Abstract
Traction force microscopy (TFM) is a powerful approach of quantifying cell-material interactions, which over the last two decades has contributed significantly to our understanding of cellular mechanosensing and mechanotransduction. In addition, recent advances in three-dimensional (3D) imaging and traction force analysis (3D TFM) have highlighted the significance of the third dimension in influencing various cellular processes. Yet irrespective of dimensionality almost all TFM approaches have relied on a linear elastic theory framework to calculate cell surface tractions.This talk presents a new high-resolution 3D TFM algorithm, which utilizes a large deformation formulation to quantify cellular displacement fields with unprecedented resolution. The results feature some of the first experimental evidence that cells are indeed capable of exerting large material deformations, which require the formulation of a new theoretical TFM framework to accurately calculate traction forces. Based on our previous 3D TFM technique we reformulate our approach to accurately account for large material deformation and quantitatively contrast and compare both linear and large deformation frameworks as a function of the applied cell deformation. Particular attention is paid in estimating the accuracy penalty associated with utilizing a traditional linear elastic approach in the presence of large deformation gradients.
Highlights
2490-Plat Photobleaching Correction in Fluorescence Correlation Spectroscopy Rudra P
Fluorescence correlation spectroscopy (FCS) is a fluorescence technique conventionally used to study the kinetics of fluorescent molecules in a dilute solution
As a result, photobleaching becomes a problem: the number of photons available to calculate the intensity autocorrelation function is limited, and the decay of the fluorescence intensity itself contributes a spurious signal to the autocorrelation function that can obscure the signature of the molecular dynamics of interest
Summary
2490-Plat Photobleaching Correction in Fluorescence Correlation Spectroscopy Rudra P. The intensity ratio of fluorescence emission at 410nm and 550nm may be useful to monitor the levels of NADþ /NADPþ in aqueous solutions, cellular extracts and living cells. 2489-Plat Non-Destructive Label-Free Monitoring of Drug Intake in Live Cells using ATR FT-IR Spectroscopy Pedro L.
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