Method Article

In situ TEM of Biological Assemblies in Liquid

DOI:

10.3791/50936

āø±

December 30th, 2013

In This Article

Erratum Notice

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Erratum

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Formal Correction: Erratum: In situ TEM of Biological Assemblies in Liquid
Posted by JoVE Editors on 10/10/2024. Citeable Link.

This corrects the article 10.3791/50936

Summary

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Here we describe a procedure to image viral complexes in liquid at nanometer resolution using a transmission electron microscope.

Abstract

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Researchers regularly use Transmission Electron Microscopes (TEMs) to examine biological entities and to assess new materials. Here, we describe an additional application for these instruments- viewing viral assemblies in a liquid environment. This exciting and novel method of visualizing biological structures utilizes a recently developed microfluidic-based specimen holder. Our video article demonstrates how to assemble and use a microfluidic holder to image liquid specimens within a TEM. In particular, we use simian rotavirus double-layered particles (DLPs) as our model system. We also describe steps to coat the surface of the liquid chamber with affinity biofilms that tether DLPs to the viewing window. This permits us to image assemblies in a manner that is suitable for 3D structure determination. Thus, we present a first glimpse of subviral particles in a native liquid environment.

Introduction

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A common goal of biologists and engineers is to understand the inner-workings of molecular machines. Transmission Electron Microscopes (TEMs) are ideal instruments to visualize these intricate details at near-atomic resolution1-2. In order to sustain the high vacuum system of a TEM, biological samples are typically embedded in thin films of vitreous ice3, sugars4, heavy metal salts5, or some combination thereof6. As a result, images of embedded specimens may reveal only limited snapshots of dynamic processes.

Early attempts to maintain biological specimens hydrated in environmental liqu....

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Protocol

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1. Prepare Affinity Capture Devices16

  1. Clean the silicon nitride E-chips by incubating them in 15Ā ml of acetone for 2 min followed by 15Ā ml of methanolĀ for 2 min (FigureĀ 1A). Allow chips to dry under laminar air-flow.
  2. Incubate the dried chips on a heated stir plate (without stirring) for 1.5 hr at 150 °C, then allow them to cool to room temperature before use.
  3. Use Hamilton syringes to compose lipid mixtures in small glass tubes to contain 25% chloroform, 55% DLPC (1,2-dilauroyl-phosphocholine) in chloroform (1 mg/ml) and 20% Ni-NTA lipid (1,2-dioleoyl-....

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Results

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Representative images of DLPs in liquid using E-chips that were glow-discharged (FigureĀ 3A) show fewer DLPs in a given viewing area, presumably due to diffusion, in comparison to DLPs that are enriched on Affinity Capture devices (FigureĀ 3B). The addition of uranyl formate in the imaging chamber enhances the contrast of the specimen and hence the visibility of individual DLPs in solution (FigureĀ 3C, top panel). Better contrast allows for downstream image processing such .......

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Discussion

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In our presented work, we employed the affinity capture approach to tether rotavirus DLPs to a microfluidic platform. This allowed for in situ imaging of macromolecular complexes in a liquid microenvironment. The capture approach is significant with respect to other microfluidic imaging techniques because it localizes biological specimens to the imaging window to negate large diffusive issues that arise while recording images in liquid. However, one of the most critical steps in our protoc.......

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Disclosures

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The author, Madeline J. Dukes, is an employee of Protochips, Inc.

Acknowledgements

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The authors acknowledge Dr. Michael J. Friedlander, Director of the Virginia Tech Carilion Research Institute for encouraging our research endeavors. This project was supported by development funds to S.M.M and D.F.K. and in part by the Nano-Bio initiative of the Institute for Critical Technology and Applied Science at Virginia Tech.

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Materials

List of materials used in this article
NameCompanyCatalog NumberComments
E-chips, spacer chipProtochips, Inc.EPB-52TBD400 μm x 50 μm window
E-chip, top chipProtochips, Inc.EPT-45W400 μm x 50 μm window
Ni-NTA lipidAvanti Polar Lipids790404PPowder form
DLPC (12:0) lipidAvanti Polar Lipids850335PPowder form
Volumetric flasksĀ Fisher Scientific20-812A; 20-812C1 ml; 5 mlĀ 
Hamilton SyringesHamilton Co.80300, 804001-10 μl; 1-25 μl
Whatman #1 filter paperWhatman1001 090100 pieces, 90 mm
Glass Petri dishesCorning70165-101100 mm x 15 mm
Glass Pasteur pipettesVWR14673-01014673-010
Glass culture tubesVWR47729-5666 mm x 50 mm
AcetoneFisher ScientificA11-11 L
MethanolFisher ScientificA412-11 L
ChloroformĀ Electron Microcopy Sciences12550100 mlĀ 
His-tagged Protein AAbcam, Inc.ab5295310 mg
Milli-Q water systemEMD Millipore Corp.Z00QSV001Ultrapure Water
HEPESFisher ScientificBP310-500500 g
EquipmentĀ 
Poseidon In situ specimen holderProtochips, Inc.Ā FEI compatible
FEI Spirit BioTwin TEMFEI Co.120 kV
Eagle 2k HS CCD cameraFEI Co.10Ā Ć…/pixel sampling at 30,000X
Gatan 655 Dry pump stationGatan, Inc.Pump holder tip to 10-6Ā range
PELCO easiGlow, glow discharge unitTed Pella, Inc.Ā Negative polarity mode
Isotemp heated stir plateFisher ScientificHeat to 150 ĀŗC for 1.5 hr

References

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  1. Zhou, Z. H. Towards atomic resolution structural determination by single-particle cryo-electron microscopy. Curr. Opin. Struct. Biol. 18, 218-228 (2008).
  2. Wolf, M., Garcea, R. L., Grigorieff, N., Harrison, S. C. Subunit interactions in bovine papillom....

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Tags

In Situ TEMBiological AssembliesLiquid EnvironmentMicrofluidic HolderAffinity CaptureRotavirus DLPsTEM ImagingVirus VisualizationNanoparticle TrackingElectron Microscopy

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