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