1 Chemical Reporter Strategy for Studying Fatty-Acylation -- 3.2 Acyl-Biotin Exchange (ABE) Strategy for Studying S-palmitoylation -- 4 Proteomic Profiling of Fatty-Acylation in Eukaryotic Pathogens -- 4.1 Proteomic Profiling of N-myristoylation in Parasites -- 4.2 Proteomic Profiling of S-palmitoylation in Parasites. , 4.3 Proteomic Profiling of N-myristoylation and S-palmitoylation in Fungal Pathogens -- 5 Protein Fatty-Acylation in Bacterial Virulence -- 5.1 Host-Mediated Fatty-Acylation of Bacterial Effectors -- 5.2 Modulation of Host Fatty-Acylation by Bacterial Effectors -- 6 Conclusions -- References -- 134 How to Target Viral and Bacterial Effector Proteins Interfering with Ubiquitin Signaling -- Abstract -- 1 Introduction -- 2 The Current Toolbox -- 2.1 DUB Targeting Covalent Probes -- 2.2 E1-E2-E3 Targeting Covalent Probes -- 2.3 Assay Reagents -- 2.4 (Poly)Ub Chains -- 3 Applications -- 3.1 Applications in Virology -- 3.2 Applications in Bacteriology -- 3.3 Legionella Effector Enzymes: The Odd-Ones Out -- 4 Conclusions -- References -- 139 ABPP and Host-Virus Interactions -- Abstract -- 1 Introduction -- 2 Viral Entry -- 3 Viral Replication -- 3.1 Role of Triglycerides -- 3.2 Role of Phosphatidylinositides -- 3.3 Role of Cholesterol -- 4 Programmed Cell Death -- 5 Viral Evasion of the Immune Response -- 5.1 Viral Alterations to Proteasome Activity -- 5.2 NFκB Signalling During Herpesvirus Infection -- 5.3 Virally Encoded Deubiquitinases -- 6 Viral Assembly and Egress -- 7 Selective Labelling of Individual Viral Enzymes -- 8 Future Objectives -- 9 Conclusions -- References -- 123 Activity-Based Protein Profiling for the Study of Parasite Biology -- Abstract -- 1 Background -- 2 Activity-Based Probes for Target Discovery in Parasites -- 2.1 Profiling Protease Activity -- 2.1.1 Cysteine Proteases -- 2.1.2 Serine Proteases -- 2.1.3 Threonine Proteases -- 2.1.4 Aspartyl and Metalloproteases -- 2.2 Profiling Acyl-Protein Thioesterases -- 2.3 Profiling Protein Kinases -- 3 Activity-Based Protein Profiling in Parasites: An Exciting Future -- References -- 124 Deciphering T Cell Immunometabolism with Activity-Based Protein Profiling -- Abstract -- 1 Introduction. , 1.1 Cellular Interactions that Regulate T Cell Responses -- 1.2 Cell Signaling in T Cell Responses -- 1.3 Cell Metabolism in T Cell Responses -- 1.4 Fate Decisions in T Cells -- 2 Features of Dysfunctional T Cells -- 2.1 Anergy/Tolerance -- 2.2 Dysfunction/Exhaustion -- 2.3 Extrinsic Regulation of T Cell Metabolism -- 2.4 New Opportunities for ABPP Discovery in T Cell Biology -- 3 Functional Insights into T Cell Biology Using ABPP Methods -- 3.1 ABPP Technology -- 3.2 ABPP Discovery of Dimethyl Fumarate Mode of Action in T Cells -- 3.3 ABPP Discovery of New Metabolic Regulators of T Cell Proliferation -- 3.4 ABPP Discovery of Proteasome Regulation of T Cell Fate -- 4 Using ABPP to Probe Immunometabolism in the Tumor Microenvironment -- 4.1 Diacylglycerol Signaling as an Intrinsic Regulator of TCR Activation -- 4.1.1 Diacylglycerol Kinase Family and Biochemistry -- 4.1.2 ABPP Discovery of Novel Druggable Sites of DGKs -- 4.1.3 ABPP Strategies for Discovery of DGK Inhibitors -- 4.2 Extrinsic Regulators of T Cell Metabolism -- 4.2.1 Metabolic Checkpoints in Glycolysis -- 4.2.2 Glutamine Dependence for Effector Function -- 4.2.3 Immunosuppression by Tryptophan Depletion -- 5 Conclusions -- References -- 137 Small-Molecule Inhibitors of PARPs: From Tools for Investigating ADP-Ribosylation to Therapeutics -- Abstract -- 1 Introduction -- 1.1 The PARP Family -- 1.2 Summary of Review -- 2 Common and Distinct Features in the Catalytic Domain of PARPs -- 2.1 The NAD+ Binding Domain -- 2.2 HYE Versus HYΦ PARPs -- 2.3 Non-Conserved Loops -- 3 Early Developments in the Field: Initial Focus on Small-Molecule Inhibitors of PARP1 -- 3.1 The Founding PARP Inhibitors -- 3.2 PARP1/2 Identified as Therapeutic Targets in Cancer -- 4 Moving Beyond PARP1/2 -- 4.1 Forward Chemical Genetic Screen Identifies a Small-Molecule Inhibitor of PARP5a/b. , 4.2 A Dearth of Selective and Potent Inhibitors for the HYΦ PARP Subfamily -- 5 Structural Studies of PARP Inhibitors: Insights into Inhibitor Potency and Selectivity -- 5.1 Structural Studies of HYE PARP Inhibitors -- 5.2 Structural Studies of HYΦ PARP Inhibitors -- 5.3 Pharmacophore for PARP Inhibitors -- 6 Chemical and Biological Reagents for Measuring PARP Activity -- 6.1 NAD+ Analogs for In Vitro Analysis -- 6.2 Detection Methods with Endogenous NAD+ -- 7 Assessing PARP Inhibitor Selectivity Across the PARP Family -- 7.1 Profiling Using Protein Stabilization Reveals Lack of Selectivity of Many PARP Inhibitors -- 7.2 Polypharmacology Among PARP Inhibitors -- 8 Conclusions and Future Directions -- References -- 132 Development of Activity-Based Proteomic Probes for Protein Citrullination -- Abstract -- 1 Introduction -- 2 PAD Structure and Function -- 2.1 PAD Structures -- 2.2 PAD Substrate Recognition and Catalytic Mechanism -- 3 PAD Inhibitors -- 3.1 Reversible PAD Inhibitors -- 3.2 Irreversible PAD Inhibitors -- 4 Activity-Based Proteomic Probes Targeting the PADs -- 4.1 First-Generation PAD-Targeted ABPPs -- 4.2 Second-Generation PAD-Targeted ABPPs -- 4.3 Phenylglyoxal-Based Probes to Detect Protein Citrullination -- 5 Conclusions -- References -- 138 Recent Advances in Activity-Based Protein Profiling of Proteases -- Abstract -- 1 Introduction -- 2 Influencing Selectivity -- 2.1 Non-natural Amino Acids -- 2.2 Application of Antibodies -- 2.3 Modification of Target Proteases -- 3 Detection Tags -- 3.1 Fluorophores -- 3.2 Isotopes -- 3.2.1 Stable Isotopes -- 3.2.2 Radioactive Isotopes -- 3.3 Biotin and Detection by MS -- 3.4 Dual Detection -- 4 Examples of ABPP on Specific Proteases -- 4.1 Neutrophil Serine Proteases -- 4.2 Caspases -- 4.3 Malt1 -- 4.4 The Proteasome -- 4.5 Matriptase -- 5 Conclusions & -- Future Directions. , Acknowledgements.
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  • 2
    Online Resource
    Online Resource
    Milton :Taylor & Francis Group,
    Keywords: Proteins -- Textbooks. ; Electronic books.
    Description / Table of Contents: Authored by key players in the field, this volume offers a relevant presentation of peptide and protein chemistry. It provides key insight into the fast-developing field of proteomics, including structural and functional aspects, biochip development, and clinical potential. It includes chapters on bioinformatics and proteomics and presents the latest information on concerns over protein degradation and the post-translational modifications of proteins and peptides. The book also includes a section on protein-coupled diseases that presents increasing evidence of the pathological impact of protein misfolding in relation to various neurodegenerative diseases, as well as a section on the role of proteins in cancer.
    Type of Medium: Online Resource
    Pages: 1 online resource (440 pages)
    Edition: 1st ed.
    ISBN: 9781439882047
    DDC: 572.65
    Language: English
    Note: Front cover -- Contents -- Preface -- Further Reading -- Biography -- From Building Blocks to 3-D Structure -- Introduction to Part I -- Chapter 1. Amino Acids -- Chapter 2. Noncovalent Interactions -- Chapter 3. Structural Organization of Proteins -- Protein Biosynthesis and Posttranslational Modifications -- Chapter 4. The Biosynthesis of Proteins -- Chapter 5. Posttranslational Modifications -- Folding of Proteins -- Chapter 6. Protein Folding -- Chapter 7. Intracellular Sorting of Proteins -- Protein Degradation -- Chapter 8. Protein Turnover -- Introduction to Part II -- Chaper 9. Purification and Characterization of Proteins -- Chapter 10. Crystallography and X-Ray Diffraction -- Chapter 11. Optical Spectroscopy -- Chapter 12. Nuclear Magnetic Resonance (NMR) -- Chapter 13. Methods to Follow Protein Folding -- Chapter 14. Mass Spectrometry -- Chapter 15. Chemical Synthesis of Peptides and Proteins -- Introduction to Part III -- Chapter 16. Protein Engineering and Gene Silencing -- Chapter 17. Protein-Ligand Interactions -- Chapter 18. Sequence Analysis and Function Prediction -- Chapter 19. Protein Structure Prediction -- Chapter 20. Proteomics -- Introduction to Part IV -- Chapter 21. Enzymes -- Chapter 22. Nucleic Acid- Binding Proteins -- Chapter 23. Cell Surface Receptors and Signaling -- Chapter 24. Membrane Proteins -- Chapter 25. Antibodies -- Chapter 26. Fibrous Proteins -- Chapter 27. Selected Classes of Bioactive Peptides -- Introduction to Part V -- Chapter 28. Misfolding-Based Diseases -- Chapter 29. Miscleavage-Based Diseases -- Chapter 30. Missequence-Based Diseases -- Chapter 31. Peptides and Proteins as Drugs -- Index -- Back cover.
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  • 3
    Online Resource
    Online Resource
    Cham : Springer International Publishing
    Keywords: Microbiology ; Medical virology ; Microbiology ; Medical virology ; Immunology ; Immunology ; Medical microbiology. ; Virology. ; Protein Array Analysis ; Protein Interaction Mapping ; Host-Pathogen Interactions ; Proteomics methods
    Description / Table of Contents: This volume provides a collection of contemporary perspectives on using activity-based protein profiling (ABPP) for biological discoveries in protein science, microbiology, and immunology. A common theme throughout is the special utility of ABPP to interrogate protein function and small-molecule interactions on a global scale in native biological systems. Each chapter showcases distinct advantages of ABPP applied to diverse protein classes and biological systems. As such, the book offers readers valuable insights into the basic principles of ABPP technology and how to apply this approach to biological questions ranging from the study of post-translational modifications to targeting bacterial effectors in host-pathogen interactions
    Type of Medium: Online Resource
    Pages: Online-Ressource (X, 417 p. 115 illus., 70 illus. in color, online resource)
    Edition: Springer eBook Collection. Biomedical and Life Sciences
    ISBN: 9783030111434
    Series Statement: Current Topics in Microbiology and Immunology 420
    Language: English
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  • 4
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Journal of the American Chemical Society 116 (1994), S. 6013-6014 
    ISSN: 1520-5126
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Oxford UK : Blackwell Science Ltd.
    Journal of neurochemistry 72 (1999), S. 0 
    ISSN: 1471-4159
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: Abstract: Oleamide is an endogenous lipid that accumulates duringsleep deprivation and has hypothermic effects when administered to rodents.The mechanisms for its activity remain unknown. Intraperitoneal injections ofoleamide elicited dramatic increases in content of c-fos mRNA and Fosprotein in distinct brain regions, including cingulate and somatosensorycortical areas and numerous nuclei of the thalamus and hypothalamus,indicating that there are explicit targets for its action. In the thalamus andhypothalamus a majority of neurons induced for c-fos expression alsoexpressed the serotonin 5-HT7 receptor, an allosteric target foroleamide in in vitro studies. These data suggest that oleamide may act at5-HT7 receptors to elicit alterations in transcription that result in some of its physiological effects.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of organic chemistry 59 (1994), S. 5078-5079 
    ISSN: 1520-6904
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature biotechnology 23 (2005), S. 1303-1307 
    ISSN: 1546-1696
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: [Auszug] Chemical genomics aims to discover small molecules that affect biological processes through the perturbation of protein function. However, determining the protein targets of bioactive compounds remains a formidable challenge. We address this problem here through the creation of a natural ...
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature biotechnology 21 (2003), S. 687-691 
    ISSN: 1546-1696
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: [Auszug] To realize the promise of genomics-based therapeutics, new methods are needed to accelerate the discovery of small molecules that selectively modulate protein activity. Toward this end, advances in combinatorial synthesis have provided unprecedented access to large compound libraries ...
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature biotechnology 20 (2002), S. 805-809 
    ISSN: 1546-1696
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: [Auszug] Proteomics research requires methods to characterize the expression and function of proteins in complex mixtures. Toward this end, chemical probes that incorporate known affinity labeling agents have facilitated the activity-based profiling of certain enzyme families. To accelerate ...
    Type of Medium: Electronic Resource
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  • 10
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] Rat liver plasma membranes were isolated as described5 and solubilized in 10% glycerol, 1 mM EDTA, 20 mM HEPES, pH 7.2 (solubilization buffer) with 1% Triton X-100. From the detergent-solubilized fraction of the liver plasma membranes, oleamide hydrolase activity was partially purified by using a ...
    Type of Medium: Electronic Resource
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