Actin filament mechanics in the laser trap

Numerous biological processes, including muscular contraction, depend upon the mechanical properties of actin filaments. One such property is resistance to bending (flexural rigidity, EI). To estimate EI, we attached the ends of fluorescently labelled actin filaments to two microsphere‘handles’ captured in independent laser traps. The positions of the traps were manipulated to apply a range of tensions (0--8 pN)to the filaments via the microsphere handles. With increasing filament tension, the displacement of the microspheres was inconsistent with a microsphere-filament system that is rigid. We maintain that this inconsistency is due to the microspheres rotating in the trap and the filaments bending near their attachments to accommodate this rotation. Fitting the experimental data to a simple model of this phenomena, we estimate actin's EI to be ×15 × 103 pN nm2, a value within the range of previously reported results, albeit using a novel method. These results both: support the idea that actin filaments are more compliant than historically assumed; and, indicate that without appropriately pretensioning the actin filament in similar laser traps, measurements of unitary molecular events (e.g. myosin displacement) may be significantly underestimated

[1]  K. Trybus,et al.  Smooth muscle myosin cross-bridge interactions modulate actin filament sliding velocity in vitro , 1990, The Journal of cell biology.

[2]  Christoph F. Schmidt,et al.  Direct observation of kinesin stepping by optical trapping interferometry , 1993, Nature.

[3]  T. Yanagida,et al.  Compliance of thin filaments in skinned fibers of rabbit skeletal muscle. , 1995, Biophysical journal.

[4]  K. Svoboda,et al.  Biological applications of optical forces. , 1994, Annual review of biophysics and biomolecular structure.

[5]  Smooth Muscle Myosin , 1998 .

[6]  S. Block One small step for myosin... , 1995, Nature.

[7]  A. Mehta,et al.  Characterization of single actin-myosin interactions. , 1995, Biophysical journal.

[8]  F. Oosawa Actin-actin bond strength and the conformational change of F-actin. , 1977, Biorheology.

[9]  Toshio Yanagida,et al.  Direct observation of motion of single F-actin filaments in the presence of myosin , 1984, Nature.

[10]  Edward H. Egelman,et al.  The structure of F-actin , 1985, Journal of Muscle Research & Cell Motility.

[11]  J. Spudich,et al.  Purification of muscle actin. , 1982, Methods in cell biology.

[12]  Toshio Yanagida,et al.  Force measurements by micromanipulation of a single actin filament by glass needles , 1988, Nature.

[13]  A. Ashkin Forces of a single-beam gradient laser trap on a dielectric sphere in the ray optics regime. , 1992, Methods in cell biology.

[14]  S. Lowey,et al.  Preparation of myosin and its subfragments from rabbit skeletal muscle. , 1982, Methods in enzymology.

[15]  U. Aebi,et al.  The structure of the F-actin filament and the actin molecule. , 1992, Current opinion in cell biology.

[16]  S. Chu,et al.  Laser Manipulation of Atoms and Particles , 1991, Science.

[17]  S. Ishiwata,et al.  Stepwise motion of an actin filament over a small number of heavy meromyosin molecules is revealed in an in vitro motility assay. , 1994, Journal of biochemistry.

[18]  A. Huxley,et al.  The relation between stiffness and filament overlap in stimulated frog muscle fibres. , 1981, The Journal of physiology.

[19]  Y Ueno,et al.  X-ray diffraction evidence for the extensibility of actin and myosin filaments during muscle contraction. , 1994, Biophysical journal.

[20]  H E Huxley,et al.  X-ray diffraction measurements of the extensibility of actin and myosin filaments in contracting muscle. , 1994, Biophysical journal.

[21]  H. Isambert,et al.  Flexibility of actin filaments derived from thermal fluctuations. Effect of bound nucleotide, phalloidin, and muscle regulatory proteins , 1995, The Journal of Biological Chemistry.

[22]  R. T. Tregear,et al.  Movement and force produced by a single myosin head , 1995, Nature.

[23]  S. Asakura,et al.  Dark-field light microscopic study of the flexibility of F-actin complexes. , 1980, Journal of molecular biology.

[24]  J. Käs,et al.  Direct Measurement of the Wave-Vector-Dependent Bending Stiffness of Freely Flickering Actin Filaments , 1993 .

[25]  S. Lowey,et al.  [7] Preparation of myosin and its subfragments from rabbit skeletal muscle , 1982 .

[26]  W. Kabsch,et al.  Structure and function of actin. , 1992, Annual review of biophysics and biomolecular structure.

[27]  A. Huxley,et al.  Actin compliance: are you pulling my chain? , 1994, Biophysical journal.

[28]  Kazuhiko Kinosita,et al.  Unbinding force of a single motor molecule of muscle measured using optical tweezers , 1995, Nature.

[29]  Steven M. Block,et al.  Transcription Against an Applied Force , 1995, Science.

[30]  D. Warshaw,et al.  Enhanced force generation by smooth muscle myosin in vitro. , 1994, Proceedings of the National Academy of Sciences of the United States of America.

[31]  J. Spudich,et al.  Single myosin molecule mechanics: piconewton forces and nanometre steps , 1994, Nature.

[32]  J. Howard,et al.  Flexural rigidity of microtubules and actin filaments measured from thermal fluctuations in shape , 1993, The Journal of cell biology.

[33]  J. Hearst,et al.  On Polymer Dynamics , 1966 .

[34]  T. Yanagida,et al.  Direct measurement of stiffness of single actin filaments with and without tropomyosin by in vitro nanomanipulation. , 1994, Proceedings of the National Academy of Sciences of the United States of America.