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Method Article

In Vitro Polymerization of F-actin on Early Endosomes

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DOI:

10.3791/55829

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August 28th, 2017

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In This Article

Summary

Early endosome functions depend on F-actin polymerization. Here, we describe a microscopy-based in vitro assay that reconstitutes the nucleation and polymerization of F-actin on early endosomal membranes in test tubes, thus rendering this complex series of reactions amenable to biochemical and genetic manipulations.

Abstract

Many early endosome functions, particularly cargo protein sorting and membrane deformation, depend on patches of short F-actin filaments nucleated onto the endosomal membrane. We have established a microscopy-based in vitro assay that reconstitutes the nucleation and polymerization of F-actin on early endosomal membranes in test tubes, thus rendering this complex series of reactions amenable to genetic and biochemical manipulations. Endosomal fractions are prepared by floatation in sucrose gradients from cells expressing the early endosomal protein GFP-RAB5. Cytosolic fractions are prepared from separate batches of cells. Both endosomal and cytosolic fractions can be stored frozen in liquid nitrogen, if needed. In the assay, the endosomal and cytosolic fractions are mixed, and the mixture is incubated at 37 °C under appropriate conditions (e.g., ionic strength, reducing environment). At the desired time, the reaction mixture is fixed, and the F-actin is revealed with phalloidin. Actin nucleation and polymerization are then analyzed by fluorescence microscopy. Here, we report that this assay can be used to investigate the role of factors that are involved either in actin nucleation on the membrane, or in the subsequent elongation, branching, or crosslinking of F-actin filaments.

Introduction

In higher eukaryotic cells, proteins and lipids are internalized into early endosomes where sorting occurs. Some proteins and lipids, which are destined to be reutilized, are incorporated into tubular regions of the early endosomes and then transported to the plasma membrane or to the trans-Golgi network (TGN)1,2. By contrast, other proteins and lipids are selectively packaged into regions of the early endosomes that exhibit a multivesicular appearance. These regions expand and, upon detachment from early endosomal membranes, eventually mature into free endosomal carrier vesicles or multivesicular bodies (ECV/....

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Protocol

1. Solutions and Preparations

NOTE: All buffers and solutions should be prepared in double-distilled (dd) H2O. Because the hydration state of sucrose varies, the final concentration of all sucrose solutions must be determined using a refractometer.

  1. Prepare phosphate-buffered saline without divalent cations (PBS-): 137 mM NaCI, 2.7 mM KCl, 1.5 mM KH2PO4, and 6.5 mM Na2HPO4. Adjust the pH to 7.4. Sterilize by autoclaving (1 cycle at 121 °C for 15 min) and store at room temperature.
  2. Prepare stock solution of 300 mM imidazole: 0.204 g of imidazole in 10 mL of ddH<....

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Results

To gain insights into the formation of F-actin patches on early endosome membranes, we followed the protocol outlined in Figure 2. Briefly, cells were transfected with GFP-RAB5 and then early endosomes were prepared by subcellular fractionation. These purified early endosomes were incubated with cytosol in order to provide actin itself as well as other factors possibly involved in the reaction. At the end of the incubation period, the reaction was stopped by .......

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Discussion

Actin plays a crucial role in endosome membrane dynamics4,14. We previously reported that actin nucleation and polymerization occur on early endosomes, forming small F-actin patches or networks. These F-actin networks are absolutely required for membrane transport beyond early endosomes along the degradation pathway. Interfering at any step of this nucleation and polymerization process prevents endosome maturation and thus downstream transport towards late endoso.......

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Disclosures

The authors declare that they have no competing financial interests.

Acknowledgements

Support was received from the Swiss National Science Foundation; the Swiss Sinergia program; the Polish-Swiss Research Programme (PSPB-094/2010); the NCCR in Chemical Biology; and LipidX from the Swiss SystemsX.ch initiative, evaluated by the Swiss National Science Foundation (to J. G.). O. M. was supported by an EMBO long-term fellowship (ALTF-516-2012).

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Materials

List of materials used in this article
NameCompanyCatalog NumberComments
NaClSigma-Aldrich71380
KClAcros Organics196770010
KH2PO4AppliChemA1042
Na2HPO4Acros Organics424370025
HepesAppliChemA3724
Magnesiun acetate tetrahydrateFluka63047
Dithiothreitol (DTT)AppliChemA2948
ImidazoleSigma-Aldrich10125
NaOHFluka71690
SucroseMerck Millipore107687
LeupeptinRoche11017101001
PepstatinRoche10253286001
AprotininRoche10236624001
ParaformaldehidePolysciences. Inc380
Alexa Fluor 555 phalloidinMolecular ProbesA34055
Actin rhodamineCytoskeleton. IncAPHR-A
Mowiol 4-88Sigma-Aldrich81381poly(vinyl alcohol), Mw ~31 000
DABCOSigma-AldrichD-2522
Tris-HClAppliChemA1086
β-caseinSigma-AldrichC6905
Filter 0.22 μmMillexSL6V033RS
Round 10 cm dishes for cell cultureThermo Fisher Scientific150350
Plastic Pasteur pipetteAssistent569/3 40569003
15-mL polypropylen tubeTPP91015
Hypodermic Needle 22G Black 30mmBD Microlance300900
Sterile Luer-slip 1mL Syringes without needleBD Plastipak300013
Micro glass slidesAssistent2406
18 x 18-mm glass coverslipAssistent1000/1818
SW60 centrifuge tubeBeckman coulter344062
TLS-55 centrifuge tubeBeckman coulter343778
200-μL yellow tipStarlabS1111-0706
1,000-μL Blue Graduated TipStarlabS1111-6801
1.5-mL test tubeAxygenMCT-175-C 311-04-051
18-mm diameter round coverslipAssistent1001/18
35-mm diameter round dish with a 20-mm glass bottom (0.16 - 0.19 mm)In vitro ScientificD35-20-1.5-N
RefractometerCarl Zeiss79729
Plasma cleanerHarrick PlasmaPDC-32G
Sorvall WX80 UltracentrifugeThermo Fisher Scientific46900
Tabletop ultracentrifugeBeckman coulterTL-100
SW60 rotorBeckman coulter335649
TLS-55 rotorBeckman coulter346936
Confocal microscopyCarl ZeissLSM-780
Fugene HD transfection reagentPromegaE2311
Protein assay reagent ABio-Rad500-0113
Protein assay reagent BBio-Rad500-0114
Protein assay reagent SBio-Rad500-0115
Cell scraperHomemadeSilicone rubber piece of about 2 cm, cut at a very sharp angle and attached to a metal bar or held with forceps
RefractometerCarl Zeiss
Minimum Essential Medium Eagle (MEM)Sigma-AldrichM0643
FCSThermo Fisher Scientific10270-106
MEM Non-Essential Amino Acids (NEAA)Thermo Fisher Scientific11140-035
L-GlutamineThermo Fisher Scientific25030-024
Penicillin-StreptomycinThermo Fisher Scientific15140-122
pH Meter 691Metrohm
ImageJ softwareNIH, Bethesda MD

References

  1. Huotari, J., Helenius, A. Endosome maturation. EMBO J. 30 (17), 3481-3500 (2011).
  2. Scott, C. C., Vacca, F., Gruenberg, J. Endosome Maturation, Transport and Functions. Semin. Cell Dev Biol. 31, 2-10 (2014).
  3. Puthenveedu, M. A., et al.

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