A subscription to JoVE is required to view this content. Sign in or start your free trial.

Method Article

TIRF Microscopy to Visualize Actin and Microtubule Coupling Dynamics

2.5K views

⸱

July 8th, 2025

In This Article

Abstract

Source: Henty-Ridilla, J.L., Visualizing Actin and Microtubule Coupling Dynamics In Vitro by Total Internal Reflection Fluorescence (TIRF) Microscopy. J. Vis. Exp. (2022)

This video describes TIRF, a total internal reflection microscopy-based technique to visualize actin and microtubule polymerization dynamics. The method allows the high-resolution imaging of actin and microtubule coupling dynamics in real-time, which is essential for understanding cellular crosstalks.

Protocol

1. Washing the coverslips

NOTE: Wash (24 mm x 60 mm, #1.5) coverslips according to Smith et al., 2013.

  1. Arrange coverslips in a plastic slide mailer container.
  2. Submerge coverslips sequentially in the following solutions and sonicate for 30-60 min, rinsing with ddH2O 10 times in between each solution: ddH2O with one drop of dish soap; 0.1 M KOH. Store coverslips in 100% ethanol for up to 6 months.
    NOTE: Do not touch glass surfaces with ungloved fingers. Use forceps instead.

2. Coating cleaned ....

Access restricted. Please log in or start a trial to view this content.

Results

TIRF microscopy imaging setup showing assembly, illumination process, and sample composition details.
Figure 1. Experimental schematics: flow chamber assembly to image acquisition. (A) Imaging chamber assembly. Top to bottom: IBIDI imaging chambers are taped along perfusion wells (denoted by arrow); the second (white) layer of tape backing (left on in the image shown .......

Access restricted. Please log in or start a trial to view this content.

Disclosures

No conflicts of interest declared.

Materials

List of materials used in this article
NameCompanyCatalog NumberComments
1% BSA (w/v)Fisher ScientificBP1600-100For this purpose (blocking TIRF chambers), BSA is resuspended in ddH20 and filtered through a 0.22 µm filter.
1× BRB80Homemade80 mM PIPES, 1 mM MgCl2, 1 mM EGTA, pH 6.8 with KOH
80 mM PIPES, 1 mM MgCl2, 1 mM EGTA, pH 6.8 with KOHSigma Aldrich Inc, St. Louis, MOG2133-50KUCombined with catalase, aliquot and store at -80 oC until use
100 µM tubulinCytoskeleton Inc, Denver, COT240Homemade tubulins should be recycled before use to remove polymerization-incompetent tubulin (Hyman et al. (1992)29; Li and Moore (2020)30 ). Commercially available tubulins are often too dilute to recycle but function well if resuspended according to the manufacturer’s instructions and pre-cleared via ultracentrifugation (278,000 × g) for 60 min, before use.
100 mM ATPGold Biotechnology Inc, Olivette, MOA-08Resuspended in ddH20 (pH 7.5) and filter sterilized.
100 mM GTPFisher ScientificAC226250010Resuspended in 1× BRB80 (pH 6.8) and filter sterilized.
120-150 mW solid-state lasersLeica Microsystems11889151; 11889148
2 mg/mL catalaseSigma Aldrich Inc, St. Louis, MOC40-100Combined with glucose oxidase, aliquot and store at -80 oC until use
2× TIRF bufferHomemad2× BRB80, 100 mM KCl, 20 mM DTT, 80 mM glucose, 0.5% (v/v) methylcellulose (4,000 cp); Note: 1 µL of 0.1M GTP and 1 µL of 0.1M ATP added separately to TIRF reactions to avoid repeated freeze-thaw cycles.
24 × 60 mm, #1.5 coverglassFisher Scientific, Waltham, MA22-266882Coverglass must be extensively washed before use (Smith et al. (2014)22 )
37 oC heatblock
37 oC water bath
5 mg/mL Streptavidin (600x stock)Avantor, Philadelphia, PARLS000-01Resuspended in Tris-HCl (pH 8.8); dilute the aliquot to 1× in HEK buffer on day of use
5 min Epoxy resin and hardenerLoctite, Rocky Hill, CT1365736Combined resin and hardener may take up to 30 min to cure.
50% biotinylated-GpCpp microtubule seedsCytoskeleton Inc; HomemadeT333P(optional) GppCpp or Taxol stabilized microtubule seeds can more efficiently mediate microtubule polymerization. Taxol and GppCpp stabilize microtubules in different ways that can affect the microtubule lattice structure and the ability of certain regulatory proteins to bind to the stabilized portion of the microtubule. A method to make diverse kinds of microtubule seeds is outlined in Hyman et al. (1992).
70 C incubator
Actin mix stockHomemade; this protocolA 12.5 µM actin mix comprised of labeled (fluorescent and biotinylated) and unlabeled actin for up to six reactions. 2 µL of stock is used in the final TIRF reaction. The final concentration of actin used in each reaction is 0.5 µM (10% Alexa-647; 0.09% biotin-labeled).
Appropriate buffer controlsHomemadeCombination of buffers from all proteins being assessed
Biotin-PEG-silane (MW 3,400)Laysan Bio Incbiotin-PEG-SIL-3400Dispensed into 2-5 mg aliquots, backfilled with nitrogen, parafilmed closed, and stored at -20 C with desiccant until use
Biotinylated actinCytoskeleton Inc; HomemadeAB07Biotin-actin is made by labeling on lysine residues and thus assumed to be at least 100% labeled, but varies with different lots/preparations. Optimal biotinylated actin concentrations must be empirically determined for particular uses/experimental designs. Higher concentrations permit more efficient tracking, but may impede polymerization or interactions with regulatory proteins. Here, a small percentage (0.09% or 900 pM) biotinylated actin is present in the final TIRF reaction.
Dish soapDawn, Procter and Gamble, Cincinnati, OHFor unknown reasons, the blue version cleans coverslips more efficiently than other available colors.
Dry ice
Fluorescently labeled actinCytoskeleton Inc; HomemadeAR05Homemade fluorescently labeled-actin is stored in G-buffer supplemented with 50% glycerol at -20 C (Spudich et al. (1971) 47; Liu et al. (2022)48 ). Fluorescently-labeled actin is dialyzed against G-buffer and precleared via ultracentrifugation for 60 min at 278,000 × g before use.
Fluorescently labeled tubulinCytoskeleton IncTL488M, TLA590M, TL670MResuspended in 20 µL 1× BRB80 (10 µM final concentration) and pre-cleared via ultracentrifugation (278,000 × g) for 60 min, before use.
G-bufferHomemade3 mM Tris-HCl (pH 8.0), 0.2 mM CaCl2, 0.5 mM DTT, 0.2 mM ATP
HEK BufferHomemade20 mM HEPES (pH 7.5), 1 mM EDTA (pH 8.0), 50 mM KCl
Ice
Ice bucket
Imaging chamberIBIDI, Fitchburg, WI80666Order chambers with no bottom to utilize different coverslip coatings
iXon Life 897 EMCCD cameraAndor, Belfast, Northern Ireland8114137
LASX Premium microscope softwareLeica Microsystems8114137
Methylcellulose (4,000 cp)Sigma Aldrich IncM0512
Microscope base equipped with TIRF moduleLeica Microsystems, Wetzlar, Germany11889146
mPEG-silane (MW 2,000)

Explore More Articles

Actin Microtubule CouplingCytoskeleton DynamicsFluorescence ImagingPolymerization DynamicsFlow Chamber AssemblyFluorophore LabelingProtein Reaction MixPerfusion Chamber SetupTime-lapse Imaging