Multi-molecular hyperspectral PRM-SRS microscopy.
Wenxu ZhangYajuan LiAnthony A FungZhi LiHongje JangHonghao ZhaXiaoping ChenFangyuan GaoJane Y WuHuaxin ShengJunjie YaoDorota Skowronska-KrawczykSanjay JainLingyan ShiPublished in: Nature communications (2024)
Lipids play crucial roles in many biological processes. Mapping spatial distributions and examining the metabolic dynamics of different lipid subtypes in cells and tissues are critical to better understanding their roles in aging and diseases. Commonly used imaging methods (such as mass spectrometry-based, fluorescence labeling, conventional optical imaging) can disrupt the native environment of cells/tissues, have limited spatial or spectral resolution, or cannot distinguish different lipid subtypes. Here we present a hyperspectral imaging platform that integrates a Penalized Reference Matching algorithm with Stimulated Raman Scattering (PRM-SRS) microscopy. Using this platform, we visualize and identify high density lipoprotein particles in human kidney, a high cholesterol to phosphatidylethanolamine ratio inside granule cells of mouse hippocampus, and subcellular distributions of sphingosine and cardiolipin in human brain. Our PRM-SRS displays unique advantages of enhanced chemical specificity, subcellular resolution, and fast data processing in distinguishing lipid subtypes in different organs and species.
Keyphrases
- high resolution
- induced apoptosis
- single molecule
- mass spectrometry
- high density
- cell cycle arrest
- high throughput
- gene expression
- optical coherence tomography
- endothelial cells
- high speed
- machine learning
- endoplasmic reticulum stress
- oxidative stress
- cell death
- computed tomography
- signaling pathway
- liquid chromatography
- cell proliferation
- low density lipoprotein
- quantum dots
- label free
- monte carlo
- cognitive impairment
- data analysis
- prefrontal cortex