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1.
J Physiol ; 573(Pt 2): 305-28, 2006 Jun 01.
Article in English | MEDLINE | ID: mdl-16497718

ABSTRACT

Redevelopment of isometric force following shortening of skeletal muscle is thought to result from a redistribution of cross-bridge states. We varied the initial force and cross-bridge distribution by applying various length-change protocols to active skinned single fibres from rabbit psoas muscle, and observed the effect on the slowest phase of recovery ('late recovery') that follows transient changes. In response to step releases that reduced force to near zero ( approximately 8 nm (half sarcomere)(-1)) or prolonged shortening at high velocity, late recovery was well described by two exponentials of approximately equal amplitude and rate constants of approximately 2 s(-1) and approximately 9 s(-1) at 5 degrees C. When a large restretch was applied at the end of rapid shortening, recovery was accelerated by (1) the introduction of a slow falling component that truncated the rise in force, and (2) a relative increase in the contribution of the fast exponential component. The rate of the slow fall was similar to that observed after a small isometric step stretch, with a rate of 0.4-0.8 s(-1), and its effects could be reversed by reducing force to near zero immediately after the stretch. Force at the start of late recovery was varied in a series of shortening steps or ramps in order to probe the effect of cross-bridge strain on force redevelopment. The rate constants of the two components fell by 40-50% as initial force was raised to 75-80% of steady isometric force. As initial force increased, the relative contribution of the fast component decreased, and this was associated with a length constant of about 2 nm. The results are consistent with a two-state strain-dependent cross-bridge model. In the model there is a continuous distribution of recovery rate constants, but two-exponential fits show that the fast component results from cross-bridges initially at moderate positive strain and the slow component from cross-bridges at high positive strain.


Subject(s)
Isometric Contraction/physiology , Models, Biological , Muscle Fibers, Skeletal/physiology , Psoas Muscles/physiology , Animals , In Vitro Techniques , Male , Rabbits , Temperature
2.
Biophys J ; 87(2): 1112-35, 2004 Aug.
Article in English | MEDLINE | ID: mdl-15298915

ABSTRACT

Titin is responsible for the passive elasticity of the muscle sarcomere. The mechanical properties of skeletal and cardiac muscle titin were characterized in single molecules using a novel dual optical tweezers assay. Antibody pairs were attached to beads and used to select the whole molecule, I-band, A-band, a tandem-immunoglobulin (Ig) segment, and the PEVK region. A construct from the PEVK region expressing >25% of the full-length skeletal muscle isoform was chemically conjugated to beads and similarly characterized. By elucidating the elasticity of the different regions, we showed directly for the first time, to our knowledge, that two entropic components act in series in the skeletal muscle titin I-band (confirming previous speculations), one associated with tandem-immunoglobulin domains and the other with the PEVK region, with persistence lengths of 2.9 nm and 0.76 nm, respectively (150 mM ionic strength, 22 degrees C). Novel findings were: the persistence length of the PEVK component rose (0.4-2.7 nm) with an increase in ionic strength (15-300 mM) and fell (3.0-0.3 nm) with a temperature increase (10-60 degrees C); stress-relaxation in 10-12-nm steps was observed in the PEVK construct and hysteresis in the native PEVK region. The region may not be a pure random coil, as previously thought, but contains structured elements, possibly with hydrophobic interactions.


Subject(s)
Micromanipulation/methods , Molecular Motor Proteins/chemistry , Muscle Proteins/chemistry , Muscle, Skeletal/chemistry , Myocardium/chemistry , Protein Kinases/chemistry , Sarcomeres/chemistry , Animals , Connectin , Elasticity , Hydrogen-Ion Concentration , Muscle Proteins/analysis , Optics and Photonics , Physical Stimulation/methods , Protein Kinases/analysis , Rabbits , Stress, Mechanical , Temperature
3.
Brain Behav Evol ; 61(1): 28-44, 2003.
Article in English | MEDLINE | ID: mdl-12626860

ABSTRACT

The neocortex of primates contains several distinct neuron subtypes. Among these, Betz cells of primary motor cortex and Meynert cells of primary visual cortex are of particular interest for their potential role in specialized sensorimotor adaptations of primates. Betz cells are involved in setting muscle tone prior to fine motor output and Meynert cells participate in the processing of visual motion. We measured the soma volumes of Betz cells, Meynert cells, and adjacent infragranular pyramidal neurons in 23 species of primate and two species of non-primate mammal (Tupaia glis and Pteropus poliocephalus) using unbiased stereological techniques to examine their allometric scaling relationships and socioecological correlations. Results show that Betz somata become proportionally larger with increases in body weight, brain weight, and encephalization whereas Meynert somata remain a constant proportion larger than other visual pyramidal cells. Phylogenetic variance in the volumetric scaling of these neuronal subtypes might be related to species-specific adaptations. Enlargement of Meynert cells in terrestrial anthropoids living in open habitats, for example, might serve as an anatomical substrate for predator detection. Modification of the connectional and physiological properties of these neurons could constitute an important evolutionary mode for species-specific adaptation.


Subject(s)
Biological Evolution , Motor Cortex/anatomy & histology , Motor Cortex/cytology , Pyramidal Cells/cytology , Visual Cortex/anatomy & histology , Visual Cortex/cytology , Aged , Aged, 80 and over , Animals , Chiroptera , Humans , Neurons/cytology , Primates , Tupaia
4.
FEBS Lett ; 535(1-3): 55-60, 2003 Jan 30.
Article in English | MEDLINE | ID: mdl-12560078

ABSTRACT

Kettin is a high molecular mass protein of insect muscle associated with thin filaments and alpha-actinin in the Z-disc. It is thought to form a link between thin and thick filaments towards its C-terminus, contributing significantly to passive sarcomere stiffness. Here the elastic properties were characterised by mechanical stretches on an antibody-delimited region of the single molecule using two independent optical traps capable of exerting forces up to 150 pN. Step-like events were observed in the force-extension relationships consistent with the unfolding of Ig domains at moderate force and refolding of these domains at significantly higher forces than have been observed for related modular proteins.


Subject(s)
Drosophila Proteins , Infrared Rays , Insect Proteins/chemistry , Insect Proteins/radiation effects , Lasers , Muscle Proteins/chemistry , Muscle Proteins/radiation effects , Animals , Chemical Phenomena , Chemistry, Physical , Connectin , Drosophila , Elasticity/radiation effects , Hemiptera , Models, Biological , Monte Carlo Method , Protein Folding , Protein Structure, Tertiary/physiology , Protein Structure, Tertiary/radiation effects , Stress, Mechanical
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