Cathodoluminescent and Characteristic X-Ray-Emissive Rare-Earth-Doped Core/Shell Protein Labels for Spectromicroscopic Analysis of Cell Surface Receptors.
Sebastian HabermannLukas R H GerkenMathieu KociakChristian MonachonVera Maria KisslingAlexander GogosInge Katrin HerrmannPublished in: Small (Weinheim an der Bergstrasse, Germany) (2024)
Understanding the localization and the interactions of biomolecules at the nanoscale and in the cellular context remains challenging. Electron microscopy (EM), unlike light-based microscopy, gives access to the cellular ultrastructure yet results in grey-scale images and averts unambiguous (co-)localization of biomolecules. Multimodal nanoparticle-based protein labels for correlative cathodoluminescence electron microscopy (CCLEM) and energy-dispersive X-ray spectromicroscopy (EDX-SM) are presented. The single-particle STEM-cathodoluminescence (CL) and characteristic X-ray emissivity of sub-20 nm lanthanide-doped nanoparticles are exploited as unique spectral fingerprints for precise label localization and identification. To maximize the nanoparticle brightness, lanthanides are incorporated in a low-phonon host lattice and separated from the environment using a passivating shell. The core/shell nanoparticles are then functionalized with either folic (terbium-doped) or caffeic acid (europium-doped). Their potential for (protein-)labeling is successfully demonstrated using HeLa cells expressing different surface receptors that bind to folic or caffeic acid, respectively. Both particle populations show single-particle CL emission along with a distinctive energy-dispersive X-ray signal, with the latter enabling color-based localization of receptors within swift imaging times well below 2 min per μ m $\umu\text{m}$ 2 while offering high resolution with a pixel size of 2.78 nm. Taken together, these results open a route to multi-color labeling based on electron spectromicroscopy.
Keyphrases
- electron microscopy
- quantum dots
- high resolution
- metal organic framework
- highly efficient
- cell surface
- optical coherence tomography
- protein protein
- visible light
- photodynamic therapy
- amino acid
- induced apoptosis
- single molecule
- ionic liquid
- mass spectrometry
- solid phase extraction
- minimally invasive
- energy transfer
- dual energy
- gas chromatography mass spectrometry
- deep learning
- magnetic resonance imaging
- pain management
- high throughput
- cell death
- high speed
- multiple sclerosis
- convolutional neural network
- cell proliferation
- solid state
- chronic pain
- light emitting
- tandem mass spectrometry