Small-Angle X-ray Diffraction of Muscle Using Undulator Radiation from the Tristan Main Ring at KEK

Time-resolved X-ray diffraction of muscle has demanded ever-increasing flux into small sample volumes with low beam divergence. Results are reported of static and time-resolved small-angle X-ray diffraction studies on muscle fibers using a hard X-ray undulator installed in the Tristan main ring at K...

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Veröffentlicht in:Journal of synchrotron radiation. - 1994. - 3(1996), Pt 6 vom: 01. Nov., Seite 305-12
1. Verfasser: Yagi, N (VerfasserIn)
Weitere Verfasser: Wakabayashi, K, Iwamoto, H, Horiuti, K, Kojima, I, Irving, T C, Takezawa, Y, Sugimoto, Y, Iwamoto, S, Majima, T, Amemiya, Y, Ando, M
Format: Aufsatz
Sprache:English
Veröffentlicht: 1996
Zugriff auf das übergeordnete Werk:Journal of synchrotron radiation
Schlagworte:Journal Article
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245 1 0 |a Small-Angle X-ray Diffraction of Muscle Using Undulator Radiation from the Tristan Main Ring at KEK 
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520 |a Time-resolved X-ray diffraction of muscle has demanded ever-increasing flux into small sample volumes with low beam divergence. Results are reported of static and time-resolved small-angle X-ray diffraction studies on muscle fibers using a hard X-ray undulator installed in the Tristan main ring at KEK, Tsukuba, Japan, as an innovative source of synchrotron radiation more intense and better collimated than that available with the Photon Factory bending-magnet beamline. Static studies used the low divergence of the source to obtain detailed high-quality diffraction patterns of stable muscle states. The diffraction patterns from live skeletal muscles showed the numerous (over 100) meridional reflections. The well collimated beam from the undulator made it possible to clearly resolve, with an angular resolution of ca 700 nm, the closely spaced diffraction peaks arising from the two halves of the thick filaments centred on the M lines in a sarcomere, in addition, the diffraction peaks from the thin filaments on opposite sides of the Z bands could be resolved with an angular resolution of ca 1000 nm. The detailed structure of the meridional pattern defines the nature of the molecular packing in the thick and thin filaments. Time-resolved experiments using a focusing mirror aimed to prove cross-bridge states in striated muscle fibers by collecting X-ray diffraction data at a 0.185 ms time resolution from sinusoidally oscillating chemically skinned rabbit muscle fibers during active contraction and in rigor. When sinusoidal length changes at 500 Hz with a peak-to-peak amplitude of 0.6% of the muscle length were applied to a small fiber bundle, the tension showed a simple elastic response during the length oscillation. In the active muscle the intensity of the 14.5 nm myosin-based meridional reflection changed out of phase with the tension change during the oscillating length change. In contrast, in the rigor muscle it occurred in phase with the tension change. The high time-resolved experiments provide an insight into the coupling between conformational changes and force generation of the actomyosin cross-bridges. These studies provide a preview of the expected gains for muscle studies from the more widespread use of undulator radiation at third-generation synchrotron sources 
650 4 |a Journal Article 
700 1 |a Wakabayashi, K  |e verfasserin  |4 aut 
700 1 |a Iwamoto, H  |e verfasserin  |4 aut 
700 1 |a Horiuti, K  |e verfasserin  |4 aut 
700 1 |a Kojima, I  |e verfasserin  |4 aut 
700 1 |a Irving, T C  |e verfasserin  |4 aut 
700 1 |a Takezawa, Y  |e verfasserin  |4 aut 
700 1 |a Sugimoto, Y  |e verfasserin  |4 aut 
700 1 |a Iwamoto, S  |e verfasserin  |4 aut 
700 1 |a Majima, T  |e verfasserin  |4 aut 
700 1 |a Amemiya, Y  |e verfasserin  |4 aut 
700 1 |a Ando, M  |e verfasserin  |4 aut 
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