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ویرایش: 1st ed. 2023
نویسندگان: Mohamed A. Elsawy (editor)
سری:
ISBN (شابک) : 3031293592, 9783031293597
ناشر: Springer
سال نشر: 2023
تعداد صفحات: 556
زبان: English
فرمت فایل : PDF (درصورت درخواست کاربر به PDF، EPUB یا AZW3 تبدیل می شود)
حجم فایل: 20 مگابایت
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در صورت تبدیل فایل کتاب Peptide Bionanomaterials: From Design to Application به فرمت های PDF، EPUB، AZW3، MOBI و یا DJVU می توانید به پشتیبان اطلاع دهید تا فایل مورد نظر را تبدیل نمایند.
توجه داشته باشید کتاب بیونانومادهای پپتیدی: از طراحی تا کاربرد نسخه زبان اصلی می باشد و کتاب ترجمه شده به فارسی نمی باشد. وبسایت اینترنشنال لایبرری ارائه دهنده کتاب های زبان اصلی می باشد و هیچ گونه کتاب ترجمه شده یا نوشته شده به فارسی را ارائه نمی دهد.
Preface Contents Chapter 1: Design Rules for Self-Assembling Peptide Nanostructures 1.1 Nature: Source of Inspiration 1.2 Amino Acids: The Building Units 1.3 Molecular Design of Self-Assembling Peptides: The Building Blocks 1.3.1 Biosynthetic Polypeptides 1.3.1.1 Collagen-Like Polypeptides 1.3.1.2 Elastin-Like Polypeptides 1.3.1.3 Silk-Elastin-Like Polypeptides 1.3.1.4 Keratin and Keratin-Like Polypeptides 1.3.1.5 Resilin-Like Polypeptides 1.3.2 De Novo Synthetic Short Peptides 1.3.2.1 β-Sheet Forming Peptides 1.3.2.2 β-Hairpin-Forming Peptides 1.3.2.3 α-Helix/Coiled-Coil-Forming Peptides 1.3.2.4 Amphiphilic Peptides Amphiphilic Peptide Sequences Lipidated Peptides 1.3.2.5 Short Aromatic Peptides 1.3.2.6 Cyclic Peptides 1.4 Summary References Chapter 2: β-Sheet and β-Hairpin Peptide Nanomaterials 2.1 Introduction 2.2 Early Investigations of β-Sheet Peptide Assemblies as Materials 2.3 Short Amphipathic β-Sheet Peptides 2.3.1 Ionic Self-Complementary Peptides: EAK16 and RAD16 2.3.2 (FKFE)n and Related Amphipathic Peptide Sequences from the EAK/RAD Family 2.3.3 P11 Peptides and Related Sequences 2.3.4 Multidomain Peptides 2.4 β-Hairpin Self-Assembling Peptides 2.5 Surfactant-Like Peptide Assemblies 2.6 Conclusion References Chapter 3: α-Helix and Coiled-Coil Peptide Nanomaterials 3.1 Scope of This Chapter 3.2 De Novo Design of α-Helical Coiled Coils 3.3 α-Helical Peptide Fibers 3.4 α-Helical Peptide Nanotubes 3.5 α-Helical Peptide Cages and Protein Origami 3.6 α-Helical Peptide Networks and Arrays 3.7 Conclusions References Chapter 4: Ultra-Short Peptide Nanomaterials 4.1 Introduction 4.1.1 Definition of Ultra-Short Peptide 4.1.2 A Brief History of Short and Ultra-Short Peptide Nanomaterials 4.1.3 General Mechanism of Self-Aggregation 4.2 Nanotubes 4.3 Hydrogels 4.4 Adhesives 4.5 Conclusions and Future Perspectives References Chapter 5: Peptide Amphiphile Nanomaterials 5.1 Introduction 5.2 Classification 5.2.1 Amphiphilic Peptides 5.2.1.1 PAs with Alternate Hydrophilic-Hydrophobic Amino Acid Sequence 5.2.1.2 PAs with Hydrophilic Sequence Connected with Hydrophobic Stretch 5.2.1.3 Block co-Polypeptide Amphiphiles 5.2.2 Lipidated Peptide Amphiphiles 5.2.3 Cyclic Peptide Amphiphiles 5.2.4 Supramolecular Peptide Amphiphiles 5.3 Self-Assembly and Nanostructures 5.3.1 Interactions Accountable for PA Self-Assembly 5.3.1.1 Hydrogen Bonding 5.3.1.2 Hydrophobic Interaction 5.3.1.3 Electrostatic Interactions 5.3.1.4 π-π Stacking 5.3.1.5 Van der Waals Interactions 5.3.1.6 Other Unusual Interactions 5.3.2 Nanoassemblies of PAs 5.3.3 Thermodynamic and Kinetics of PA Self-Assemblies 5.3.4 Stimuli-Responsive Assemblies of PAs 5.3.4.1 pH Responsive 5.3.4.2 Redox Responsive 5.3.4.3 Biocatalyst Responsive 5.4 Application-Specific Design and Execution Guideline 5.5 Applications of PA Assemblies 5.5.1 Tissue Engineering 5.5.2 As Delivery Vehicles 5.5.3 Wound Healing 5.5.4 Antimicrobial PAs 5.5.5 Mineralization and Nanofabrication 5.5.6 Conductive Materials 5.5.7 Biomimics and Systems Chemistry 5.6 Concluding Remarks References Chapter 6: Polypeptide-Based Multicomponent Materials: From Design to Applications 6.1 Introduction 6.2 Design Strategies for Engineered Polypeptides 6.2.1 Incorporating Unnatural Amino Acids 6.2.2 Posttranslational Modifications of Polypeptides 6.2.3 Incorporation of Cross-Linking Moieties 6.3 Creating Multicomponent Materials with Polypeptides 6.4 Creating Multicomponent Materials Combining Polypeptides and Synthetic Polymers 6.4.1 Pros and Cons of Polypeptide-Based and Synthetic Polymer-Based Materials 6.4.2 Overarching Strategies for Designing Polypeptide-Synthetic Polymer Hybrids 6.4.3 Designing Inducible Systems Via Polypeptide-Synthetic Polymer Conjugation 6.4.4 Opportunities for Multicomponent Polypeptide/Protein-Synthetic Polymer Biomaterials in Bioengineering Applications 6.5 Creating Multicomponent Materials Combining Polypeptides and Nanoparticles 6.5.1 Multicomponent Materials Based on Polypeptides and Carbon Nanoparticles 6.5.2 Multicomponent Materials Based on Polypeptides and Inorganic Nanoparticles 6.6 Creating Multicomponent Materials Combining Polypeptides and Other Molecules 6.7 Conclusion and Outlook References Chapter 7: Chirality in Peptide Self-Assembly and Aggregation 7.1 Introduction 7.2 Pleated and Rippled β-Sheets 7.3 Helical Peptides 7.4 Cyclic Heterochiral Peptide Assemblies 7.5 Linear Heterochiral Peptide Assemblies 7.6 Inhibition of Amyloid Toxicity 7.7 Conclusion and Future Perspectives References Chapter 8: Characterization of Peptide-Based Nanomaterials 8.1 Introduction 8.2 Peptide Quality Control 8.3 Establishing Interactions in Peptide-Based Nanomaterials 8.3.1 Phase Diagrams and Titrations 8.3.2 Characterizing Peptide Interactions: Thermodynamics 8.3.2.1 Isothermal Titration Calorimetry 8.3.2.2 Differential Scanning Calorimetry 8.4 Spectroscopy 8.4.1 Fourier Transform Infrared Spectroscopy 8.4.2 Raman Spectroscopy 8.4.3 Circular Dichroism 8.4.4 Linear Dichroism 8.4.5 Nuclear Magnetic Resonance Spectroscopy 8.4.6 Fluorescence Spectroscopy Assays 8.5 Microscopy 8.5.1 Transmission and Scanning Electron Microscopies 8.5.2 Atomic Force Microscopy 8.5.3 Light Microscopy 8.6 Scattering 8.6.1 Small Angle Scattering 8.6.2 Small Angle Neutron Scattering (SANS) 8.6.3 X-Ray Powder Diffraction/Wide Angle X-Ray Scattering 8.6.4 Dynamic Light Scattering (DLS) and Zeta Potential 8.7 Rheology: Characterization of Viscoelasticity and Printability 8.8 Conclusions References Chapter 9: In Silico Prediction of Peptide Self-assembly into Nanostructures 9.1 Introduction 9.2 All-Atom MD Simulations 9.3 Coarse-Grain Simulations 9.4 Alternative Approaches 9.5 Conclusions and Perspectives References Chapter 10: Advanced Manufacturing of Peptide Nanomaterials 10.1 Introduction 10.2 Role of Microfluidics in Peptide Research 10.2.1 Peptide Incorporation into NP Shell 10.2.2 Peptide Encapsulation Within NP Shell 10.2.3 Other Uses of MFs in Peptide Research 10.3 Applications of Protein and Peptide Electrospun Nanofibres 10.3.1 Fundamentals of Electrospinning 10.3.2 Proteins and Peptides in Electrospinning 10.3.3 Applications of Protein and Peptides in Electrospinning 10.3.3.1 Drug Delivery 10.3.3.2 Tissue Engineering 10.3.3.3 Other Applications 10.4 Role of Additive Manufacturing in Peptide Research 10.4.1 Fused Deposition Modelling 10.4.2 Stereolithography and Digital Light Processing 10.4.3 Selective Laser Sintering (SLS) 10.4.4 Semi-solid Extrusion (EXT) 10.5 Conclusion and Future Directions References Chapter 11: Self-assembling Peptide Hydrogels as Extracellular Matrix-Mimicking Scaffolds for Tissue Regeneration in Chronic-D... 11.1 Introduction 11.2 The ECM: A Key Regulator of Tissues´ Biology 11.3 Functionalization of SAPHs to Direct Cell Biology 11.4 Musculoskeletal Tissue Diseases 11.4.1 Bone Diseases 11.4.2 Cartilage Diseases 11.5 Cardiovascular Diseases 11.5.1 Cardiovascular Diseases: SAPHs as Cardiac Molecules Depots for Heart Attack 11.5.2 Cardiovascular Diseases: SAPHs as Cellular Depots for Heart Attack 11.5.3 Cardiovascular Diseases: SAPHs as Cell-Load Depots for Other Cardiovascular Diseases Disorders 11.6 SAPHs for Principal Neurodegenerative Disorders 11.6.1 Neurodegenerative Disorders: SAPHs for Alzheimer´s Disease 11.6.2 Neurodegenerative Disorders: SAPHs for Parkinson´s Disease 11.6.3 NDs: SAPHs for Spinal Cord Injury 11.7 Pancreatic Diseases 11.7.1 Pancreatic Diseases: SAPHs as Vehicles for Islet Transplant 11.7.2 Pancreatic Diseases: SAPHs for Hyperglycemia and Wound Healing 11.8 Conclusion and Future Perspectives References Chapter 12: Peptide Nanostructured Materials as Drug Delivery Carriers 12.1 Introduction 12.1.1 Nanomaterials for Nanomedicine 12.1.2 Nanomaterials with Peptides for Medicine 12.1.3 Bioinspiration for Self-Assembling Nanomaterials 12.2 Proteins and Peptides as Building Blocks for Self-Assembled Biomaterials 12.2.1 From Natural Self-Assembling Proteins to Peptides 12.2.2 Minimalistic Peptides as Building Blocks for Supramolecular Biomaterials 12.2.3 Modern Peptide Therapeutics 12.3 Peptide Nanostructures for Drug Delivery 12.3.1 Physical Entrapment of Drugs 12.3.2 Non-covalent Drug Interactions 12.3.3 Covalent Drug Binding 12.4 Conclusions and Future Perspectives References Chapter 13: Peptide and Protein Emulsifiers 13.1 Introduction 13.2 Peptide Emulsifiers 13.2.1 Short Aromatic Peptide Emulsifiers 13.2.2 α-Helix Peptide Emulsifiers 13.2.3 β-Sheets Peptide Emulsifiers 13.2.4 Miscellaneous Surfactant-Like Peptides 13.3 Protein Emulsifiers 13.3.1 Milk Protein Emulsifiers 13.3.1.1 Caseins 13.3.1.2 Whey Proteins 13.3.2 Hydrophobins 13.3.3 Gelatin 13.3.4 Pea Proteins 13.4 Protein-Polysaccharide Mixed Emulsifiers 13.4.1 Protein-Polysaccharide Covalent Conjugates 13.4.2 Protein-Polysaccharide Physical Mixtures 13.5 Summary References Chapter 14: Antimicrobial Peptide Nanomaterials 14.1 Introduction 14.2 General Mechanisms of Antimicrobial Peptide Action 14.3 Self-Assembly 14.4 Nanotubes 14.5 Hydrogel-Forming Nanostructures 14.5.1 Surfactant-Like Peptides 14.5.2 Peptide Amphiphiles 14.5.3 Multidomain Peptides 14.5.4 β-Hairpin Peptides 14.6 Increasing In Vivo Longevity 14.6.1 d-α-Form Amino Acids 14.6.2 Other Peptidomimetics 14.6.3 Peptoids 14.7 Conclusions and Future Perspectives References Chapter 15: Multifunctional Peptide Biointerfaces 15.1 Introduction 15.2 Advantages of Multifunctional Peptide Biointerfaces 15.3 Origins of Modern Peptide Biointerfaces 15.3.1 The Fundamental Role of Antifouling Surfaces 15.3.2 Self-Assembled Monolayers (SAMs) and Thiol-Gold Surface Functionalization 15.3.3 Polysarcosine Peptoid Antifouling and the DOPA Universal Surface Adhesive 15.3.4 Protein Mimicry and Zwitterionic Glu-Lys (EK) Peptides 15.4 Multifunctional Peptides for Surface Functionalization 15.4.1 Direct Application of Bioactive Peptides 15.4.2 Linear SAM Designs 15.4.3 Non-linear Multifunctional Peptide Surface Designs 15.5 Conclusions References Chapter 16: Peptide Bionanomaterials Global Market: The Future of Emerging Industry 16.1 Introduction 16.2 Peptides as Bionanomaterials 16.3 Market Segments Based on Applications 16.3.1 Tissue Engineering and 3D Printing 16.3.2 Drug Delivery 16.3.3 Antibacterial Peptides for Wound Healing 16.3.4 Cosmetics 16.4 COVID-19 Impact on the Biomaterials Market 16.5 Market Comparisons 16.6 The Future for Peptide Bionanomaterials References