Multidomain assembled states of Hck tyrosine kinase in solution

An approach combining small-angle X-ray solution scattering (SAXS) data with coarse-grained (CG) simulations is developed to characterize the assembly states of Hck, a member of the Src-family kinases, under various conditions in solution. First, a basis set comprising a small number of assembly states is generated from extensive CG simulations. Second, a theoretical SAXS profile for each state in the basis set is computed by using the Fast-SAXS method. Finally, the relative population of the different assembly states is determined via a Bayesian-based Monte Carlo procedure seeking to optimize the theoretical scattering profiles against experimental SAXS data. The study establishes the concept of basis-set supported SAXS (BSS-SAXS) reconstruction combining computational and experimental techniques. Here, BSS-SAXS reconstruction is used to reveal the structural organization of Hck in solution and the different shifts in the equilibrium population of assembly states upon the binding of different signaling peptides.

[1]  John A. Tainer,et al.  Robust, high-throughput solution structural analyses by small angle X-ray scattering (SAXS) , 2009, Nature Methods.

[2]  S. Grzesiek,et al.  The solution structure of HIV-1 Nef reveals an unexpected fold and permits delineation of the binding surface for the SH3 domain of Hck tyrosine protein kinase , 1996, Nature Structural Biology.

[3]  Lee Makowski,et al.  A rapid coarse residue-based computational method for x-ray solution scattering characterization of protein folds and multiple conformational states of large protein complexes. , 2009, Biophysical journal.

[4]  B. Roux,et al.  Calculation of absolute protein-ligand binding free energy from computer simulations. , 2005, Proceedings of the National Academy of Sciences of the United States of America.

[5]  D. Fabbro,et al.  The crystal structure of a c-Src complex in an active conformation suggests possible steps in c-Src activation. , 2005, Structure.

[6]  Herbert Levine,et al.  Effective stochastic dynamics on a protein folding energy landscape. , 2006, The Journal of chemical physics.

[7]  Michele Vendruscolo,et al.  Structural biology. Dynamic visions of enzymatic reactions. , 2006, Science.

[8]  D. Kern,et al.  Dynamic personalities of proteins , 2007, Nature.

[9]  Friedrich Förster,et al.  Integration of small-angle X-ray scattering data into structural modeling of proteins and their assemblies. , 2008, Journal of molecular biology.

[10]  John Kuriyan,et al.  Crystal structure of the Src family tyrosine kinase Hck , 1997, Nature.

[11]  Greg L. Hura,et al.  Structure and flexibility within proteins as identified through small angle X-ray scattering. , 2009, General physiology and biophysics.

[12]  P. Pellicena,et al.  Src Phosphorylates Cas on Tyrosine 253 to Promote Migration of Transformed Cells* , 2003, Journal of Biological Chemistry.

[13]  J. Kuriyan,et al.  Activation of the Sire-family tyrosine kinase Hck by SH3 domain displacement , 1997, Nature.

[14]  Gerhard Hummer,et al.  Slow protein conformational dynamics from multiple experimental structures: the helix/sheet transition of arc repressor. , 2005, Structure.

[15]  J. Kuriyan,et al.  Crystal structure of Hck in complex with a Src family-selective tyrosine kinase inhibitor. , 1999, Molecular cell.

[16]  I. Kevrekidis,et al.  Coarse master equation from Bayesian analysis of replica molecular dynamics simulations. , 2005, The journal of physical chemistry. B.

[17]  Determinants of substrate recognition in nonreceptor tyrosine kinases. , 2003, Accounts of chemical research.

[18]  Robert G Parton,et al.  Observing Cell Surface Signaling Domains Using Electron Microscopy , 2003, Science's STKE.

[19]  Benoît Roux,et al.  Src Kinase Conformational Activation: Thermodynamics, Pathways, and Mechanisms , 2008, PLoS Comput. Biol..

[20]  Wendell A. Lim,et al.  The Structure and Function of Proline Recognition Domains , 2003, Science's STKE.

[21]  Benoît Roux,et al.  On the importance of a funneled energy landscape for the assembly and regulation of multidomain Src tyrosine kinases , 2007, Proceedings of the National Academy of Sciences.

[22]  Michele Vendruscolo,et al.  Dynamic Visions of Enzymatic Reactions , 2006, Science.

[23]  M. Blackledge,et al.  Structural characterization of flexible proteins using small-angle X-ray scattering. , 2007, Journal of the American Chemical Society.

[24]  Benoît Roux,et al.  Mapping the conformational transition in Src activation by cumulating the information from multiple molecular dynamics trajectories , 2009, Proceedings of the National Academy of Sciences.

[25]  Giulio Superti-Furga,et al.  Dynamic Coupling between the SH2 and SH3 Domains of c-Src and Hck Underlies Their Inactivation by C-Terminal Tyrosine Phosphorylation , 2001, Cell.

[26]  L. Johnson,et al.  Protein Kinase Inhibitors: Insights into Drug Design from Structure , 2004, Science.

[27]  G. Martin The hunting of the Src , 2001, Nature Reviews Molecular Cell Biology.

[28]  T. Smithgall,et al.  Activation of the Src Family Kinase Hck without SH3-Linker Release* , 2005, Journal of Biological Chemistry.

[29]  J. Kuriyan,et al.  Reciprocal regulation of Hck activity by phosphorylation of Tyr(527) and Tyr(416). Effect of introducing a high affinity intramolecular SH2 ligand. , 2000, The Journal of biological chemistry.

[30]  Greg L. Hura,et al.  X-ray solution scattering (SAXS) combined with crystallography and computation: defining accurate macromolecular structures, conformations and assemblies in solution. , 2011, Quarterly reviews of biophysics.

[31]  D. Svergun,et al.  Structural characterization of the active and inactive states of Src kinase in solution by small-angle X-ray scattering. , 2008, Journal of molecular biology.

[32]  D. Svergun,et al.  Small-angle scattering: a view on the properties, structures and structural changes of biological macromolecules in solution , 2003, Quarterly Reviews of Biophysics.

[33]  Sebastian Doniach,et al.  Small-angle X-ray scattering from RNA, proteins, and protein complexes. , 2007, Annual review of biophysics and biomolecular structure.

[34]  T. Smithgall,et al.  SH3-dependent stimulation of Src-family kinase autophosphorylation without tail release from the SH2 domain in vivo , 2002, Nature Structural Biology.

[35]  J. Kuriyan,et al.  High yield bacterial expression of active c‐Abl and c‐Src tyrosine kinases , 2005, Protein science : a publication of the Protein Society.