
Isolated troponin-tropomyosin complex from Lethocerus indicus asynchronous flight muscle forms paracrystals on a positively charged lipid monolayer. Single particle analysis was carried out on individual complexes selected from electron micrographs of negatively stained paracrystals. By a combination of correlation and classification techniques, different average projections of the object were obtained. An initial three-dimensional model was calculated by determining the Euler angles for the different views using a common line approach. This starting model was then used as a reference for the further three-dimensional refinement of the model using the original data set. The refined model of the troponin complex has a diameter of approximately 90 A and a volume corresponding with a molecular mass of about 120 kDa for the globular domain. The resolution of the reconstruction was determined to be 32 A using the differential phase residual method and 26 A using the Fourier shell correlation criterion.
Models, Molecular, Macromolecular Substances, Protein Conformation, Tropomyosin, Troponin, Hemiptera, Molecular Weight, Membrane Lipids, Microscopy, Electron, Flight, Animal, Image Processing, Computer-Assisted, Animals, Insect Proteins, Crystallization, Muscle, Skeletal
Models, Molecular, Macromolecular Substances, Protein Conformation, Tropomyosin, Troponin, Hemiptera, Molecular Weight, Membrane Lipids, Microscopy, Electron, Flight, Animal, Image Processing, Computer-Assisted, Animals, Insect Proteins, Crystallization, Muscle, Skeletal
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