Abstract
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.
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- Amos L. A., Henderson R., Unwin P. N. Three-dimensional structure determination by electron microscopy of two-dimensional crystals. Prog Biophys Mol Biol. 1982;39(3):183–231. doi: 10.1016/0079-6107(83)90017-2. [DOI] [PubMed] [Google Scholar]
- Amos L. A. Structure of muscle filaments studied by electron microscopy. Annu Rev Biophys Biophys Chem. 1985;14:291–313. doi: 10.1146/annurev.bb.14.060185.001451. [DOI] [PubMed] [Google Scholar]
- Bard F., Franzini-Armstrong C., Ip W. Rigor crossbridges are double-headed in fast muscle from crayfish. J Cell Biol. 1987 Nov;105(5):2225–2234. doi: 10.1083/jcb.105.5.2225. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Baumeister W., Barth M., Hegerl R., Guckenberger R., Hahn M., Saxton W. O. Three-dimensional structure of the regular surface layer (HPI layer) of Deinococcus radiodurans. J Mol Biol. 1986 Jan 20;187(2):241–250. doi: 10.1016/0022-2836(86)90231-7. [DOI] [PubMed] [Google Scholar]
- Bennett P. M. Decrease in section thickness on exposure to the electron beam; the use of tilted sections in estimating the amount of shrinkage. J Cell Sci. 1974 Aug;15(3):693–701. doi: 10.1242/jcs.15.3.693. [DOI] [PubMed] [Google Scholar]
- Berriman J., Leonard K. R. Methods for specimen thickness determination in electron microscopy. II. Changes in thickness with dose. Ultramicroscopy. 1986;19(4):349–366. doi: 10.1016/0304-3991(86)90095-1. [DOI] [PubMed] [Google Scholar]
- Bullard B., Leonard K., Larkins A., Butcher G., Karlik C., Fyrberg E. Troponin of asynchronous flight muscle. J Mol Biol. 1988 Dec 5;204(3):621–637. doi: 10.1016/0022-2836(88)90360-9. [DOI] [PubMed] [Google Scholar]
- Craig R., Szent-Györgyi A. G., Beese L., Flicker P., Vibert P., Cohen C. Electron microscopy of thin filaments decorated with a Ca2+-regulated myosin. J Mol Biol. 1980 Jun 15;140(1):35–55. doi: 10.1016/0022-2836(80)90355-1. [DOI] [PubMed] [Google Scholar]
- Egelman E. H., Francis N., DeRosier D. J. F-actin is a helix with a random variable twist. Nature. 1982 Jul 8;298(5870):131–135. doi: 10.1038/298131a0. [DOI] [PubMed] [Google Scholar]
- Egelman E. H., Francis N., DeRosier D. J. Helical disorder and the filament structure of F-actin are elucidated by the angle-layered aggregate. J Mol Biol. 1983 Jun 5;166(4):605–629. doi: 10.1016/s0022-2836(83)80286-1. [DOI] [PubMed] [Google Scholar]
- Elliott A., Offer G. Shape and flexibility of the myosin molecule. J Mol Biol. 1978 Aug 25;123(4):505–519. doi: 10.1016/0022-2836(78)90204-8. [DOI] [PubMed] [Google Scholar]
- Goody R. S., Holmes K. C. Cross-bridges and the mechanism of muscle contraction. Biochim Biophys Acta. 1983 Apr 15;726(1):13–39. doi: 10.1016/0304-4173(83)90009-5. [DOI] [PubMed] [Google Scholar]
- Goody R. S., Reedy M. C., Hofmann W., Holmes K. C., Reedy M. K. Binding of myosin subfragment 1 to glycerinated insect flight muscle in the rigor state. Biophys J. 1985 Feb;47(2 Pt 1):151–169. doi: 10.1016/s0006-3495(85)83889-3. [DOI] [PMC free article] [PubMed] [Google Scholar]
- HUXLEY A. F. Muscle structure and theories of contraction. Prog Biophys Biophys Chem. 1957;7:255–318. [PubMed] [Google Scholar]
- HUXLEY A. F., NIEDERGERKE R. Structural changes in muscle during contraction; interference microscopy of living muscle fibres. Nature. 1954 May 22;173(4412):971–973. doi: 10.1038/173971a0. [DOI] [PubMed] [Google Scholar]
- HUXLEY H., HANSON J. Changes in the cross-striations of muscle during contraction and stretch and their structural interpretation. Nature. 1954 May 22;173(4412):973–976. doi: 10.1038/173973a0. [DOI] [PubMed] [Google Scholar]
- Huxley H. E. The mechanism of muscular contraction. Science. 1969 Jun 20;164(3886):1356–1365. doi: 10.1126/science.164.3886.1356. [DOI] [PubMed] [Google Scholar]
- Kabsch W., Mannherz H. G., Suck D. Three-dimensional structure of the complex of actin and DNase I at 4.5 A resolution. EMBO J. 1985 Aug;4(8):2113–2118. doi: 10.1002/j.1460-2075.1985.tb03900.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kensler R. W., Stewart M. Frog skeletal muscle thick filaments are three-stranded. J Cell Biol. 1983 Jun;96(6):1797–1802. doi: 10.1083/jcb.96.6.1797. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lamvik M. K. Muscle thick filament mass measured by electron scattering. J Mol Biol. 1978 Jun 15;122(1):55–68. doi: 10.1016/0022-2836(78)90108-0. [DOI] [PubMed] [Google Scholar]
- Lovell S. J., Knight P. J., Harrington W. F. Fraction of myosin heads bound to thin filaments in rigor fibrils from insect flight and vertebrate muscles. Nature. 1981 Oct 22;293(5834):664–666. doi: 10.1038/293664a0. [DOI] [PubMed] [Google Scholar]
- Miller A., Tregear R. T. Structure of insect fibrillar flight muscle in the presence and absence of ATP. J Mol Biol. 1972 Sep 14;70(1):85–104. doi: 10.1016/0022-2836(72)90165-9. [DOI] [PubMed] [Google Scholar]
- Milligan R. A., Flicker P. F. Structural relationships of actin, myosin, and tropomyosin revealed by cryo-electron microscopy. J Cell Biol. 1987 Jul;105(1):29–39. doi: 10.1083/jcb.105.1.29. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Moore P. B., Huxley H. E., DeRosier D. J. Three-dimensional reconstruction of F-actin, thin filaments and decorated thin filaments. J Mol Biol. 1970 Jun 14;50(2):279–295. doi: 10.1016/0022-2836(70)90192-0. [DOI] [PubMed] [Google Scholar]
- Offer G., Couch J., O'Brien E., Elliott A. Arrangement of cross-bridges in insect flight muscle in rigor. J Mol Biol. 1981 Oct 5;151(4):663–702. doi: 10.1016/0022-2836(81)90429-0. [DOI] [PubMed] [Google Scholar]
- Offer G., Elliott A. Can a myosin molecule bind to two actin filaments? Nature. 1978 Jan 26;271(5643):325–329. doi: 10.1038/271325a0. [DOI] [PubMed] [Google Scholar]
- Otsuk I. Distribution of troponin components in the thin filament studied by immunoelectron microscopy. J Biochem. 1975 Mar;77(3):633–639. doi: 10.1093/oxfordjournals.jbchem.a130765. [DOI] [PubMed] [Google Scholar]
- Reedy M. K., Goody R. S., Hofmann W., Rosenbaum G. Co-ordinated electron microscopy and X-ray studies of glycerinated insect flight muscle. I. X-ray diffraction monitoring during preparation for electron microscopy of muscle fibres fixed in rigor, in ATP and in AMPPNP. J Muscle Res Cell Motil. 1983 Feb;4(1):25–53. doi: 10.1007/BF00711957. [DOI] [PubMed] [Google Scholar]
- Reedy M. K., Holmes K. C., Tregear R. T. Induced changes in orientation of the cross-bridges of glycerinated insect flight muscle. Nature. 1965 Sep 18;207(5003):1276–1280. doi: 10.1038/2071276a0. [DOI] [PubMed] [Google Scholar]
- Reedy M. K., Leonard K. R., Freeman R., Arad T. Thick myofilament mass determination by electron scattering measurements with the scanning transmission electron microscope. J Muscle Res Cell Motil. 1981 Mar;2(1):45–64. doi: 10.1007/BF00712061. [DOI] [PubMed] [Google Scholar]
- Reedy M. K., Reedy M. C. Rigor crossbridge structure in tilted single filament layers and flared-X formations from insect flight muscle. J Mol Biol. 1985 Sep 5;185(1):145–176. doi: 10.1016/0022-2836(85)90188-3. [DOI] [PubMed] [Google Scholar]
- Reedy M. K. Ultrastructure of insect flight muscle. I. Screw sense and structural grouping in the rigor cross-bridge lattice. J Mol Biol. 1968 Jan 28;31(2):155–176. doi: 10.1016/0022-2836(68)90437-3. [DOI] [PubMed] [Google Scholar]
- Squire J. M. General model of myosin filament structure. II. Myosin filaments and cross-bridge interactions in vertebrate striated and insect flight muscles. J Mol Biol. 1972 Dec 14;72(1):125–138. doi: 10.1016/0022-2836(72)90074-5. [DOI] [PubMed] [Google Scholar]
- Stokes D. L., DeRosier D. J. The variable twist of actin and its modulation by actin-binding proteins. J Cell Biol. 1987 Apr;104(4):1005–1017. doi: 10.1083/jcb.104.4.1005. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Taylor K. A., Amos L. A. A new model for the geometry of the binding of myosin crossbridges to muscle thin filaments. J Mol Biol. 1981 Apr 5;147(2):297–324. doi: 10.1016/0022-2836(81)90442-3. [DOI] [PubMed] [Google Scholar]
- Taylor K. A., Reedy M. C., Cordova L., Reedy M. K. Image reconstruction using electron micrographs of insect flight muscle. Use of thick transverse sections to supplement data from tilted thin longitudinal sections. Biophys J. 1986 Jan;49(1):353–364. doi: 10.1016/S0006-3495(86)83648-7. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Taylor K. A., Reedy M. C., Córdova L., Reedy M. K. Three-dimensional image reconstruction of insect flight muscle. II. The rigor actin layer. J Cell Biol. 1989 Sep;109(3):1103–1123. doi: 10.1083/jcb.109.3.1103. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Taylor K. A., Reedy M. C., Córdova L., Reedy M. K. Three-dimensional reconstruction of rigor insect flight muscle from tilted thin sections. 1984 Jul 26-Aug 1Nature. 310(5975):285–291. doi: 10.1038/310285a0. [DOI] [PubMed] [Google Scholar]
- Thomas D. D., Seidel J. C., Gergely J. Rotational dynamics of spin-labeled F-actin in the sub-millisecond time range. J Mol Biol. 1979 Aug 15;132(3):257–273. doi: 10.1016/0022-2836(79)90259-6. [DOI] [PubMed] [Google Scholar]
- Toyoshima C., Wakabayashi T. Three-dimensional image analysis of the complex of thin filaments and myosin molecules from skeletal muscle. IV. Reconstitution from minimal- and high-dose images of the actin-tropomyosin-myosin subfragment-1 complex. J Biochem. 1985 Jan;97(1):219–243. doi: 10.1093/oxfordjournals.jbchem.a135048. [DOI] [PubMed] [Google Scholar]
- Tregear R. T., Squire J. M. Myosin content and filament structure in smooth and striated muscle. J Mol Biol. 1973 Jun 25;77(2):279–290. doi: 10.1016/0022-2836(73)90336-7. [DOI] [PubMed] [Google Scholar]
- Vibert P., Craig R. Three-dimensional reconstruction of thin filaments decorated with a Ca2+-regulated myosin. J Mol Biol. 1982 May 15;157(2):299–319. doi: 10.1016/0022-2836(82)90236-4. [DOI] [PubMed] [Google Scholar]
- Vigers G. P., Crowther R. A., Pearse B. M. Three-dimensional structure of clathrin cages in ice. EMBO J. 1986 Mar;5(3):529–534. doi: 10.1002/j.1460-2075.1986.tb04242.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Walker M., Knight P., Trinick J. Negative staining of myosin molecules. J Mol Biol. 1985 Aug 5;184(3):535–542. doi: 10.1016/0022-2836(85)90300-6. [DOI] [PubMed] [Google Scholar]
- Walzthöny D., Bähler M., Eppenberger H. M., Wallimann T., Engel A. Unshadowed myosin molecules: STEM mass-maps of myosin heads. EMBO J. 1984 Nov;3(11):2621–2626. doi: 10.1002/j.1460-2075.1984.tb02183.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Wray J. S. Structure of the backbone in myosin filaments of muscle. Nature. 1979 Jan 4;277(5691):37–40. doi: 10.1038/277037a0. [DOI] [PubMed] [Google Scholar]
- Wray J., Vibert P., Cohen C. Actin filaments in muscle: pattern of myosin and tropomyosin/troponin attachments. J Mol Biol. 1978 Sep 25;124(3):501–521. doi: 10.1016/0022-2836(78)90184-5. [DOI] [PubMed] [Google Scholar]
- Yoshimura H., Nishio T., Mihashi K., Kinosita K., Jr, Ikegami A. Torsional motion of eosin-labeled F-actin as detected in the time-resolved anisotropy decay of the probe in the sub-millisecond time range. J Mol Biol. 1984 Nov 5;179(3):453–467. doi: 10.1016/0022-2836(84)90075-5. [DOI] [PubMed] [Google Scholar]