GLORIA

GEOMAR Library Ocean Research Information Access

feed icon rss

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
  • 1
    Online Resource
    Online Resource
    La Vergne :Royal Society of Chemistry, The,
    Keywords: Proteins -- Analysis. ; Biosensors. ; Bioelectronics. ; Electronic books.
    Description / Table of Contents: The only book to focus on the generation of biosensing interfaces with analyses and control at the molecular level.
    Type of Medium: Online Resource
    Pages: 1 online resource (270 pages)
    Edition: 1st ed.
    ISBN: 9781847559777
    DDC: 547.7
    Language: English
    Note: Engineering the Bioelectronic Interface -- Contents -- Chapter 1 Communication with the Mononuclear Molybdoenzymes: Emerging Opportunities and Applications in Redox Enzyme Biosensors -- 1.1 Introduction - the Three Mo Enzyme Families -- 1.2 Mechanism -- 1.3 Amperometric Biosensors -- 1.4 Emerging Applications of Mo Enzymes in Sensing -- 1.4.1 Xanthine Oxidase Family -- 1.5 Sulfite Oxidase Family -- 1.5.1 Sulfite Oxidoreductase -- 1.6 DMSO Reductase Family -- 1.6.1 DMSO Reductase -- 1.6.2 Nitrate Reductase -- 1.6.3 Arsenite Oxidase -- 1.6.4 Chlorate and Perchlorate Reductase -- 1.7 Conclusions -- References -- Chapter 2 Scanning Probe Analyses at the Bioelectronic Interface -- 2.1 Introduction -- 2.1.1 Scanning Probe Microscopy -- 2.1.2 SPM Applications at the Biomolecular Interface -- 2.1.3 Summary -- 2.2 Bioelectronic Analyses -- 2.2.1 Electrode Surface Considerations -- 2.2.2 AFM Imaging Case Studies -- 2.2.3 The Direct Imaging of Electrochemistry and Enzyme Activity -- 2.2.4 Spectroscopic Assessment Electrodebiomolecule Electronic Coupling -- 2.3 Summary -- References -- Chapter 3 Electrical Interfacing of Redox Enzymes with Electrodes by Surface Reconstitution of Bioelectrocatalytic Nanostructures -- 3.1 Introduction -- 3.2 Reconstituted Enzyme Electrodes in Monolayer Configurations -- 3.3 Electrical Wiring of Redox Proteins with Electrodes by their Reconstitution on Cofactor-Functionalised Metallic Nanoparticles (NPs) or Carbon Nanotubes (CNTs) -- 3.4 Reconstitution of apo-Enzymes in Thin Films of Redox Polymers -- 3.5 Design of Electrically Contacted Enzyme Electrodes by the Crossing of Surface-confined Cofactor-enzyme Affinity Complexes -- 3.6 Reconstituted Enzyme Electrodes for Biofuel Cell Applications -- 3.7 Conclusions and Perspectives -- Acknowledgement -- References -- Chapter 4 Single-wall Carbon Nanotube Forests in Biosensors. , 4.1 Unique Properties of Carbon Nanotubes -- 4.1.1 Introduction -- 4.1.2 Electrocatalytic Properties -- 4.2 Biosensors Using Non-oriented Carbon Nanotube Electrodes -- 4.3 Biosensors Utilising Vertically Aligned Carbon Nanotube Forests -- 4.3.1 CNT Forest Fabrication -- 4.3.2 Biosensor Applications of SWNT Forests -- 4.4 Outlook for the Future -- References -- Chapter 5 Activating Redox Enzymes through Immobilisation and Wiring -- 5.1 Introduction -- 5.2 Protein Complexes -- 5.2.1 Co-crystallisation -- 5.2.2 Covalent Complexes -- 5.3 Electron Transfer at Electrodes -- 5.3.1 Voltammetry -- 5.3.2 Chronoamperometry -- 5.4 Surface Preparation -- 5.4.1 Carbon -- 5.4.2 Gold -- 5.4.3 Other Methods -- 5.5 Immobilisation -- 5.5.1 Direct Immobilisation -- 5.5.2 Wires -- 5.5.3 Wiring Proteins -- 5.6 Conclusion -- References -- Chapter 6 Cytochromes P450: Tailoring a Class of Enzymes for Biosensing -- 6.1 Introduction -- 6.2 Structure-function of Bacterial and Human Cytochromes P450 -- 6.3 The Need for Electrons: the Cytochrome P450 Catalytic Cycle -- 6.4 Human Cytochromes P450 and Drug Metabolism -- 6.5 Protein Engineering of P450s to Improve or Expand their Catalytic Properties -- 6.5.1 Directed Evolution of Cytochrome P450 Enzymes -- 6.5.2 Rational Design of Cytochrome P450 Enzymes -- 6.6 Interfacing Cytochromes P450 to Electrodes -- 6.6.1 Immobilisation on Unmodified Electrodes -- 6.6.2 Immobilisation with Surfactants, Polymers and Gold Nanoparticles -- 6.6.3 Immobilisation by Covalent Linkage on Gold Electrodes: Use of Spacers -- 6.6.4 Protein Engineering to Control Protein Immobilisation and Catalytic Turnover on Electrode Surfaces -- 6.7 Conclusions -- References -- Chapter 7 Label-free Field Effect Protein Sensing -- 7.1 Interfacial Protein Detection -- 7.2 Protein Microarrays -- 7.2.1 Array Substrates -- 7.2.2 Surface Chemistry and Immobilisation. , 7.2.3 Capture Biomolecules -- 7.2.4 Detection Tools -- 7.2.5 Ultrasensitive Protein Detection -- 7.3 Label-free Field Effect Protein Detection -- 7.3.1 Field Effect Transistor (FET) based Protein Sensing -- 7.3.2 Capacitance/Impedance Label-free Protein Sensing -- 7.3.3 Nanoscale Devices for Label-free Field Effect Protein Sensing -- 7.4 Conclusions -- References -- Chapter 8 Biological and Clinical Applications of Biosensors -- 8.1 Biosensing for Pure Biological Research -- 8.1.1 The Challenges of ''Omics'' and ''Systems'' Approaches -- 8.1.2 Biological Complexity -- 8.1.3 The Types of Device Required -- 8.2 Biosensing for Clinical Applications -- 8.2.1 The Clinical Problems - Diagnosis, Prognosis, Personalised Medicine -- 8.2.2 Biosensors for Clinical Applications -- 8.3 Further Reading -- References -- Subject Index.
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 2
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 27 (1989), S. 998-1001 
    ISSN: 0749-1581
    Keywords: Two-dimensional ; NMR ; Chemical shift ; Configuration ; Conformation ; Ganwuweizic acid ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Several two-dimensional NMR techniques were applied to assign completely the 1H and 13C chemical shifts and to study the configuration and conformation of a new triterpenoid, 3-keto-9,10,19-cyclopropyllanost-24-en-26-oic acid (ganwuweizic acid). Some 13C NMR signals previously reported for the triterpenoid skeleton were corrected.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 3
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 26 (1988), S. 1036-1037 
    ISSN: 0749-1581
    Keywords: Cephalotaxine ; 2D NMR ; 13C ; 1H assignments ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Prton and 13C chemical shift assignments have been made for naturally occurring cephalotaxine. The assignments of two carbons are reversed from those in the liteature. The chemical shifts and configurations of the pyrrolidine protons, aminomethylene protons and benzylic protons in cephalotaxine have been determined by the application of several 2D NMR techniques.
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...