1 / 56

Flexible-Protein Docking

Flexible-Protein Docking. Dr Jonathan Essex School of Chemistry University of Southampton. Southampton. Programme. Existing small-molecule docking Typical approximations, and outcomes Evidence for receptor flexibility, and consequences

kineks
Télécharger la présentation

Flexible-Protein Docking

An Image/Link below is provided (as is) to download presentation Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author. Content is provided to you AS IS for your information and personal use only. Download presentation by click this link. While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server. During download, if you can't get a presentation, the file might be deleted by the publisher.

E N D

Presentation Transcript

  1. Flexible-Protein Docking Dr Jonathan Essex School of Chemistry University of Southampton

  2. Southampton

  3. Programme • Existing small-molecule docking • Typical approximations, and outcomes • Evidence for receptor flexibility, and consequences • Methods for accommodating protein flexibility in docking: • The ensemble approach • The induced fit approach

  4. Existing small-molecule docking • Taylor, R.D. et al. J. Comput. Aided Mol. Des.16, 151-166 (2002) • Many docking algorithms (some 127 references in this 2002 review!) • Most docking algorithms: • Rigid receptor hypothesis • Limited receptor flexibility in, for example, GOLD – polar hydrogens

  5. Existing small-molecule docking • Most docking algorithms: • Range of ligand sampling methods • Pattern matching, GA, MD, MC… • Treatment of intermolecular forces: • Simplified scoring functions: empirical, knowledge-based and molecular mechanics • Very simple treatment of solvation and entropy, or completely ignored!

  6. Existing small-molecule docking • And how well do they work? • Jones, G. et al. J. Mol. Biol.267, 727-748 (1997) • In re-docking studies, achieved a 71 % success rate • This is probably typical of most of these methods • So what’s missing?

  7. The scoring function • Existing functions inadequate • Too simplified, for reasons of computational expediency • Solvation and entropy often inadequately treated • Possible solutions? • More physics

  8. The rigid receptor hypothesis • Murray, C.W. et al. J. Comput. Aided Mol. Des.13, 547-562 (1999) • Docking to thrombin, thermolysin, and neuraminidase • PRO_LEADS – Tabu search • In self docking, ligand conformation correctly identified as the lowest energy structure – 76 % • For cross-docking – 49 % successful • Some of the associated protein movements very small

  9. The rigid receptor hypothesis • Erickson, J.A. et al. J. Med. Chem.47, 45-55 (2004) • Docking of trypsin, thrombin and HIV1-p • Self-docking, docking to a single structure that is closest to the average, and docking to apo structures • Docking accuracy declines on docking to the average structure, and is very poor for docking to apo • Decline in accuracy correlated with degree of protein movement

  10. The rigid receptor hypothesis • Erickson, J.A. et al. J. Med. Chem.47, 45-55 (2004)

  11. Models of Protein-Ligand Binding • Goh, C.-S. et al. Curr. Opin. Struct. Biol.14, 104-109 (2004) • Review of receptor flexibility for protein-protein interactions

  12. Models of Protein-Ligand Binding • This paper classifies protein-protein binding in terms of these models • Induced fit assumed if there is no experimental evidence for a pre-existing equilibrium of multiple conformations • Note that strictly this is an artificial distinction • Statistical mechanics – all states are accessible with a non-zero probability • For induced fit, probability of observing bound conformation without the ligand may be very small

  13. Protein flexibility in drug design • Teague, S.J. Nature Reviews2, 527-541 (2003) • Effect of ligand binding on free energy

  14. Protein flexibility in drug design • Multiple conformations of a few residues • Acetylcholinesterase • Phe330 flexible – acts as a swinging gate

  15. Protein flexibility in drug design • Movement of a large number of residues • Acetylcholinesterase (again!)

  16. Protein flexibility in drug design • Table 1 in Teague paper lists pharmaceutically relevant flexible targets (some 30 systems!) • Consequences of protein flexibility for ligand design • One site, several ligand binding modes possible

  17. Protein flexibility in drug design • Consequences • Allosteric inhibition • Binding often remote from active site – NNRTIs • Proteins in metabolism and transport • Promiscuous • Bind many compounds, in many orientations • E.g P450cam substrates, camphor versus thiocamphor (two orientations, different to camphor!)

  18. Experimental evidence for population shift • Binding kinetics • Binding to low-population conformation should yield slow kinetics – DGbarrier • Observed for p38 MAP kinase - mobile loop • Rates of association vary between 8.5 x 105 and 4.3 x 107 M-1s-1, depending on whether conformational change involved • Slow kinetics can make experimental comparison between assays difficult • Slow kinetics can improve ADME properties!

  19. Experimental evidence for population shift N-terminal receiver domain DNA binding domain Central catalytic domain Nitrogen Regulatory Protein C (NtrC) plays a central role in the bacterial metabolism of nitrogen

  20. Protein conformational change Phosphate Asp54 Changing nitrogen levels promote the activity of NtrB kinase NtrB kinase phosphorylates NtrC at aspartate 54 in the receiver domain

  21. Protein conformational change Phosphate Asp54 Phosphorylation promotes conformational change in the receiver domain

  22. NtrC – active and inactive conformations apparent P-NtrC – protein shifted towards activated conformation Volkman, B.F. et al.Science291, 2429-33 (2001) Protein conformational change

  23. Summary • Protein flexibility important in ligand design • Two basic mechanisms • Selection of a binding conformation from a pre-existing ensemble – population shift • Induced fit – binding to a previously unknown conformation • Thermodynamically, these mechanisms are identical • Evidence for population shift from binding kinetics, and protein NMR

  24. Docking methods for incorporating receptor flexibility • Ensemble docking • Docking to individual protein structures, or parts of protein structures – “ensemble docking” • Docking to a single average structure – “soft docking” • Induced fit modelling • Carlson, H.A. Curr. Opin. Chem. Biol.6, 447-452 (2002)

  25. Ensemble docking • Generate an ensemble of structures, and dock to them • Experimentally derived structures • NMR or X-ray structures • Computationally derived structures • Molecular dynamics • Simulated annealing • Normal mode propagation

  26. FlexE • Claussen, H. et al. J. Mol. Biol.308, 377-395 (2001) • Extension of the FlexX algorithm: • Preferred conformations for ligands identified • Simplified scoring function adopted – based on hydrogen bonds, ionic interactions etc. • Break ligand into base fragments by severing acyclic single bonds

  27. FlexE • Extension of the FlexX algorithm: • Base fragments placed in active site by superposing interaction centres • Incrementally reconstruct ligand onto base fragments • Test each partial solution and continue with the best for further reconstruction

  28. FlexE • United protein description • Use a set of protein structures representing flexibility, mutations, or alternative protein models • Assumes that overall shape of the protein and active site is maintained across the series • FlexE selects the combination of partial protein structures that best suit the ligand • Flexibility given by FlexE is therefore defined by the protein input structures

  29. FlexE • United protein description • Similar parts of the protein structures are merged • Dissimilar parts of the protein are treated as separate alternatives

  30. FlexE • United protein description • Some combinations of the structural features are incompatible and not considered • As the ligand is constructed, the optimum protein structure is identified • Combination strategy for the protein may result in a structure not present in the original data set

  31. FlexE • Evaluation • 10 proteins, 105 crystal structures • RMSD < 2.0 Å, within top ten solution, 67 % success • Cross-docking with FlexX gave 63 % • FlexE faster than cross-docking with FlexX • Aldose reductase - very flexible active site • FlexE docking successful (3 ligands) • Using only one rigid protein structure would not have worked

  32. Ensemble docking • Advantages: • Well-defined computational problem • Computational cost generally scales linearly with number of structures (potential combinatorial explosion) • Can use either experimental information, or structures derived from computation • Disadvantages: • What happens if the appropriate bound receptor conformation is not present in the ensemble?

  33. Soft-Docking • Knegtel, R.M.A. et al.J. Mol. Biol.266, 424-440 (1997) • Build interaction grids within DOCK that incorporate the effect of more than one protein structure • Effectively soften and average the different structures

  34. Soft-Receptor Modelling • Österberg, F. et al. Proteins46, 34-40 (2002) • Similar approach applied to Autodock grids • Energy-weighted grid • Boltzmann-type weighting applied to reduce the influence of repulsive terms • Combined grids performed very well – HIV protease

  35. Soft-Receptor Modelling

  36. Soft-Receptor Modelling • Advantages • Low computational cost – use of single averaged protein model • Can use experimental or simulation derived structures • Disadvantages • Cope with large-scale motion? • How reliable is this “averaged” representation? • Mutually exclusive binding regions could be simultaneously exploited • Active sites enlarged

  37. Induced-Fit Docking Methods • Allow protein conformational change at the same time as the docking proceeds • Taking some of these algorithms, in no particular order…

  38. Induced-Fit Docking Methods • Molecular dynamics methods: • Mangoni, R. et al. Proteins35, 153-162 (1999) • Separate thermal baths used for protein and ligand to facilitate sampling • Multicanonical molecular dynamics: • Nakajima, N. et al. Chem. Phys. Lett. 278, 297-301 (1997) • Bias normal molecular dynamics to yield a flat energy distribution

  39. Induced-Fit Docking Methods • Monte Carlo methods • Apostolakis, J. et al. J. Comput. Chem. 19, 21-37 (1998) • Hybrid Monte Carlo and minimisation method. Poisson-Boltzmann continuum solvation used • ICM, Abagyan, R. et al. J. Comput. Chem. 15, 488-506 (1997) • Conventional MC, plus side-chain moves from a rotamer library • Minimisation again required • VS - J. Mol. Biol.337, 209-225 (2004)

  40. Induced-Fit Docking Methods • FDS Taylor, R. et al.J. Comput. Chem.24, 1637-1656 (2003) • Flexible ligand/flexible protein docking • large side chain motions, rotamer library • Solvation included “on the fly” • continuum solvation model – GB/SA • Soft-core potential energy function • anneal the potential to improve sampling

  41. Rigid protein docking Low energy structures are essentially identical to the X-ray structure Dock starting from experimental result, does not return to it Arabinose Binding Protein

  42. Flexible protein docking Experimental structure found A number of other structures are isoenergetic Cannot uniquely identify the experimental structure Arabinose Binding Protein

  43. Flexible protein docking Most successful structure with experiment (transparent) Most successful structure, experiment, and isoenergetic mode Arabinose Binding Protein

  44. Monte Carlo Docking • 15 complexes studied • Rigid receptor • 13/15 identified X-ray binding mode • 8/15 were the unique, lowest energy structures • 3/15 were part of a cluster of low-energy binding modes • Flexible receptor • 11/15 identified X-ray binding mode • 3/15 were the unique, lowest energy structure • 6/15 were part of a cluster of low-energy binding modes

  45. FAB Fragment • Two isoenergetic binding modes Closest seed Isoenergetic seed

  46. Conclusion • Rigid protein docking as successful as other methods, but much more expensive • Flexible protein docking does find X-ray structures, but does not uniquely identify them • Refine scoring function? • Using this methodology, need to consider a number of structures • Further validation required

  47. Summary • Two main approaches for modelling receptor flexibility • Use of multiple structures (experimental or theoretical) either independently, or averaged in some way – ensemble approach • Allow the receptor to adopt conformations under the influence of the ligand – induced fit approach

  48. Summary • Ensemble is the more widely employed – less expensive, but limited somewhat by the composition of the ensemble • Induced fit should overcome this disadvantage of ensemble methods • Induced fit methods can have significant sampling problems • not computationally limited • search space large, and increasing as extra degrees of freedom added

  49. Flexible protein docking – a case study • Wei, B.Q. et al. J. Mol. Biol. 337, 1161-1182 (2004) • Use experimental structures • Like FlexE, flexible regions move independently, and are able to recombine • Modified version of DOCK used

  50. Flexible protein docking – a case study • Receptor decomposed into three parts • Green – rigid • Blue and red – two flexible parts • Ligand scored against each component • Best-fit protein conformation assembled from these components

More Related