Time-resolved diffraction studies of muscle using synchrotron radiation

被引:29
作者
Harford, J [1 ]
Squire, J [1 ]
机构
[1] Univ London Imperial Coll Sci Technol & Med, Blackett Lab, Biophys Sect, London SW7 2BZ, England
关键词
D O I
10.1088/0034-4885/60/12/005
中图分类号
O4 [物理学];
学科分类号
0702 ;
摘要
Muscle contraction is one of those biological phenomena that we can all appreciate in our everyday lives. Sometimes it is when we are resting quietly and are aware of our heartbeat. At other times it may be when we are exerting ourselves and become short of breath, or when we exercise for a long period and our muscles start to ache. The way in which muscles produce force has exercised the minds of philosophers and scientists at least since the days of Erasistratus in the third century BC. Nowadays, of course, we know a very great deal about muscle structure, physiology and biochemistry, but we still do not know exactly what the molecular process is that produces movement. An ideal way of probing this process would be to be able to obtain signals from the relevant molecules as they actually go through their normal force-generating routine in an active muscle. The spatial dimensions involved are in the region of 1-50 nm, thus precluding the use of light microscopy, and the time regime is microseconds to milliseconds. Techniques with the appropriate spatial resolution might be electron microscopy and x-ray diffraction, but electron microscopy cannot yet be carried out on living tissue. X-ray diffraction methods can clearly have the right sort of spatial resolution, but what about recording diffraction patterns in the very short times involved (say 1 ms)? It is here that the high flux from synchrotron storage rings comes into its own. Using synchrotron radiation from, say, the SRS at the CCLRC Daresbury Laboratory it is possible to record x-ray diffraction patterns from living muscles in the millisecond time regime and to follow how these diffraction patterns change as the muscles go through typical contraction cycles. Unfortunately, x-ray diffraction is not a direct imaging method; the observed distribution: of diffracted intensity needs to be interpreted in some way to give useful information on the spatial relationships of the force-generating molecules. This review details the practical methods involved in recording time-resolved x-ray diffraction patterns from active muscles and the theoretical approaches that are being used to interpret the diffraction patterns that are obtained. The ultimate aim is to produce a series of time-sliced images of the changing molecular arrangements and shapes in the muscle as force is produced; together these images will form 'Muscle-The Movie'.
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页码:1723 / 1787
页数:65
相关论文
共 176 条
[1]   STRUCTURAL-CHANGES IN ACTIN-TROPOMYOSIN DURING MUSCLE REGULATION - COMPUTER MODELING OF LOW-ANGLE X-RAY-DIFFRACTION DATA [J].
ALKHAYAT, HA ;
YAGI, N ;
SQUIRE, JM .
JOURNAL OF MOLECULAR BIOLOGY, 1995, 252 (05) :611-632
[2]   DEVELOPMENT OF NON-INTENSIFIED CHARGE-COUPLED-DEVICE AREA X-RAY-DETECTORS [J].
ALLINSON, NM .
JOURNAL OF SYNCHROTRON RADIATION, 1994, 1 :54-62
[3]  
AMDT UW, 1994, SYNCHROTRON RAD BIOS, P388
[4]  
AMEMIYA Y, 1994, SYNCHROTRON RADIATION IN THE BIOSCIENCES, P395
[5]   LASER-STIMULATED LUMINESCENCE USED TO MEASURE X-RAY-DIFFRACTION OF A CONTRACTING STRIATED-MUSCLE [J].
AMEMIYA, Y ;
WAKABAYASHI, K ;
TANAKA, H ;
UENO, Y ;
MIYAHARA, J .
SCIENCE, 1987, 237 (4811) :164-168
[6]   DESIGN AND PERFORMANCE OF AN IMAGING PLATE SYSTEM FOR X-RAY-DIFFRACTION STUDY [J].
AMEMIYA, Y ;
MATSUSHITA, T ;
NAKAGAWA, A ;
SATOW, Y ;
MIYAHARA, J ;
CHIKAWA, J .
NUCLEAR INSTRUMENTS & METHODS IN PHYSICS RESEARCH SECTION A-ACCELERATORS SPECTROMETERS DETECTORS AND ASSOCIATED EQUIPMENT, 1988, 266 (1-3) :645-653
[7]  
Amemiya Y, 1991, Adv Biophys, V27, P115, DOI 10.1016/0065-227X(91)90012-3
[8]   IMAGING PLATE FOR TIME-RESOLVED X-RAY MEASUREMENTS [J].
AMEMIYA, Y ;
KISHIMOTO, S ;
MATSUSHITA, T ;
SATOW, Y ;
ANDO, M .
REVIEW OF SCIENTIFIC INSTRUMENTS, 1989, 60 (07) :1552-1556
[9]   3-DIMENSIONAL STRUCTURE DETERMINATION BY ELECTRON-MICROSCOPY OF TWO-DIMENSIONAL CRYSTALS [J].
AMOS, LA ;
HENDERSON, R ;
UNWIN, PNT .
PROGRESS IN BIOPHYSICS & MOLECULAR BIOLOGY, 1983, 39 (03) :183-231
[10]   RESULTS FROM THE 1ST USE OF MICROSTRIP GAS CHAMBERS IN A HIGH-ENERGY PHYSICS EXPERIMENT [J].
ANGELINI, F ;
BELLAZZINI, R ;
BREZ, A ;
DECAROLIS, G ;
MAGAZZU, C ;
MASSAI, MM ;
SPANDRE, G ;
TORQUATI, MR .
NUCLEAR INSTRUMENTS & METHODS IN PHYSICS RESEARCH SECTION A-ACCELERATORS SPECTROMETERS DETECTORS AND ASSOCIATED EQUIPMENT, 1992, 315 (1-3) :21-32