Matching structural densities from different biophysical origins with gain and bias.

The registration of volumetric structures in real space involves geometric and density transformations that align a target map and a probe map in the best way possible. Many computational docking strategies exist for finding the geometric transformations that superimpose maps, but the problem of finding an optimal density transformation, for the purposes of difference calculations or segmentation, has received little attention in the literature. We report results based on simulated and experimental electron microscopy maps, showing that a single scale factor (gain) may be insufficient when it comes to minimizing the density discrepancy between an aligned target and probe. We propose an affine transformation, with gain and bias, that is parameterized by known surface isovalues and by an interactive centering of the "cancellation peak" in the surface thresholded difference map histogram. The proposed approach minimizes discrepancies across a wide range of interior densities. Owing to having only two parameters, it avoids overfitting and requires only minimal knowledge of the probe and target maps. The linear transformation also preserves phases and relative amplitudes in Fourier space. The histogram matching strategy was implemented in the newly revised volhist tool of the Situs package, version 2.6.

[1]  K. Taylor,et al.  Refined model of the 10S conformation of smooth muscle myosin by cryo-electron microscopy 3D image reconstruction. , 2003, Journal of molecular biology.

[2]  K Schulten,et al.  VMD: visual molecular dynamics. , 1996, Journal of molecular graphics.

[3]  D. DeRosier,et al.  Reconstruction of three-dimensional images from electron micrographs of structures with helical symmetry. , 1970, Journal of molecular biology.

[4]  Pablo Chacón,et al.  Using Situs for the registration of protein structures with low-resolution bead models from X-ray solution scattering , 2001 .

[5]  Zeyun Yu,et al.  A fast and adaptive method for image contrast enhancement , 2004, 2004 International Conference on Image Processing, 2004. ICIP '04..

[6]  Willy Wriggers,et al.  Three-dimensional reconstruction of tarantula myosin filaments suggests how phosphorylation may regulate myosin activity. , 2008, Journal of molecular biology.

[7]  K. Henrick,et al.  New electron microscopy database and deposition system. , 2002, Trends in biochemical sciences.

[8]  E P Morris,et al.  The structure of the acto-myosin subfragment 1 complex: results of searches using data from electron microscopy and x-ray crystallography. , 1997, Proceedings of the National Academy of Sciences of the United States of America.

[9]  P. Chacón,et al.  Multi-resolution contour-based fitting of macromolecular structures. , 2002, Journal of molecular biology.

[10]  Niels Volkmann,et al.  Evidence for cleft closure in actomyosin upon ADP release , 2000, Nature Structural Biology.

[11]  T S Baker,et al.  Low-resolution density maps from atomic models: how stepping "back" can be a step "forward". , 1999, Journal of structural biology.

[12]  Jorge Navaza,et al.  UROX 2.0: an interactive tool for fitting atomic models into electron-microscopy reconstructions , 2009, Acta crystallographica. Section D, Biological crystallography.

[13]  J. Frank Three-Dimensional Electron Microscopy of Macromolecular Assemblies , 2006 .

[14]  A. Roseman Docking structures of domains into maps from cryo-electron microscopy using local correlation. , 2000, Acta crystallographica. Section D, Biological crystallography.

[15]  W Wriggers,et al.  Modeling tricks and fitting techniques for multiresolution structures. , 2001, Structure.

[16]  Wei Zhang,et al.  Heterogeneity of large macromolecular complexes revealed by 3D cryo-EM variance analysis. , 2008, Structure.

[17]  Adrien Bartoli Direct Image Registration With Gain and Bias , 2006 .

[18]  Willy Wriggers,et al.  Using Situs for the integration of multi-resolution structures , 2010, Biophysical Reviews.

[19]  Conrad C. Huang,et al.  UCSF Chimera—A visualization system for exploratory research and analysis , 2004, J. Comput. Chem..