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Updated: Feb 14, 2026

Measuring Protein Binding to F-actin by Co-sedimentation
Published on: May 18, 2017
Measurement of Average Aggregate Density by Sedimentation and Brownian Motion Analysis
Richard E Cavicchi1, Jason King2, Dean C Ripple1
1Bioprocess Measurements Group, National Institute of Standards and Technology, Gaithersburg, Maryland 20899.
None:
The spatially averaged density of protein aggregates is an important parameter that can be used to relate size distributions measured by orthogonal methods, to characterize protein particles, and perhaps to estimate the amount of protein in aggregate form in a sample. We obtained a series of images of protein aggregates exhibiting Brownian diffusion while settling under the influence of gravity in a sealed capillary. The aggregates were formed by stir-stressing a monoclonal antibody (NISTmAb). Image processing yielded particle tracks, which were then examined to determine settling velocity and hydrodynamic diameter down to 1 microm based on mean square displacement analysis. Measurements on polystyrene calibration microspheres ranging in size from 1 to 5 microm showed that the mean square displacement diameter had improved accuracy over the diameter derived from imaged particle area, suggesting a future method for correcting size distributions based on imaging. Stokes' law was used to estimate the density of each particle. It was found that the aggregates were highly porous with density decreasing from 1.080 to 1.028 g/cm3 as the size increased from 1.37 to 4.9 microm.
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