Structural states of dictyostelium myosin
- 1 January 1979
- journal article
- research article
- Published by Wiley in Journal of Supramolecular Structure
- Vol. 12 (1) , 1-14
- https://doi.org/10.1002/jss.400120102
Abstract
Myosin purified from Dictyostelium amoebae has approximately 10% by weight of RNA associated with it, unless specific steps (DEAE cellulose chromatography or R Nase digestion) are taken to remove it. This RNA has significant effects on the structural states formed by the myosin at low ionic strength in the presence of Mg2+. Rapid precipitation of Rna-free myosin by dilution generates bipolar thick filaments (540 nm long, 33 nm thick), often with a bare zone and a 15-nm transverse repeat. Rapid precipitation of myosin with copurified RNA yields linear aggregates of bipolar filaments, showing some lateral association. Slow precipitation of RNA-free myosin by dialysis yields very long filaments or ribbons (>5 μm, 30–60 nm wide) in which the myosin may be packed diagonally across the filament, similar to the “side-polar” aggregates formed by other nonmuscle myosins and by smooth muscle myosin (Craig R, Megerman J: J Cell Biol 75:990, 1977; Hinssen H, D'Haese J, Small JV, Sobieszek A: J Ultrastruct Res 64:282, 1978). Slow precipitation of myosin with copurified RNA generates linear filaments with repeat intervals of 290 and 650 nm. Other polyanions were tested for their effects on myosin aggregation. Total RNA and ribosomal RNA from Dictyostelium, when added to RNA-free myosin, also induced the extensive linear aggregation seen with the copurified RNA/myosin complex, although higher concentrations of RNA were required to obtain quantitatively the same effect. DNA and heparin were also effective inducers of linear aggregation, whereas homopolymers of nucleotides and of acidic or basic amino acids were poorly effective.Keywords
This publication has 21 references indexed in Scilit:
- Mode of filament assembly of myosins from muscle and nonmuscle cellsJournal of Ultrastructure Research, 1978
- Assembly of smooth muscle myosin into side-polar filaments.The Journal of cell biology, 1977
- A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye bindingAnalytical Biochemistry, 1976
- Myosin from starfish egg: Properties and interaction with actinJournal of Molecular Biology, 1976
- Effects of RNase and RNA on in vitro aster assemblyJournal of Supramolecular Structure, 1976
- Purification of uterine myosin and synthetic filament formationJournal of Molecular Biology, 1974
- Biochemical and structural studies of actomyosin-like proteins from non-muscle cells: Isolation and characterization of myosin from amoebae of Dictyostelium discoideumJournal of Molecular Biology, 1974
- The contractile proteins of dictyostelium discoideumJournal of Supramolecular Structure, 1974
- Arrays of thick filaments in ATP-activated Amoeba model cellsExperimental Cell Research, 1970
- The low-angle X-ray diagram of vertebrate striated muscle and its behaviour during contraction and rigorJournal of Molecular Biology, 1967