Cross-bridge interaction, with oppositely polarized actin filaments in double-overlap zones of insect flight muscle

Nature ◽  
1984 ◽  
Vol 309 (5964) ◽  
pp. 168-170 ◽  
Author(s):  
K. TrombitÁs ◽  
A. Tigyi-Sebes
1989 ◽  
Vol 109 (3) ◽  
pp. 1085-1102 ◽  
Author(s):  
K A Taylor ◽  
M C Reedy ◽  
L Córdova ◽  
M K Reedy

We have obtained detailed three-dimensional images of in situ cross-bridge structure in insect flight muscle by electron microscopy of multiple tilt views of single filament layers in ultrathin sections, supplemented with data from thick sections. In this report, we describe the images obtained of the myac layer, a 25-nm longitudinal section containing a single layer of alternating myosin and actin filaments. The reconstruction reveals averaged rigor cross-bridges that clearly separate into two classes constituting lead and rear chevrons within each 38.7-nm axial repeat. These two classes differ in tilt angle, size and shape, density, and slew. This new reconstruction confirms our earlier interpretation of the lead bridge as a two-headed cross-bridge and the rear bridge as a single-headed cross-bridge. The importance of complementing tilt series with additional projections outside the goniometer tilt range is demonstrated by comparison with our earlier myac layer reconstruction. Incorporation of this additional data reveals new details of rigor cross-bridge structure in situ which include clear delineation of (a) a triangular shape for the lead bridge, (b) a smaller size for the rear bridge, and (c) density continuity across the thin filament in the lead bridge. Within actin's regular 38.7-nm helical repeat, local twist variations in the thin filament that correlate with the two cross-bridge classes persist in this new reconstruction. These observations show that in situ rigor cross-bridges are not uniform, and suggest three different myosin head conformations in rigor.


2004 ◽  
Vol 86 (5) ◽  
pp. 3009-3019 ◽  
Author(s):  
Richard T. Tregear ◽  
Mary C. Reedy ◽  
Yale E. Goldman ◽  
Kenneth A. Taylor ◽  
Hanspeter Winkler ◽  
...  

1966 ◽  
Vol 1 (1) ◽  
pp. 49-57
Author(s):  
D. S. SMITH ◽  
B. L. GUPTA ◽  
UNA SMITH

The cytological organization of three insect visceral muscles has been examined in the electron microscope. In each instance, the fibres were found to be striated, and the striation pattern has been shown to reflect the distribution along the sarcomere of two sets of myofilaments. In transverse sections of the fibre at the level of the A band, these muscles have been found to exhibit an unusual myofilament array in which each thick (myosin) filament is surrounded by twelve thin (actin) filaments rather than six, as in insect flight muscle and vertebrate skeletal muscle. The distribution of T-system tubules and cisternae of the sarcoplasmic reticulum in these visceral fibres is described, and compared with the corresponding membrane systems in other striated muscles.


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