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In This Article

  • Summary
  • Abstract
  • Introduction
  • Protocol
  • Results
  • Discussion
  • Disclosures
  • Acknowledgements
  • Materials
  • References
  • Reprints and Permissions

Summary

We developed an open-source Micro-Manager plugin, which enables live-view observation of fluorescent dipoles on a structured illumination microscope. The plugin supports observation of both 2D and 3D dipole orientation.

Abstract

Fluorescence polarization microscopy (FPM) can image the position and dipole orientation of fluorophores. Despite the achievements of super-resolution fluorescence polarization microscopy, their reliance on post-acquisition hinders real-time observation. Polarized structured illumination microscopy (pSIM) offers super-resolution imaging of fluorescent dipoles with fast imaging speed and is well-suited for live-cell applications. We developed an open-source implementation for real-time reconstruction of polarization images and display of the fluorescent dipoles. Additionally, we extended the method to achieve 3D orientation mapping (3DOM), broadening its utility for complex biological studies.Furthermore, we have presented a thorough introduction to extending an existing SIM microscope on polarization imaging and provided a detailed configuration guide of Micro-Manager 2.0 to control the microscope, enabling real-time preview of polarized imaging. Additionally, we have provided the MATLAB code for full reconstructionencompassing both pSIM and 3DOM. This comprehensive guide aims to assist beginners in quickly mastering and easily getting started with the operations.

Introduction

Fluorescence polarization microscopy (FPM) has emerged as a powerful technique for simultaneously imaging both the position and dipole orientation of fluorophores, offering profound insights into biological imaging1,2. By facilitating direction observation of biomolecules' orientations, FPM unveils the intricate arrangement of macro-molecules such as actin3,4,5, microtubule5, septin6, DNA filament7-9

Protocol

1. Extending an existing structured illumination microscope for polarization imaging

  1. Prepare a SIM microscope.
    NOTE:Β We assume that readers have a certain foundation in microscope setup and already possess a structured light microscope. If you lack relevant experience, refer to this paper, which provides a detailed description of how to build a SIM microscope16. The polarization control unit of "HWP+WQP+LCVR" can be replaced by a pizza vortex wave plate in our pSIM work5 or a pizza half wave plate17.
  2. Measure polarization extinction ratios ....

Results

The pSIM method can be performed on SIM microscopes based on the interference using s-polarized laser beams. s-polarization interference is the mostly widely used type of SIM and generates high-contrast illumination stripes. The academic prototype of a microscope setup is included in the original work of pSIM5. Briefly introduced in Figure 1, a spatial light modulator (SLM) generates the Β±1 order of diffractive beams and a pizza h.......

Discussion

In our study, we developed a plugin that allows real-time preview of two polarization imaging techniques, pSIM and 3DOM. Both technologies can be performed in an existing SIM system with slight modification. We have provided the detailed steps to install the pSIM and 3DOM microscope and set up Micro-Manager to control the microscope and demonstrate how to obtain the live-view polarization results. The experimental results include the actin filament imaged by pSIM and Ξ»-DNA imaged by 3DOM.The orientation of the phall.......

Disclosures

The authors declare no conflicts of interest.

Acknowledgements

This work was supported by the National Key Research and Development Program of China (2022YFC3401100).

....

Materials

NameCompanyCatalog NumberComments
100 nm Fluorescent beadsInvitrogenF8801
4% Formaldehyde solutionInvitrogenR37814
CameraTucsenDhyana 400BSI V3https://www.tucsen.com/download-software/
Denture base materials (Type I Thermally setting type, liquid)New Century DentalN/A
Dulbecco’s Modified Eagle’s MediumGibcoC11995500BT
Eclipse TE2000 Inverted MicroscopeNikonTE2000 E
Fetal Bovine SerumGibco10099141C
MATLAB R2019bMathWorksVersion R2019bhttps://ww2.mathworks.cn/downloads/
MetroCon V4.0KopinVersion 4.0Software of Spatial light modulator
Micro-Manager 2.0μΜanagerVersion 2.0Download Micro-Manager Latest Release
MS-2000 XYZ Automated StageApplied Scientific InstrumentationMIM3https://www.asiimaging.com/support/downloads/usb-support-on-ms-2000-wk-controllers/
myDAQNational Instruments781325-01Software and Driver Downloads - NI
OBIS 561 nm LS 20 mW LaserCoherent1325777
Phalloidin-AF568InvitrogenA12380
Phosphate buffered salineCorning21-040-CV
Poly Methyl MethacrylateSolarbioM9810
ProLong DiamondInvitrogenP36980
Spatial light modulatorKopinSXGA-12
SYTOX orange nucleic acid stainInvitrogenS11368
Triton X-100InvitrogenHFH10
TrypsinGibco25200056
Ξ»-DNAInvitrogenS11368

References

  1. Zhanghao, K., Gao, J., Jin, D., Zhang, X., Xi, P. Super-resolution fluorescence polarization microscopy. J Innov Opt Health Sci. 11 (01), 1730002 (2018).
  2. Alonso, M. A., Brasselet, S. Polarization microscopy: from ensemble structural imaging to single-molecule 3D orientation and localization microscopy. Optica. 10 (11), 1486-1510 (2023).
  3. Valades Cruz, C. A. et al. Quantitative nanoscale imaging of orientational order in biological filaments by polarized superresolution microscopy. Pro Natl Acad Sci USA. 113 (7), E820-828 (2016).
  4. Zhanghao, K. et al. Super-reso....

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Open sourceMicro ManagerFluorescence Polarization MicroscopyFPMSuper resolution ImagingPolarized Structured Illumination MicroscopyPSIMReal time ReconstructionPolarization ImagesFluorescent Dipoles3D Orientation Mapping3DOMSIM MicroscopeMATLAB CodeImaging Guide

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