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A Hitch-Hiker’s Guide to Molecular Thermodynamics What really makes proteins fold and ligands bind

A Hitch-Hiker’s Guide to Molecular Thermodynamics What really makes proteins fold and ligands bind. Alan Cooper. Chemistry Department Joseph Black Building, Glasgow University Glasgow G12 8QQ, Scotland. Amsterdam: November 2002. +. “C oncepts and tools for (medicinal) chemists”.

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A Hitch-Hiker’s Guide to Molecular Thermodynamics What really makes proteins fold and ligands bind

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  1. A Hitch-Hiker’s Guide to Molecular ThermodynamicsWhat really makes proteins fold and ligands bind Alan Cooper Chemistry Department Joseph Black Building, Glasgow University Glasgow G12 8QQ, Scotland Amsterdam: November 2002

  2. + “Concepts and tools for (medicinal) chemists” What makes this protein fold, and what controls its stability ?

  3. + “Concepts and tools for (medicinal) chemists” What makes this protein fold, and what controls its stability ? What are the thermodynamic forces responsible for ligand binding ? Can we use them to design better ligands ?

  4. “ Concepts and tools for medicinal chemists” Thermodynamic homeostasis, compensation; hydrogen-bonded lattices… ...the role of water in biomolecular interactions Microcalorimetry: analytical uses for biomolecular interactions and stability

  5. A bluffer’s guide to Thermodynamic Equilibrium… There is a natural tendency for all things (even atoms & molecules) to roll downhill - to fall to lower energy. H wants to be negative This is opposed (at the molecular level) by the equally natural tendency for thermal/Brownian motion (otherwise known as “entropy”) to make things go the other way… …and this effect gets bigger as the temperature increases. T.S wants to be positive

  6. Thermodynamic Equilibrium, expressed in terms of the Gibbs Free Energy change, reflects just the balance between these opposing tendencies… G = H - TS Equilibrium is reached when these two forces just balance (G = 0). The standard free energy change, G, is just another way of expressing the equilibrium constant, or affinity (K) for any process, on a logarithmic scale… G = -RTlnK

  7. Both enthalpy and entropy are integral functions of heat capacity... ….from which DG = DH - T.DS So DCp is the key - if we can understand heat capacity effects, then we can understand everything else.

  8. So, what is the role of water? So DCp is the key - if we can understand heat capacity effects, then we can understand everything else. And DCp is largely determined by the interactions between water and the macromolecule(s). In figure b many more waters are free than in a. And free waters are happy waters!

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