Title: Mammalian%20Muscle%20Properties
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2Mammalian Muscle Properties
Madden et al. IEEE J. Oceanic Engr. 29 706, 2004
3Skeletal muscle features
- Muscle surpasses artificial actuators only in the
fuel delivery - Linear actuation
- Adapted for intermittent duty and stiffness
(compliance) control - Versatile force control recruitment stiffness
modulation (w/o feedback)
Madden et al. IEEE J. Oceanic Engr. 29 706, 2004
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6Hill model Force dependence on contraction
velocity
7Motor Specific Power Ergs/s-g Force (dynes) Velocity mm/s
Actin Polymerization mtubule polymerization 109 108 10-7 10-7 1 .02
Myosin II Kinesin Spasmoneme 108 107 109 10-6 10-7 10-3 4 1 80,000
Car Striated muscle Bacterial Flagella Limulus aroscome Eukaryote Flagella Mitotic spindle 106 106 106 104 102 10-6 10-5 100 Hz 10 2
8McKibben muscle
9McK muscles
- Steel braid wrapped around a rubber tube.
- Crimped at ends
1020N/g
11Testing
12Antagonistic pairs for smooth torque
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14Friction in the mesh
- Filament on filament friction (no sliding
relative to the tube)
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17Properties of McK muscles
- 1. Fstatic CSA (pro2)
- 2. Fstatic P
- 3. Fstatic is independent of initial length
- 4. Fstatic max 1/ao
- 5. Fstatic 1/e
18Molecular Springs Ratchets
- Spasmoneme of the Vorticella
- Acrosome
- Actin polymerization
Mahdevan, L Science, 288 95, 2000.
19Spasmoneme of the Vorticella
20Actin Spring
- Acrosome needs to penetrate egg jelly.
- Spring is super-coiled- held twisted by scruin.
- Ca Ds scruin
21Supramolecular ratchets
- Pawl and ratchet analogy of actin polymerization
- How controlled? In quiescence, profilin is the
shut-off switch. Stimulus such as pH D in
presence of actin monomers can start. - Listeria rides this bus
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23Overall energy balance
24Conducting polymers
- Large molecular deformations (strains) induced by
current - Reversible Change in oxidation state
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32How does muscle fatigue?
- Test of a skinned muscle fiber from EDL of rat.
- Can activate by direct stimulation of any step in
the cascade.
Pederson, TH Science 305 1144, 2004
33F1 ATPase A rotary motor
- Can either make or break ATP, hence is reversible
- Torque of 40 pN-nM work in 1/3 rev. is 80 pn-nM
(40 2p/3) equivalent to free energy from ATP
hydrolysis - Can see rotation by attaching an actin filament
34Rotary Cellular Motors
- The rotary mechanism of ATP synthase , Stock D,
Gibbons C, Arechaga I, Leslie AGW, Walker
JECURRENT OPINION IN STRUCTURAL BIOLOGY ,10 (6)
672-679 DEC 2000 -
- 2. ATP synthase - A marvellous rotary engine of
the cell, Yoshida M, Muneyuki E, Hisabori
TNATURE REVIEWS MOLECULAR CELL BIOLOGY 2 (9)
669-677 SEP 2001 -
- 3. The gamma subunit in chloroplast F-1-ATPase
can rotate in a unidirectional and
counter-clockwise manner Hisabori T, Kondoh A,
Yoshida M FEBS LETTERS 463 (1-2) 35-38 DEC 10
1999 -
- 4. Constructing nanomechanical devices powered by
biomolecular motors.C. Montemagno, G Bachand,
Nanotechnology 10 225-2312, 1999.
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42Comparative motors
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47- When Lgtgt x, the chain has many bends and is
always crumpled in solution the FJC model
applies, with each link approximated as 2 x, and
perfectly flexible joints. - To count all possible curved states in a
smooth-bending rod in solution- its a WLC-
supercoiling is possible.
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49F1 ATPase A rotary motor
- Can either make or break ATP, hence is reversible
- Torque of 40 pN-nM work in 1/3 rev. is 80 pn-nM
(40 2p/3) equivalent to free energy from ATP
hydrolysis - Can see rotation by attaching an actin filament
50(www.sciencemag.org/feature/data/1049155.shl).
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