Lecture 1

    Cards (22)

    • Structural motifs
      • Ring-finger motif, zinc-finger motif
    • Folding of proteins
      Aided by chaperones (cell machinery)
    • Transcriptional and translational complexes
      • Examples of cellular machines
    • Domains in proteins
      Regions of tertiary structure
    • Proteins in quaternary structure
      Modular and larger than structural motifs, can be structural or functional
    • Post-translational modifications
      • Phosphorylation, Ubiquitination
    • Energy requirements
      ATP: High energy phosphate bonds, energy currency of the cell; Energy released from ATP when terminal phosphate bond is broken
    • Functions of cellular machines
      Include target recognition, binding, linkers, scaffolds, etc
    • Allosteric Regulation mechanisms
      • Ca2+ interactions, The GTPase Switch
    • Functions of cellular machines
      Transcription, Translation, Protein folding, Transport, Protein degradation
    • Macromolecular complexes
      Multiple different protein components, very large, nano machines visible under electron microscopy
    • Units of proteins
      Daltons: Protein is measured in kDa, Protein complexes in MDa; Svedberg (Sv): Rate of sedimentation on a centrifuge, bigger it is → faster, greater Sv
    • Structural motifs
      Combinations of secondary structures determined by primary sequence
    • Assembly of macromolecular complexes
      Diverse modes of assembly around a core subunit, formation of subcomplexes prior to assembly
    • Dimerisation/oligomerisation
      Gives rise to quaternary structures
    • Heteromers
      Exist when different proteins come together
    • Protein synthesis
      Protein sequences encoded by genes (DNA) are translated from mRNA exported from the nucleus
    • Protein structure
      Primary structure → Secondary structure → Structural motifspartially folded intermediate structure → Tertiary structure → Quaternary structure
    • Regulation of cellular machines
      Turn them on and off through post-translational modifications, covalent modifications change protein structure with varied consequences
    • Advantages of multi-subunit cellular machines
      Adaptability in substrate recognition, flexibility, diversity in function and regulation
    • Allosteric Regulation
      Change in protein structure/function due to non-covalent binding by a ligand
    • Internal membranes
      Contain specialised protein machines and associated functions
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