scholarly journals The Cross-Bridge Spring: Can Cool Muscles Store Elastic Energy?

Science ◽  
2013 ◽  
Vol 340 (6137) ◽  
pp. 1217-1220 ◽  
Author(s):  
N. T. George ◽  
T. C. Irving ◽  
C. D. Williams ◽  
T. L. Daniel
Keyword(s):  
Energy Storage ◽  
Elastic Energy ◽  
Molecular Motors ◽  
High Speed ◽  
Mechanical Energy ◽  
Elastic Strain Energy ◽  
Time Resolved ◽  
X Ray ◽  
Cross Bridge ◽  
Cross Bridges

Muscles not only generate force. They may act as springs, providing energy storage to drive locomotion. Although extensible myofilaments are implicated as sites of energy storage, we show that intramuscular temperature gradients may enable molecular motors (cross-bridges) to store elastic strain energy. By using time-resolved small-angle x-ray diffraction paired with in situ measurements of mechanical energy exchange in flight muscles of Manduca sexta, we produced high-speed movies of x-ray equatorial reflections, indicating cross-bridge association with myofilaments. A temperature gradient within the flight muscle leads to lower cross-bridge cycling in the cooler regions. Those cross-bridges could elastically return energy at the extrema of muscle lengthening and shortening, helping drive cyclic wing motions. These results suggest that cross-bridges can perform functions other than contraction, acting as molecular links for elastic energy storage.

scholarly journals Evidence for a vertebrate catapult: elastic energy storage in the plantaris tendon during frog jumping

2011 ◽  
Vol 8 (3) ◽  
pp. 386-389 ◽  
Author(s):  
Henry C. Astley ◽  
Thomas J. Roberts
Keyword(s):  
Energy Storage ◽  
Elastic Energy ◽  
High Speed ◽  
Angular Acceleration ◽  
Whole Body ◽  
Joint Motion ◽  
Joint Movement ◽  
Fascicle Length ◽  
Muscle Fascicle ◽  
Muscle Shortening

Anuran jumping is one of the most powerful accelerations in vertebrate locomotion. Several species are hypothesized to use a catapult-like mechanism to store and rapidly release elastic energy, producing power outputs far beyond the capability of muscle. Most evidence for this mechanism comes from measurements of whole-body power output; the decoupling of joint motion and muscle shortening expected in a catapult-like mechanism has not been demonstrated. We used high-speed marker-based biplanar X-ray cinefluoroscopy to quantify plantaris muscle fascicle strain and ankle joint motion in frogs in order to test for two hallmarks of a catapult mechanism: (i) shortening of fascicles prior to joint movement (during tendon stretch), and (ii) rapid joint movement during the jump without rapid muscle-shortening (during tendon recoil). During all jumps, muscle fascicles shortened by an average of 7.8 per cent (54% of total strain) prior to joint movement, stretching the tendon. The subsequent period of initial joint movement and high joint angular acceleration occurred with minimal muscle fascicle length change, consistent with the recoil of the elastic tendon. These data support the plantaris longus tendon as a site of elastic energy storage during frog jumping, and demonstrate that catapult mechanisms may be employed even in sub-maximal jumps.

scholarly journals Resting myosin cross-bridge configuration in frog muscle thick filaments.

1986 ◽  
Vol 102 (2) ◽  
pp. 610-618 ◽  
Author(s):  
M Cantino ◽  
J Squire
Keyword(s):  
Myosin Head ◽  
Freeze Fracture ◽  
Optical Diffraction ◽  
Outer Diameter ◽  
X Ray ◽  
Cross Bridge ◽  
Thick Filaments ◽  
Myosin Filaments ◽  
Cross Bridges ◽  
The Right

Clear images of myosin filaments have been seen in shadowed freeze-fracture replicas of single fibers of relaxed frog semitendinosus muscles rapidly frozen using a dual propane jet freezing device. These images have been analyzed by optical diffraction and computer averaging and have been modelled to reveal details of the myosin head configuration on the right-handed, three-stranded helix of cross-bridges. Both the characteristic 430-A and 140-150-A repeats of the myosin cross-bridge array could be seen. The measured filament backbone diameter was 140-160 A, and the outer diameter of the cross-bridge array was 300 A. Evidence is presented that suggests that the observed images are consistent with a model in which both of the heads of one myosin molecule tilt in the same direction at an angle of approximately 50-70 degrees to the normal to the filament long axis and are slewed so that they lie alongside each other and their radially projected density lies along the three right-handed helical tracks. Any perturbation of the myosin heads away from their ideal lattice sites needed to account for x-ray reflections not predicted for a perfect helix must be essentially along the three helical tracks of cross-bridges. Little trace of the presence of non-myosin proteins could be seen.

Deactivation rate and shortening velocity as determinants of contractile frequency

1990 ◽  
Vol 259 (2) ◽  
pp. R223-R230 ◽  
Author(s):  
R. L. Marsh
Keyword(s):  
Energy Storage ◽  
Elastic Energy ◽  
High Speed ◽  
Adductor Muscle ◽  
Stride Frequency ◽  
Kinetic Properties ◽  
Shortening Velocity ◽  
Thermal Dependence ◽  
Jet Propulsion

The kinetic properties of muscle that could influence locomotor frequency include rate of activation, rate of cross-bridge "attachment", intrinsic shortening velocity, and rate of deactivation. The latter two mechanisms are examined using examples from high-speed running in lizards and escape swimming in scallops. During running, inertial loading and elastic energy storage probably mitigate the effects of thermal alterations in intrinsic muscle shortening velocity. The result is a rather low thermal dependence of stride frequency over a 15-20 degree C temperature range. However, at lower temperatures, the longer times required for deactivation cause the thermal dependence of frequency to increase greatly. Scallops use a single muscle to swim by jet propulsion. In vivo shortening velocity in these animals also shows a low thermal dependence. As with high-speed running, the mechanics of jet propulsion may limit the effects of thermally induced changes in intrinsic shortening velocity. The largest thermal effect during swimming is on the initial phase of valve opening. The effects of temperature on the rate of deactivation of the adductor muscle could play an important role in limiting reextension of the muscle, which is dependent on elastic energy storage in the hinge ligament. These examples illustrate that the relative importance of various intrinsic contractile properties in controlling locomotor performance depends on the mechanics of the movements.

A quantum-limited CMOS-sensor-based high-speed imaging system for time-resolved x-ray scattering

2009 ◽  
Author(s):  
John Lowes ◽  
Chiao Liu ◽  
Sol M. Gruner ◽  
Brian Rodricks ◽  
Mark W. Tate ◽  
...  
Keyword(s):  
High Speed ◽  
Imaging System ◽  
High Speed Imaging ◽  
Time Resolved ◽  
X Ray ◽  
X Ray Scattering ◽  
Cmos Sensor ◽  
Ray Scattering

scholarly journals Elastic energy storage in the shoulder and the evolution of high-speed throwing in Homo

Nature ◽  
2013 ◽  
Vol 498 (7455) ◽  
pp. 483-486 ◽  
Author(s):  
Neil T. Roach ◽  
Madhusudhan Venkadesan ◽  
Michael J. Rainbow ◽  
Daniel E. Lieberman
Keyword(s):  
Energy Storage ◽  
Elastic Energy ◽  
High Speed

scholarly journals Pulse-resolved multi-photon X-ray detection at 31 MHz based on a quadrant avalanche photodiode

2014 ◽  
Vol 21 (4) ◽  
pp. 708-715 ◽  
Author(s):  
Tobias Reusch ◽  
Markus Osterhoff ◽  
Johannes Agricola ◽  
Tim Salditt
Keyword(s):  
High Speed ◽  
Single Photon ◽  
Photon Counting ◽  
Avalanche Photodiode ◽  
Single Photon Detection ◽  
Silicon Photodiode ◽  
Photon Detection ◽  
Time Resolved ◽  
Detection Scheme ◽  
X Ray

The technical realisation and the commissioning experiments of a high-speed X-ray detector based on a quadrant avalanche silicon photodiode and high-speed digitizers are described. The development is driven by the need for X-ray detectors dedicated to time-resolved diffraction and imaging experiments, ideally requiring pulse-resolved data processing at the synchrotron bunch repetition rate. By a novel multi-photon detection scheme, the exact number of X-ray photons within each X-ray pulse can be recorded. Commissioning experiments at beamlines P08 and P10 of the storage ring PETRA III, at DESY, Hamburg, Germany, have been used to validate the pulse-wise multi-photon counting scheme at bunch frequencies ≥31 MHz, enabling pulse-by-pulse readout during the PETRA III 240-bunch mode with single-photon detection capability. An X-ray flux of ≥3.7 × 109 photons s−1can be detected while still resolving individual photons at low count rates.

scholarly journals 3L1345 High-speed time-resolved X-ray diffraction study of the structural changes of contractile proteins induced by the photolysis of caged-ATP

2002 ◽  
Vol 42 (supplement2) ◽  
pp. S187
Author(s):  
J. Wakayama ◽  
T. Tamura ◽  
K. Inoue ◽  
T. Oka ◽  
N. Yagi ◽  
...  
Keyword(s):  
Diffraction Study ◽  
High Speed ◽  
Structural Changes ◽  
Contractile Proteins ◽  
X Ray Diffraction ◽  
Time Resolved ◽  
X Ray ◽  
Caged Atp

scholarly journals Thermal behavior of single-crystal scintillators for high-speed X-ray imaging

2019 ◽  
Vol 26 (1) ◽  
pp. 205-214 ◽  
Author(s):  
Alan Kastengren
Keyword(s):  
Single Crystal ◽  
High Speed ◽  
Thermal Loading ◽  
Indirect Detection ◽  
X Rays ◽  
Time Resolved ◽  
X Ray ◽  
Damage And Failure ◽  
Light Levels ◽  
X Ray Imaging

Indirect detection of X-rays using single-crystal scintillators is a common approach for high-resolution X-ray imaging. With the high X-ray flux available from synchrotron sources and recent advances in high-speed visible-light cameras, these measurements are increasingly used to obtain time-resolved images of dynamic phenomena. The X-ray flux on the scintillator must, in many cases, be limited to avoid thermal damage and failure of the scintillator, which in turn limits the obtainable light levels from the scintillator. In this study, a transient one-dimensional numerical simulation of the temperature and stresses within three common scintillator crystals (YAG, LuAG and LSO) used for high-speed X-ray imaging is presented. Various conditions of thermal loading and convective cooling are also presented.

scholarly journals Effect of Active Lengthening and Shortening on Small-Angle X-ray Reflections in Skinned Skeletal Muscle Fibres

2021 ◽  
Vol 22 (16) ◽  
pp. 8526
Author(s):  
Venus Joumaa ◽  
Ian C. Smith ◽  
Atsuki Fukutani ◽  
Timothy R. Leonard ◽  
Weikang Ma ◽  
...  
Keyword(s):  
Steady State ◽  
Small Angle ◽  
Isometric Contraction ◽  
Sarcomere Length ◽  
Force Enhancement ◽  
X Ray ◽  
Cross Bridge ◽  
Residual Force ◽  
Residual Force Enhancement ◽  
Cross Bridges

Our purpose was to use small-angle X-ray diffraction to investigate the structural changes within sarcomeres at steady-state isometric contraction following active lengthening and shortening, compared to purely isometric contractions performed at the same final lengths. We examined force, stiffness, and the 1,0 and 1,1 equatorial and M3 and M6 meridional reflections in skinned rabbit psoas bundles, at steady-state isometric contraction following active lengthening to a sarcomere length of 3.0 µm (15.4% initial bundle length at 7.7% bundle length/s), and active shortening to a sarcomere length of 2.6 µm (15.4% bundle length at 7.7% bundle length/s), and during purely isometric reference contractions at the corresponding sarcomere lengths. Compared to the reference contraction, the isometric contraction after active lengthening was associated with an increase in force (i.e., residual force enhancement) and M3 spacing, no change in stiffness and the intensity ratio I1,1/I1,0, and decreased lattice spacing and M3 intensity. Compared to the reference contraction, the isometric contraction after active shortening resulted in decreased force, stiffness, I1,1/I1,0, M3 and M6 spacings, and M3 intensity. This suggests that residual force enhancement is achieved without an increase in the proportion of attached cross-bridges, and that force depression is accompanied by a decrease in the proportion of attached cross-bridges. Furthermore, the steady-state isometric contraction following active lengthening and shortening is accompanied by an increase in cross-bridge dispersion and/or a change in the cross-bridge conformation compared to the reference contractions.

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