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In This Article

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

Summary

This paper describes how polarization-sensitive two-photon microscopy could be applied to characterize the local organization within label-free amyloid superstructures-spherulites. It also describes how to prepare and measure the sample, assemble the required setup, and analyze the data to obtain information about the local organization of amyloid fibrils.

Abstract

Compared to its one-photon counterpart, two-photon excitation is beneficial for bioimaging experiments because of its lower phototoxicity, deeper tissue penetration, efficient operation in densely packed systems, and reduced angular photoselection of fluorophores. Thus, the introduction of polarization analysis in two-photon fluorescence microscopy (2PFM) provides a more precise determination of molecular organization in a sample compared to standard imaging methods based on linear optical processes. In this work, we focus on polarization-sensitive 2PFM (ps-2PFM) and its application in the determination of molecular ordering within complex bio-structures-amyloid spherulites. Neurodegenerative diseases such as Alzheimer's or Parkinson's are often diagnosed through the detection of amyloids-protein aggregates formed due to an impaired protein misfolding process. Exploring their structure leads to a better understanding of their creation pathway and consequently, to developing more sensitive diagnostic methods. This paper presents the ps-2PFM adapted for the determination of local fibril ordering inside the bovine insulin spherulites and spherical amyloidogenic protein aggregates. Moreover, we prove that the proposed technique can resolve the three-dimensional organization of fibrils inside the spherulite.

Introduction

Over the past decades, although there has been significant development of numerous fluorescence microscopy techniques for bioimaging of proteins and their aggregates1, only a few have been used to resolve their local ordering within the sample2,3. Fluorescence lifetime imaging microscopy4 was used to study the intrinsic structural heterogeneity of amyloid superstructures-spherulites. Moreover, quantitative determination of the local ordering inside complex and densely-packed biostructures such as spherulites could be resolved using polarization-sensitive methods<....

Protocol

1. Preparing the microscope slides with fully-grown spherulites

NOTE: See the Table of Materials for details about all materials, reagents, and equipment used in this protocol. All solutions were prepared with deionized water (18.2 MΩ·cm at 25 °C) obtained from the water purification system.

  1. Incubate the amyloid spherulites based on the protocol described by Krebs et al16. with some modifications, as described below.
    1. Weigh 10 mg of insulin powder in a 1.5 mL tube.
    2. Dissolve the powder with a 1 mL aliquot of the deionized H

Representative Results

The presented protocol provides step-by-step guidance through the preparation of amyloid superstructures for testing with ps-2PFM, construction of the microscopic system, and measurements of the proper sample. However, before the final set of measurements, it is vital to properly align the APDs with an isotropic reference, which should result in collecting a symmetrical signal of similar shape and intensity on both detectors (Figure 4C). Even minimal differences between the intensities measu.......

Discussion

Polarization-sensitive two-photon microscopy is a valuable tool for studying the local ordering of fibrils inside the amyloid superstructures, requiring only small modifications of the standard multiphoton setup. Since it operates on nonlinear optical phenomena, reduced angular photo-selection and enhanced axial resolution can be achieved compared to one-photon excited fluorescence microscopy methods. In addition, it leads to lower light scattering, lower phototoxicity, and deeper sample penetration when compared to the .......

Disclosures

The authors have no conflicts of interest to disclose.

Acknowledgements

This work was supported by Sonata Bis 9 project (2019/34/E/ST5/00276) financed by National Science Centre in Poland.

....

Materials

NameCompanyCatalog NumberComments
Sample preparation
Coverslips, 24 x 24 mmChemland04-298.202.04
DPX mountant for histologySigma-Aldrich6522Slide mountant
Eppendorf Safe-Lock tubes, 1.5 mL, polypropyleneChemland02-63102
Eppendorf ThermoMixer CEppendorfUsed for spherulite incubation
HLP 5UV Water purification systemHydrolabSource of dionized water used in sample preparation
Hydrochloric acid (≥37%, APHA ≤10),Sigma-Aldrich30721-M
Insulin powder from the bovine pancreas (≥25 units/mg (HPLC))Sigma-AldrichI5500
Methanol (HPLC grade)Sigma-Aldrich270474
Microscope slides with a concave, 76 x 26 x 1 mmChemland04-296.202.09
Olympus BX60OlympusPolarized Optical Microscope used in Figure 2
PTFE thread seal tape, 12 mm x 12 mm x 0.1 mm, 60 gm2ChemlandVIT131097
Microscope ps-2PFM setup
Chameleon Ultra IICoherent
FELH0800 - Ø25.0 mm Longpass FilterThorlabs
FESH0700 - Ø25.0 mm Shortpass FilterThorlabs
IDQ100 photon-counting avalanche photodiodes ID Quantique
Multiphoton short-pass emission filter 720 nm Semrock
Mounted Achromatic Half-Wave Plate, 690-1200 nmThorlabs
Nikon Plan Apo Oil Immersion 100x/1.4 NANikon
piezo 3D stagePiezosystem Jena
Polarizing BeamsplitterThorlabs
S130C - Slim Photodiode Power Sensor, Si, 400 - 1100 nm, 500 mWThorlabs
Software
LabView 2018National InstrumentsVersion 18.0.1f2
Matplotlib libraryVersion 3.3.2
NumPy libraryVersion 1.19.2
SciPy libraryVersion 1.5.2
Spyder Python 3 IDEVersion 4.1.5

References

  1. Petazzi, R. A., Aji, A. K., Chiantia, S., Giraldo, J., Ciruela, F. . Progress in Molecular Biology and Translational Science. 169, 1-41 (2020).
  2. Kress, A., et al. Probing orientational behavior of MHC class I protein a....

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Polarization sensitive Two photon MicroscopyAmyloidProtein AggregatesAlzheimer s DiseaseType 2 DiabetesNonlinear Optical PhenomenaAxial ResolutionPhototoxicityTissue PenetrationMolecular OrganizationSpherulitesNeurodegenerative DiseasesProtein Misfolding

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