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1.
Biophys J ; 81(6): 3442-55, 2001 Dec.
Article in English | MEDLINE | ID: mdl-11721006

ABSTRACT

The structure of an early M-intermediate of the wild-type bacteriorhodopsin photocycle formed by actinic illumination at 230 K has been determined by x-ray crystallography to a resolution of 2.0 A. Three-dimensional crystals were trapped by illuminating with actinic light at 230 K, followed by quenching in liquid nitrogen. Amide I, amide II, and other infrared absorption bands, recorded from single bacteriorhodopsin crystals, confirm that the M-substate formed represents a structure that occurs early after deprotonation of the Schiff base. Rotation about the retinal C13-C14 double bond appears to be complete, but a relatively large torsion angle of 26 degrees is still seen for the C14-C15 bond. The intramolecular stress associated with the isomerization of retinal and the subsequent deprotonation of the Schiff base generates numerous small but experimentally measurable structural changes within the protein. Many of the residues that are displaced during the formation of the late M (M(N)) substate formed by three-dimensional crystals of the D96N mutant (Luecke et al., 1999b) are positioned, in early M, between their resting-state locations and the ones which they will adopt at the end of the M phase. The relatively small magnitude of atomic displacements observed in this intermediate, and the well-defined positions adopted by nearly all of the atoms in the structure, may make the formation of this structure favorable to model (simulate) by molecular dynamics.


Subject(s)
Bacteriorhodopsins/physiology , Light , Bacteriorhodopsins/chemistry , Binding Sites , Crystallography, X-Ray , Halobacterium/metabolism , Models, Molecular , Photochemistry , Protein Conformation , Protein Structure, Secondary , Spectroscopy, Fourier Transform Infrared , X-Ray Diffraction/instrumentation , X-Ray Diffraction/methods
2.
Ultramicroscopy ; 70(3): 107-13, 1998 Jan.
Article in English | MEDLINE | ID: mdl-9499588

ABSTRACT

A two-dimensional application specific integrated circuit (ASIC) based detector, designed for X-ray protein crystallography, has been tested to determine its suitability as a direct electron detector for TEM imaging in the voltage range of 20-400 keV. Several markedly different properties of this device distinguish it from the charge coupled device (CCD) detectors: (1) the ASIC detector can be used directly under electron bombardment in the voltage range stated above, therefore requiring no scintillator screen; (2) each active pixel of the device is an electron counter and generates digital output independently; (3) the readout of the device is frameless and event driven; (4) the device can be operated at the room temperature and is nearly noise free; and (5) the counting dynamic range of the device is virtually unlimited. It appears that an imaging system based on this type of device would be ideal for low-dose TEM imaging and online diffraction observation and recording, as well as more conventional imaging, providing the many advantages of direct digital readout for almost all applications.


Subject(s)
Crystallography, X-Ray/instrumentation , Microscopy, Electron/methods , Image Processing, Computer-Assisted , Proteins/analysis
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