Method Article

Interference Reflection Microscopy for Label-Free Visualization of Microtubule Dynamics

July 8th, 2025

In This Article

Abstract

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Source: Mahamdeh, M., et al. Implementation of Interference Reflection Microscopy for Label-free, High-speed Imaging of Microtubules. J. Vis. Exp. (2019).

In this video, we describe the interference reflection microscopy (IRM) technique to visualize microtubules growing on a coverslip surface in the presence of a suitable buffer. Upon illumination with incident light, the coverslip-buffer interface and buffer-microtubule interface reflect light, which combines to create an interference pattern, enabling the visualization of microtubules as high-contrast images against a bright background.

Protocol

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1. Microscope modification and objective lens

  1. Insert a 50/50 mirror into the filter wheel of the fluorescent microscope using an appropriate filter cube (Figure 1). Handle the 50/50 mirror with care as often they have anti-reflection coating.
    NOTE: We used a 50/50 mirror in an empty filter cube of the microscope. The 50/50 mirror is inserted where the dichroic mirror is located.
  2. Use a high magnification/high numerical aperture (NA) oil objective.
    NOTE: In this protocol, we used a 100x/1.3 NA objective.

2. Chamber preparation ....

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Results

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Microtubule growth microscope setup, optical path diagram, assembly process for imaging experiment.
Figure 1. Schematic representation of IRM. (A) Epi-illumination from the light source passes through the aperture diaphragm before reaching the 50/50 mirror. The aperture diaphragm sets the beam width thus the illumination NA. The 50/50 mirror partially reflects the light up to the obje.......

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Disclosures

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No conflicts of interest declared.

Materials

List of materials used in this article
NameCompanyCatalog NumberComments
MicroscopeNikonTi-EclipseAn inverted microscope used for perfoming the expriments
50/50 beam splitterChroma21000When buying make sure to choose the splitter dimensions that fit the cube used in the microscope
NIKON PLAN FLUOR 100X/0.5-1.3 Iris objectiveNikonMRH02902Imaging objective. This objective has a NA adjusting iris that was opened to NA 1.3
Mucasol universal detergentSigma-AldrichZ637181-2LUsed for cleaning coverslips and slides
Plastic paraffin film (commerical name Parafilm M)Sigma-AldrichP7793Used for constructing flow channels
Anti-TAMRA antibodyInvitrogenA-6397Used to bind TAMRA-labeled molecules (e.g. microtubules) to the sample surface. RRID (AB_2536196)
Poloxamer 407 (commercial name Pluronic F-127)Sigma-AldrichUsed for blocking the channel surface to prevent nonspecific binding
40 nm gold nanoparticlesSigma-Aldrich753637Used as a control sample
20 nm gold nanoparticlesSigma-Aldrich753610Used as a control sample
Zyla 4.2 CameraAndorZyla 4.22048x2048 pixles (6.5µm pixel size) with quantum efficiency of 72% and 16bit dynamic range
Feista tracking softwarehttps://www.bcube-dresden.de/ fiesta/wiki/FIESTA
Stabilized microtubulesPrepared in house (see references in text)

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Tags

Interference Reflection MicroscopyMicrotubule DynamicsLabel Free ImagingMicrotubule GrowthMicrotubule ShrinkageAntibody CoatingParaffin ChannelTime Lapse ImagingAperture DiaphragmBRB80 Buffer

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