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Chemomechanics

The equipment for the slit-film fiber process is shown in Figure 15 (29). An olefin film is cast, and as in melt spinning, the morphology and composition of the film determine the processing characteristics. Fibers may be produced by cutting or slitting the film, or by chemomechanical fibrillation. [Pg.319]

Gopal, D., Pavlov, D. I., Levitsky, D. I., et al., 1996. Chemomechanical trans-dnction in the actomyosin molecnlar motor by 2, 3 -dideoxydidehydro-ATP and characterizadon of its interacdon with myosin snbfragment 1 in die presence and absence of acdn. Biochemistry 35 10149-10157. [Pg.564]

Osada, Y. Conversion of Chemical Into Mechanical Energy by Synthetic Polymers (Chemomechanical Systems). Vol. 82, pp. 1—47. [Pg.158]

Researchers are facing difficulties in improving the properties and response rates of chemomechanical andelectrochemomechanical systems based on polymer gels or proteins that are intended to be used as actuators in robotics. Lack of mechanical toughness and long-term durability are other problems to be solved. A basic improvement in the low efficiency... [Pg.360]

Microtubule-associated proteins bind to microtubules in vivo and subserve a number of functions including the promotion of microtubule assembly and bundling, chemomechanical force generation, and the attachment of microtubules to transport vesicles and organelles (Olmsted, 1986). Tubulin purified from brain tissue by repeated polymerization-depolymerization contains up to 20% MAPs. The latter can be dissociated from tubulin by ion-exchange chromatography. The MAPs from brain can be resolved by sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE). [Pg.6]

Dynein, kinesin, and myosin are motor proteins with ATPase activity that convert the chemical bond energy released by ATP hydrolysis into mechanical work. Each motor molecule reacts cyclically with a polymerized cytoskeletal filament in this chemomechanical transduction process. The motor protein first binds to the filament and then undergoes a conformational change that produces an increment of movement, known as the power stroke. The motor protein then releases its hold on the filament before reattaching at a new site to begin another cycle. Events in the mechanical cycle are believed to depend on intermediate steps in the ATPase cycle. Cytoplasmic dynein and kinesin walk (albeit in opposite... [Pg.16]

Even though dynein, kinesin, and myosin serve similar ATPase-dependent chemomechanical functions and have structural similarities, they do not appear to be related to each other in molecular terms. Their similarity lies in the overall shape of the molecule, which is composed of a pair of globular heads that bind microtubules and a fan-shaped tail piece (not present in myosin) that is suspected to carry the attachment site for membranous vesicles and other cytoplasmic components transported by MT. The cytoplasmic and axonemal dyneins are similar in structure (Hirokawa et al., 1989 Holzbaur and Vallee, 1994). Current studies on mutant phenotypes are likely to lead to a better understanding of the cellular roles of molecular motor proteins and their mechanisms of action (Endow and Titus, 1992). [Pg.17]

The contractile apparatus may be thought of as the sum of those intracellular components which constitute the machinery of chemomechanical transduction. It is the set of proteins which convert the chemical energy of the terminal phosphate ester bond of ATP into mechanical work. The structure of the contractile apparatus is determined by the connections between the various protein molecules via specific binding sites or, in a minority of cases, via labile covalent linkages. The kinetics of the contractile machinery are determined by the regulation of changes in these connections. [Pg.169]

Although the fundamental chemomechanical transduction processes seem to be the same in all types of vertebrate muscle, contraction in smooth muscle is characterized by much greater involvement of enzymatically catalyzed control reactions. In smooth muscle the control reactions themselves involve the use of phosphorylation-dephosphorylation cycles. Moreover, they are futile in the sense they cause the expenditure of bond energy without a tangible work resultant, i.e., compounds synthesized or external work done. [Pg.171]

For the purpose of discussion, crossbridge regulation can be split into three overlapping sets of reactions (a) the Ca-calmodulin cascade (MLCK activation), (b) the phosphorylation-dephosphorylation cycle (the Four State Model), and (c) actin-myosin cycle (chemomechanical transduction). [Pg.178]

The mechanical behavior of the contractile apparatus of smooth muscle is also very similar to that of striated muscle. So that to the extent that the force-velocity curves reflect the interaction of mechanical force and the rate of enzymatic catalysis, the steps of the chemomechanical transduction cycles in the two muscles are apparently modulated in similar ways. Also relationships between the active isometric force and muscle length are very similar (except as noted above for shorter lengths). [Pg.183]

Larsen-Basse, J. and Liang, H., Probable Role of Abrasion in Chemomechanical Polishing of Tungsten," Wear, Vol. 233-... [Pg.267]

Y Osada. Conversion of chemical into mechanical energy by synthetic polymers (chemomechanical systems). Adv Polym Sci 81 1-46, 1987. [Pg.585]

CMOS complementary metal oxide semiconductor CMP chemomechanical polishing... [Pg.245]

Brazel, C. S. and Peppas, N. A. Synthesis and characterization of thermo- and chemomechanically responsive poly(A-isopropylacrylamide-co-methacryhc acid) hydrogels. Macromolecules 1995, 28, 8016-8020. [Pg.173]

Reports of building up two-dimensional polymers have been published by several research groups [9-12]. Additional reports [13-15] and a review [16] have appeared on stimuli-responsive polymer gels and their application to chemomechanical systems. The preparation and application of new monosized polymer particles have been reviewed [17]. [Pg.210]

Linford and coworkers have shown that the attachment of alkenes to H-terminated silicon surfaces can also be initiated by direct mechanical scribing, in a process termed chemomechanical functionalization [145-147]. The reaction of 1-alkenes (as well as 1-alkynes) leads to attachment of the molecule to the surface through two new Si—C bonds. The proposed mechanism is the mechanical cleavage of Si—H and Si—Si bonds, leading to silicon radicals that then react with the reactive liquid. Interestingly, Linford and coworkers have also extended this work to show that chemomechanical functionalization can be carried out not only on H-terminated Si, but also on sihcon covered with oxide, and have shown that the process works with a variety of halides, alcohols, and epoxides in both the liquid and gas phase [146]. [Pg.343]

Wacaser, B. A., Maughan, M. J., Mowat, I. A., Niederhauser, T. L., Linford, M. R. and Davis, R. C. Chemomechanical surface patterning and functionalization of silicon surfaces using an atomic force microscope. Applied Physics Letters 82, 808 (2003). [Pg.386]

There are several mechanisms which are essentially different in chemomechanical reactions of polymer molecular level structure changes, polymer conformational change, change of polymer-polymer interactions and the change of crosslinked structure in polymer gels. [Pg.243]


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CHEMOMECHANICAL ACTUATORS AND SENSORS

Chemomechanical Systems Based on Redox Reactions

Chemomechanical Systems Based on Steric Photo-Isomerization

Chemomechanical devices

Chemomechanical effect

Chemomechanical instabilities

Chemomechanical oscillators

Chemomechanical polishing

Chemomechanical response

Chemomechanical sensors

Chemomechanical system

Chemomechanical transduction

Chemomechanical transduction efficiencies

Coupling chemomechanical

Efficiency chemomechanical

Energy conversion, chemomechanical

Glucose-driven chemomechanical

Glucose-driven chemomechanical oscillator

Mechanisms of Chemomechanical Reactions

Spatial Bistability and Related Chemomechanical Instabilities

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