The accuracy of structure factor phases determined from electron microscope images is determined mainly by the level of statistical significance, which is limited by the low level of allowed electron exposure and by the number of identical unit cells that can be averaged. It is shown here that Fourier transforms of small image fields of purple membrane (a two-dimensional crystal consisting of bacteriorhodopsin and endogenous lipids) can be combined to provide the same quality of phases as are obtained from Fourier transforms of large image fields of the same total area. Although Fourier transforms of such small image fields are statistically significant only at lower resolution, the data from many such image fields can be averaged at the ca...
Abstract Structure of membrane protiens can be determined by diffirent techniques.Electron Crystallo...
High Resolution three-dimensional (3D) reconstruction of several proteins has been achieved from two...
Several factors, including spatial and temporal coherence of the electron microscope, specimen movem...
The accuracy of structure factor phases determined from electron microscope images is determined mai...
A new method is described for analysing variations in structure from high resolution electron micros...
Electron crystallography determines the structure of membrane proteins and other periodic samples by...
Electron microscopy (EM) in combination with image analysis is a powerful technique to study protein...
SummaryIn electron crystallography, membrane protein structure is determined from two-dimensional cr...
Cryo-electron microscopy is a powerful technique employed by biophysicists in order to build highly ...
It is possible to determine the crystal structure of inorganic compounds to atomic resolution, by co...
Electron crystallography of two-dimensional (2D) crystals determines the structure of membrane prote...
The problem of crystal structure analysis at macromolecular resolution is tackled using notions borr...
Electron microscopy (EM) in combination with image analysis is a powerful technique to study protein...
High-resolution images of orthorhombic purple membrane have been obtained by electron cryomicroscopy...
A new criterion for the "useful " resolution of electron micrographs of macromolecular par...
Abstract Structure of membrane protiens can be determined by diffirent techniques.Electron Crystallo...
High Resolution three-dimensional (3D) reconstruction of several proteins has been achieved from two...
Several factors, including spatial and temporal coherence of the electron microscope, specimen movem...
The accuracy of structure factor phases determined from electron microscope images is determined mai...
A new method is described for analysing variations in structure from high resolution electron micros...
Electron crystallography determines the structure of membrane proteins and other periodic samples by...
Electron microscopy (EM) in combination with image analysis is a powerful technique to study protein...
SummaryIn electron crystallography, membrane protein structure is determined from two-dimensional cr...
Cryo-electron microscopy is a powerful technique employed by biophysicists in order to build highly ...
It is possible to determine the crystal structure of inorganic compounds to atomic resolution, by co...
Electron crystallography of two-dimensional (2D) crystals determines the structure of membrane prote...
The problem of crystal structure analysis at macromolecular resolution is tackled using notions borr...
Electron microscopy (EM) in combination with image analysis is a powerful technique to study protein...
High-resolution images of orthorhombic purple membrane have been obtained by electron cryomicroscopy...
A new criterion for the "useful " resolution of electron micrographs of macromolecular par...
Abstract Structure of membrane protiens can be determined by diffirent techniques.Electron Crystallo...
High Resolution three-dimensional (3D) reconstruction of several proteins has been achieved from two...
Several factors, including spatial and temporal coherence of the electron microscope, specimen movem...