Label-free nanoscale mapping of intracellular organelle chemistry

被引:9
作者
Greaves, George E. [1 ]
Kiryushko, Darya [1 ,2 ,3 ]
Auner, Holger W. [4 ]
Porter, Alexandra E. [2 ,3 ]
Phillips, Chris C. [1 ]
机构
[1] Imperial Coll London, Dept Phys, Expt Solid State Grp, London, England
[2] Imperial Coll London, Dept Mat, London, England
[3] Imperial Coll London, London Ctr Nanotechnol, London, England
[4] Imperial Coll London, Hugh & Josseline Langmuir Ctr Myeloma Res, Dept Immunol & Inflammat, London, England
基金
英国工程与自然科学研究理事会;
关键词
FIELD OPTICAL MICROSCOPY; EXTRAMEDULLARY PLASMACYTOMA; MULTIPLE-MYELOMA; PROTEIN; SPECTROSCOPY; GROWTH;
D O I
10.1038/s42003-023-04943-7
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The ability to image cell chemistry at the nanoscale is key for understanding cell biology, but many optical microscopies are restricted by the similar to(200-250)nm diffraction limit. Electron microscopy and super-resolution fluorescence techniques beat this limit, but rely on staining and specialised labelling to generate image contrast. It is challenging, therefore, to obtain information about the functional chemistry of intracellular components. Here we demonstrate a technique for intracellular label-free chemical mapping with nanoscale (similar to 30 nm) resolution. We use a probe-based optical microscope illuminated with a mid-infrared laser whose wavelengths excite vibrational modes of functional groups occurring within biological molecules. As a demonstration, we chemically map intracellular structures in human multiple myeloma cells and compare the morphologies with electron micrographs of the same cell line. We also demonstrate label-free mapping at wavelengths chosen to target the chemical signatures of proteins and nucleic acids, in a way that can be used to identify biochemical markers in the study of disease and pharmacology.
引用
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页数:7
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