| Torque-Speed Relationship of the Flagellar Rotary Motor of Escherichia coli Biophysical Journal, Volume 78, Issue 2, 1 February 2000, Pages 1036-1041 Xiaobing Chen and Howard C. Berg Abstract The output of a rotary motor is characterized by its torque and speed. We measured the torque-speed relationship of the flagellar rotary motor of by a new method. Small latex spheres were attached to flagellar stubs on cells fixed to the surface of a glass slide. The angular speeds of the spheres were monitored in a weak optical trap by back-focal-plane interferometry in solutions containing different concentrations of the viscous agent Ficoll. Plots of relative torque (viscosity×speed) versus speed were obtained over a wide dynamic range (up to speeds of ∼300Hz) at three different temperatures, 22.7, 17.7, and 15.8°C. Results obtained earlier by electrorotation (Berg and Turner, 1993, 65:2201–2216) were confirmed. The motor operates in two dynamic regimes. At 23°C, the torque is approximately constant up to a knee speed of nearly 200Hz, and then it falls rapidly with speed to a zero-torque speed of ∼350Hz. In the low-speed regime, torque is insensitive to changes in temperature. In the high-speed regime, it decreases markedly at lower temperature. These results are consistent with models in which torque is generated by a powerstroke mechanism (Berry and Berg, 1999, 76:580–587). Abstract | Full Text | PDF (135 kb) |
| The Hydrodynamic Radii of Macromolecules and Their Effect on Red Blood Cell Aggregation Biophysical Journal, Volume 87, Issue 6, 1 December 2004, Pages 4259-4270 J.K. Armstrong, R.B. Wenby, H.J. Meiselman and T.C. Fisher Abstract The effects of nonionic polymers on human red blood cell (RBC) aggregation were investigated. The hydrodynamic radius () of individual samples of dextran, polyvinylpyrrolidone, and polyoxyethylene over a range of molecular weights (1500–2,000,000) were calculated from their intrinsic viscosities using the Einstein viscosity relation and directly measured by quasi-elastic light scattering, and the effect of each polymer sample on RBC aggregation was studied by nephelometry and low-shear viscometry. For all three polymers, despite their different structures, samples with <4nm were found to inhibit aggregation, whereas those with >4nm enhanced aggregation. Inhibition increased with and was maximal at ∼3nm; above 4nm the pro-aggregant effect increased with . For comparison, the of 12 plasma proteins were calculated from literature values of intrinsic viscosity or diffusion coefficient. Each protein known to promote RBC aggregation had >4nm, whereas those with <4nm either inhibited or had no effect on aggregation. These results suggest that the influence of a nonionic polymer or plasma protein on RBC aggregation is simply a consequence of its size in an aqueous environment, and that the specific type of macromolecule is of minor importance. Abstract | Full Text | PDF (216 kb) |
| Visualizing Ion Relaxation in the Transport of Short DNA Fragments Biophysical Journal, Volume 76, Issue 5, 1 May 1999, Pages 2488-2501 Stuart A. Allison, Hua Wang, Thomas M. Laue, Timothy J. Wilson and John O. Wooll Abstract Ion relaxation plays an important role in a wide range of phenomena involving the transport of charged biomolecules. Ion relaxation is responsible for reducing sedimentation and diffusion constants, reducing electrophoretic mobilities, increasing intrinsic viscosities, and, for biomolecules that lack a permanent electric dipole moment, provides a mechanism for orienting them in an external electric field. Recently, a numerical boundary element method was developed to solve the coupled Navier-Stokes, Poisson, and ion transport equations for a polyion modeled as a rigid body of arbitrary size, shape, and charge distribution. This method has subsequently been used to compute the electrophoretic mobilities and intrinsic viscosities of a number of model proteins and DNA fragments. The primary purpose of the present work is to examine the effect of ion relaxation on the ion density and fluid velocity fields around short DNA fragments (20 and 40 bp). Contour density as well as vector field diagrams of the various scalar and vector fields are presented and discussed at monovalent salt concentrations of 0.03 and 0.11M. In addition, the net charge current fluxes in the vicinity of the DNA fragments at low and high salt concentrations are briefly examined and discussed. Abstract | Full Text | PDF (1174 kb) |
Copyright © 1964 The Biophysical Society. All rights reserved.
Biophysical Journal, Volume 4, Issue 1, 11-21, 1 January 1964
doi:10.1016/S0006-3495(64)86766-7
Articles
N.L. Incardona and Paul Kaesberg
Bromegrass mosaic virus undergoes a reversible decrease in its sedimentation coefficient when the pH is raised above pH 6.7. At pH 6 the sedimentation coefficient is 87 S, at pH 7 it is 79 S. Intrinsic viscosities determined at pH 6 and 7 are 3.64 and 5.5×10-2 dl/gm. Diffusion coefficients are 1.56×10-7 cm2/sec. and 1.44×10-7 cm2/sec., respectively. Radii of gyration, measured by x-ray scattering, are 106 and 128 A. However, appropriate combination of sedimentation, diffusion, and viscosity coefficients at pH 6 and 7 yield the same molecular weight. Also, the zero-angle value of x-ray-scattered intensity, which is a function of molecular weight, is the same at the two pH's. These results suggest that bromegrass mosaic virus particles undergo a pH-induced change in structure. This change causes, among other things, an increase in the susceptibility of the particles to degradation by pancreatic ribonuclease. The shape of the titration curve between pH 6.3 and 6.9 is anomalous.