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新书资源(2009年5月)

Structure and function in cell signalling / John Nelson. — Chichester, England ; Hoboken, NJ : John Wiley & Sons, c2008. – (58.1483/N425)

Contents

    Contents
    
    Acknowledgments
    Preface
    1 The components and foundations of signalling
    1.1 Definition of terms used
    1.2 Historical foundations
    1.3 Early milestones in signal transduction research
    1.4 The discovery of receptors and G proteins
    1.5 cAMP pathways
    1.6 cAMP: ancient hunger signal - primitive signalling in amoebazoans and prokaryotes
    2 Enzymes and receptors - quantitative aspects
    2.1 Enzyme steady state assays - Michaelian enzymes
    2.2 Receptor equilibrium binding assays
    2.3 The receptor's environment
    2.4 Guanine nucleotides and the agonist 'affinity-shift' of 7-pass receptors
    3 Modules and motifs in transduction
    3.1 Src homology domains
    3.2 PH superfotd modules: PH-, PTB- and PDZ-domains
    3.3 Bcr-homology (BcrH) domains
    3.4 Dbl homology (DH) domains - partners of PH domains
    3.5 Bcl-2 homology (BH) domains
    3.6 Ras binding domains
    3.7 Phosphoserine/phosphothreonine-binding domains
    3.8 EF-hands - calcium-sensing modules
    3.9 CI and C2 domains - a Ca2+-activated, Lipid-binding, module
    References
    4 Protein kinase enzymes - activation and auto-inhibition
    4.1 The protein kinase fold
    4.2 Protein kinases activated by A-Loop phosphorytation
    4.3 The insulin receptor kinase (IRK) - a 'gated' kinase
    4.4 Cyctin dependent Kinases
    4.5 Secondary inhibition mechanisms - PKA
    5 7-pass receptors and the catabolic response
    5.1 7-pass receptor phylogeny
    5.2 Functional mechanisms of 7-pass receptors
    5.3 Amplification
    5.4 Adenylyl cyclase - signal limitation
    5.5 Adenylyt cyctase isoforms
    5.6 G proteins and the adenylyl cyclase erector isoforms
    5.7 Regulatory subunits of PKA and A-Kinase Anchoring Proteins
    5.8 PhosphoryLase kinase
    5.9 GLycogen phosphorytase
    5.10 Glycogen synthase
    5.11 Remaining questions - scaffolds and alternate second messenger 'receptors'
    5.12 G protein coupled receptor kinases - downregulators, signal integrators
    References
    6 Single pass growth factor receptors
    6.1 Receptor tyrosine kinases - Ugands and signal transduction
    6.2 The PDGFR family - signal transduction
    6.3 PDGFR family autoinhibition: juxtamembrane and A-loop tyrosines
    6.4 Crystal structure of kinase domain of PDGFR family-A member: Fit-3
    6.5 The ErbB family
    6.6 ErbB-type receptor signal transducUon particles
    6.7 Autoinhibition of EGFR and activation
    7 G proteins (I) - monomeric G proteins
    7.1 Classification
    7.2 ON and OFF states of Ras-like proteins
    7.3 Raf - a multi-domain serine/threonine kinase family of Ras effectors
    7.4 Ras protein structure and function
    7.5 The switch mechanism: hydrolysis-driven conformational change in Ras
    7.6 GTP hydrolysis
    7.7 Effector and regulator binding surfaces of Ras
    8 G proteins (II) - heterotrimeric G proteins
    8.1 CLassification and structural relationship with Ras
    8.2 Gα-subunits: the Ras-Like core, G-boxes and switch regions
    8.3 GTP exchange, hydrolysis and switch movements
    8.4 13/7- and receptor-binding surfaces of ~-subunits
    8.5 Modulators of G protein activity - the 'RGS' protein family
    8.6 Signal transduction by 13/y subunits
    9 The insulin receptor and the anabolic response
    9.1 The insulin receptor - a pre-dimerised RTK with a unique substrate
    9.2 InsR and IGF-IR: differentiation Leads differential tissue effects
    9.3 Features of metabolic control in key tissues
    9.4 InsR downstream signalling pathways
    9.5 The insulin receptor substrate - a surrogate signal transduction particle
    9.6 IRS-1/2 phosphorylation and PI-3-kinase activation
    9.7 Protein phosphatase-1 (PP-1)
    9.8 Insulin reverses effects of adrenaline and/or glucagon
    9.9 PIP3 downstream effects - glycogen synthesis
    9.10 Many questions remain
    10 Mitogens and cell cycle progression
    10.1 The mitogenic response and the cell division cycle
    10.2 GO, competency, and the point of no return in G1 - the 'R-point'
    10.3 Oncogene products derived from growth factor pathway components
    10.4 Transcription and cyclins
    10.5 Cyclin dependent Kinases
    10.6 Deactivation by cyclin destruction
    10.7 Cyclin dependent kinases - activation through cyclin synthesis
    10.8 Mitogenic pathway downstream of single pass tyrosine kinase receptors
    10.9 CyclinD/Cdk-4/6 - only important substrate is RB
    10.10 Retinoblastoma-related 'pocket proteins' - negative modulators of E2F
    10.11 De-repression of the cycLin E gene by cyclin D/Cdk-4/6
    10.12 Cyclin A/Cdk-2 - S-phase progression and termination
    10.13 The controlled process of mammalian DNA replication
    10.14 Cyclin B translocations and N-phase
    10.15 Cdk inhibitors
    10.16 p53 cell cycle arrest and apoptosis
    10.17 7-pass receptors and mitosis
    10.18 Concluding remarks and caveats
    Appendix 1: Worked examptes
    A.1 Enzyme and receptor assays worked out from raw data examples
    Appendix 2: RasMot: instattation and use
    Index