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Table · dataset · 2025

Supporting Information for TIRF microscopy evanescent field calibration using tilted fluorescent microtubules.

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Total internal reflection fluorescence microscopy has become a powerful tool to study the dynamics of sub-cellular structures and single molecules near substrate surfaces.

Description

However, the penetration depth of the evanescent field, that is, the distance at which the excitation intensity has exponentially decayed to 1/e, is often left undetermined. This presents a limit on the spatial information about the imaged structures.

Here, we present a novel method to quantitatively characterize the illumination in total internal reflection fluorescence microscopy using tilted, fluorescently labelled, microtubules. We find that the evanescent field is well described by a single exponential function, with a penetration depth close to theoretically predicted values. The use of in vitro reconstituted microtubules as nanoscale probes results in a minimal perturbation of the evanescent field; excitation light scattering is eliminated and the refractive index of the sample environment is unchanged.

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The presented method has the potential to provide a generic tool for in situ calibration of the evanescent field.

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Condensed matter physics 69% · Microscopy 75%
Provenance · 2 source records, 21 field assertions
SourceKeyLast seenRaw
Edmonddoi:10.17617/3.GMINAX12 d agoJSON v1
Edmonddoi:10.17617/3.GMINAX11 d agoJSON v1
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