Cryogenic electron microscopy (cryo-EM) provides a unique opportunity to study the structural heterogeneity of biomolecules. Being able to explain this heterogeneity with atomic models would help our understanding of their functional mechanisms but the size and ruggedness of the structural space (the space of atomic 3D cartesian coordinates) presents an immense challenge. Here, we describe a heterogeneous reconstruction method based on an atomistic representation whose deformation is reduced to a handful of collective motions through normal mode analysis. Our implementation uses an autoencoder. The encoder jointly estimates the amplitude of motion along the normal modes and the 2D shift between the center of the image and the center of the ...
Proteins and other biomolecules form dynamic macromolecular machines that carry out essential biolog...
© 2014 John Wiley & Sons, Ltd. Cryo-electron microscopy is a powerful technique for the determinatio...
SummaryA novel method to flexibly fit atomic structures into electron microscopy (EM) maps using mol...
We consider the problem of recovering the three-dimensional atomic structure of a flexible macromole...
Macromolecules change their shape (conformation) in the process of carrying out their functions. The...
Cryo-electron microscopy (cryo-EM) is unique among tools in structural biology in its ability to ima...
Cryogenic electron microscopy is widely used in structural biology, but its resolution is often limi...
We present a correlation-driven molecular dynamics (CDMD) method for automated refinement of atomist...
Cryo-electron microscopy (cryo-EM) has become a tool of fundamental importance in structural biology...
Abstract An explosion of new data from high-resolution cryo-electron microscopy (cryo-EM) studies ha...
Background: Dramatic progress has recently been made in cryo-electron microscopy technologies, which...
Abstract An explosion of new data from high-resolution cryo-electron microscopy (cryo-EM) studies ha...
International audienceDensity volumes obtained by three-dimensional reconstruction of biomolecular c...
The major goal of this manuscript is to create a procedure to model the ensemble of conformations pr...
Single particle cryo-electron microscopy has become a critical tool in structural biology over the l...
Proteins and other biomolecules form dynamic macromolecular machines that carry out essential biolog...
© 2014 John Wiley & Sons, Ltd. Cryo-electron microscopy is a powerful technique for the determinatio...
SummaryA novel method to flexibly fit atomic structures into electron microscopy (EM) maps using mol...
We consider the problem of recovering the three-dimensional atomic structure of a flexible macromole...
Macromolecules change their shape (conformation) in the process of carrying out their functions. The...
Cryo-electron microscopy (cryo-EM) is unique among tools in structural biology in its ability to ima...
Cryogenic electron microscopy is widely used in structural biology, but its resolution is often limi...
We present a correlation-driven molecular dynamics (CDMD) method for automated refinement of atomist...
Cryo-electron microscopy (cryo-EM) has become a tool of fundamental importance in structural biology...
Abstract An explosion of new data from high-resolution cryo-electron microscopy (cryo-EM) studies ha...
Background: Dramatic progress has recently been made in cryo-electron microscopy technologies, which...
Abstract An explosion of new data from high-resolution cryo-electron microscopy (cryo-EM) studies ha...
International audienceDensity volumes obtained by three-dimensional reconstruction of biomolecular c...
The major goal of this manuscript is to create a procedure to model the ensemble of conformations pr...
Single particle cryo-electron microscopy has become a critical tool in structural biology over the l...
Proteins and other biomolecules form dynamic macromolecular machines that carry out essential biolog...
© 2014 John Wiley & Sons, Ltd. Cryo-electron microscopy is a powerful technique for the determinatio...
SummaryA novel method to flexibly fit atomic structures into electron microscopy (EM) maps using mol...