Method Article

Conducting Multiple Imaging Modes with One Fluorescence Microscope

DOI:

10.3791/58320

October 28th, 2018

In This Article

Summary

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Here we present a practical guide of building an integrated microscopy system, which merges conventional epi-fluorescent imaging, single-molecule detection-based super-resolution imaging, and multi-color single-molecule detection, including single-molecule fluorescence resonance energy transfer imaging, into one set-up in a cost-efficient way.

Abstract

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Fluorescence microscopy is a powerful tool to detect biological molecules in situ and monitor their dynamics and interactions in real-time. In addition to conventional epi-fluorescence microscopy, various imaging techniques have been developed to achieve specific experimental goals. Some of the widely used techniques include single-molecule fluorescence resonance energy transfer (smFRET), which can report conformational changes and molecular interactions with angstrom resolution, and single-molecule detection-based super-resolution (SR) imaging, which can enhance the spatial resolution approximately ten to twentyfold compared to diffraction-limited microscopy. Here we present a customer-designed integrated system, which merges multiple imaging methods in one microscope, including conventional epi-fluorescent imaging, single-molecule detection-based SR imaging, and multi-color single-molecule detection, including smFRET imaging. Different imaging methods can be achieved easily and reproducibly by switching optical elements. This set-up is easy to adopt by any research laboratory in biological sciences with a need for routine and diverse imaging experiments at a reduced cost and space relative to building separate microscopes for individual purposes.

Introduction

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Fluorescence microscopes are important tools for the modern biological science research and fluorescent imaging is routinely performed in many biology laboratories. By tagging biomolecules of interest with fluorophores, we can directly visualize them under the microscope and record the time-dependent changes in localization, conformation, interaction, and assembly state in vivo or in vitro. Conventional fluorescence microscopes have a diffraction-limited spatial resolution, which is ~200 - 300 nm in the lateral direction and ~500 - 700 nm in the axial direction1,2, and are, therefore, limited....

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Protocol

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1. Microscope Design and Assembly

  1. Excitation path
    NOTE: The excitation path includes lasers, differential interference contrast (DIC) components, the microscope body, and its illumination arm.
    1. Prepare a vibration-isolated optical table. For example, a structural damping table of 48 x 96 x 12’’ gives enough space for all the components.
      NOTE: Build the set-up in a room with temperature control (e.g., 21.4 ± 0.55 °C). Temperature stability is critical to maintaining the optical alignment.
    2. Install a microscope body that is equipped with an illumination arm for optical fiber ....

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Results

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This microscope allows flexible and reproducible switching between different imaging methods. Here we show sample images collected with each imaging module.

Figure 5D demonstrates the PSF of the blinking-on molecule during the SR acquisition. Thousands of such images are reconstructed to generate the final SR image (Figure 5E). Figure 5E sh.......

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Discussion

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This hybrid microscope system eliminates the need to purchase multiple microscopes. The total cost for all parts, including the optical table, table installation labor, software, and workstation, is about $230,000. Custom-machined parts, including the mag lens and 3-D lens, cost around $700 (the cost depends on the actual charges at different institutes). Typical commercially available integrated systems for single-molecule detection-based SR microscopy cost more than $300,000 ~ 400,000 and are not readily available for .......

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Disclosures

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The authors have nothing to disclose.

Acknowledgements

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J.F. acknowledges support from the Searle Scholars Program and the NIH Director's New Innovator Award. The authors acknowledge useful suggestions from Paul Selvin's lab (University of Illinois, Urbana-Champaign) for positioning the 3-D lens.

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Materials

List of materials used in this article
NameCompanyCatalog NumberComments
Nikon Ti-E microscope standNikonTi-E
Objective lensNikon100X NA 1.49 CFI HP TIRF
Microscopy imaging softwareNikonNIS-Elements Advanced Research/HCHC includes "JOBS" module, the programmed acquisition module being used for SR imaging.
The illumination armNikonTi-TIRF-EM Motorized Illuminator Unit MThis arm has a slot for a magnification lens
Analyze blockNikonTi-AThis is installed in the filter turret.
Z-drift correction systemNikonPFSThis system is composed by the stepmotor on the objective nosepiece, IR LED, and a detector.
Optical table topTMC783-655-02R
Optical table basesTMC14-426-35
647 nm laserCobolt90346 (0647-06-01-0120-100)Modulated Laser Diode 647nm 120mW incl. laser head, CDRH control box, USB cable and PSU (Power Supply Unit)
561 nm laserCoherent1280721OBIS 561nm LS 150mW Laser System
488 nm laserCobolt90308 (0488-06-01-0060-100)Modulated Laser Diode 488nm 60mW incl. laser head, CDRH control box, USB cable and PSU (Power Supply Unit)
405 nm laserCrystalaserDL405-025-O405 (+/-5)nm, 25mW, Circular , M2 <1.3, Low Noise, CW, TTL up to 20MHz. 2 BNC connectors for TTL & Analog adjust
Heat sinkCobolt11658 (HS-03)Two units, Heat sink without fan HS-03, Heat sink for 647 nm and 488 nm lasers
Heat sinkCoherent1193289Obis heat sink with fan, 165 x 50 x 50 mm for the 561 nm laser
CAB-USB-miniUSBCobolt10908Two units, communication cable for 647 nm and 488 nm lasers
aluminum for height adjustmentMcMaster-Carr9146T35Multipurpose 6061 Aluminum, Rectangular Bar, 4MM X 40MM, 1' Long for raising 561 nm laser
aluminum for height adjustmentMcMaster-Carr8975K248Multipurpose 6061 Aluminum, 1-1/4" Thick X 3" Width X 1' Length for raising 405 nm laser
BNC cableL-comCC58C-6RG58C Coaxial Cable, BNC Male / Male, 6.0 ft
BNC adapterL-comBA1087Coaxial Adapter, BNC Bulkhead, Grounded
SMA to BNC AdapterHODSMA-870Cobolt MLD lasers have SMA interface, so this adapter is used for BNC connection.
SMB to BNC AdapterFairview MicrowaveFMC1638316-12SMB Plug to BNC Female Bulkhead Cable RG316 Coax in 12 Inch for Coherent Obis lasers
Data Acquisition CardNational InstrumentsPCI-672313-Bit, 32 Channels, 800 kS/s Analog Output Device for controlling lasers, DIC LED, and etc
Barrier Filter Wheel controllerSutter InstrumentLambda 10-BOptical Filter Changer
Emission SplitterCairnOptoSplit III
Dichroic beamsplitterChromaT640LPXR-UF2Dichroic beamsplitter separating red emission from green emission in OptoSplit III
Dichroic beamsplitterChromaT565LPXR-UF2Dichroic beamsplitter separating green & red emission from blue emission in OptoSplit III
Emission filterChromaET700/75MTwo units, Emission filter for red emission (like Alexa Fluor 647) in OptoSplit III as well as in the Barrier filter wheel
Emission filterChromaET595/50MTwo units, Emission filter for yellow/green emission (like Cy3B) in OptoSplit III as well as in the Barrier filter wheel
Emission filterChromaET525/50MTwo units, Emission filter for blue emission(like Alexa Fluor 488/GFP) in OptoSplit III as well as in the Barrier filter wheel
Emission filterSemrockFF02-447/60-25Emission filter for violet emission (like DAPI/Alexa Fluor 405), installed in the Barrier filter wheel
Dichroic beamsplitterChromazt405/488/561/647/752rpc-UF3Multiband dichroic beam splitter for 647, 561, 488, and 405 nm laser excitations inside of the microscope body
DAPI Filter setChroma49000installed in the microscope body
Nikon laser/TIRF filtercubeChroma91032
590 long pass filterChromaT590LPXR-UF1for combining 647 nm laser and 561 nm laser
525 long pass filterChromaT525LPXR-UF1for combining already combined 647 nm and 561nm lasers with 488 nm laser
470 long pass filterChromaT470LPXR-UF1for combining already combined 647 nm, 561 nm and 488 nm lasers with 405 nm laser
Laser clean-up filter (647)Chromazet640/20xfor cleaning up other wavelengths from the 647 nm laser
Laser clean up filter (488)SemrockLL01-488-25for cleaning up other wavelengths from the 488 nm laser
LED light sourceExcelitasX-Cite120LEDused only for DAPI imaging
Mirror mountNewportSU100-F3K
Optical postsNewportPS-2
Clamping forkNewportPS-F
Power MeterNewportPMKITFor measuring laser power
Dichroic beamcombiner mountEdmund Optics58-872C-Mount Kinematic Mount, for holding dichroic beamcombiners in the laser excitation assembly
Retaining ringThorlabsCMRRused for dichroic beamcombiner mounts
Fiber Adapter PlateThorlabsSM1FCFC/PC Fiber Adapter Plate with External SM1 (1.035"-40) Thread
Z-axis translational mountThorlabsSM1ZZ-Axis Translation Mount, 30 mm Cage Compatible
Achromatic Doublet lensThorlabsAC050-008-A-MLØ5 mm, Mounted Achromatic Doublets, AR Coated: 400 - 700 nm
Cage PlateThorlabsCP1TM0930 mm Cage Plate with M9 x 0.5 Internal Threads, 8-32 Tap
Cage Assembly RodThorlabsER4Cage Assembly Rod, 4" Long, Ø6 mm
Cage Mounting BracketThorlabsCP02B30 mm Cage Mounting Bracket
Single mode optical fiberThorlabsP5-405BPM-FC-2Patch Cable, PM, FC/PC to FC/APC, 405 nm, Panda, 2 m
Multi mode optical fiberThorlabsM42L01Ø50 µm, 0.22 NA, FC/PC-FC/PC Fiber Patch Cable, 1 m
Achromatic Doublet lens (mag lens)ThorlabsACN127-025-AACN127-025-A - f=-25.0 mm, Ø1/2" Achromatic Doublet, ARC: 400-700 nm , a concave lens in the "mag lens"
Achromatic Doublet lens (mag lens)ThorlabsAC127-050-Af=50.0 mm, Ø1/2" Achromatic Doublet, ARC: 400-700 nm, a convex lens in the "mag lens"
Retaining ringThorlabsSM05PRRSM05 Plastic Retaining Ring for Ø1/2" Lens Tubes and Mounts, for "mag lens"
Nylon-tipped screwThorlabsSS3MN6M3 x 0.5 Nylon-Tipped Setscrew, 6 mm Long, for holding "3D lens"
3D lensCVI Laser OpticsRCX-25.4-50.8-5000.0-C-415-700f=10 m, rectangular cylindrical lens
EMCCD cameraAndoriXon Ultra 888
100 nm multichannel beadsThermoT7279, TetraSpeck microspheres
red dyeThermoAlexa Fluor 647
yellow-green dyeGE HealthcareCy3
green dyeGE HealthcareCy3B
blue dyeThermoAlexa Fluor 488

References

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  1. Lipson, S. G., Lipson, H., Tannhauser, D. S. Optical physics. , Cambridge University Press. Cambridge, UK; New York, NY. (1995).
  2. Török, P., Wilson, T. Rigorous theory for axial resolution in confocal microscopes. Optics Communications. 137 (1-3), 127-135 (1997).
  3. Klar, T. A., Hell, S. W.

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Tags

Fluorescence MicroscopySuper Resolution ImagingSingle Molecule FRETMulticolor DetectionEpifluorescence ImagingOptical AlignmentLaser ControlEmission Filter Wheel3D Lens InsertionData Acquisition Card

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