bioRxiv · 10.1101/2021.05.18.444466
Bimodal Endocytic Probe for Three-Dimensional Correlative Light and Electron Microscopy
Abstract
Correlative light and electron microscopy (CLEM) can infer molecular, functional and dynamic information to ultrastructure by linking information of different imaging modalities. One of the main challenges, especially in 3D-CLEM, is the accurate registration of fluorescent signals to electron microscopy (EM). Here, we present fluorescent BSA-gold (fBSA-Au), a bimodal endocytic tracer as fiducial marker for 2D and 3D CLEM applications. fBSA-Au consists of colloidal gold (Au) particles stabilized with fluorescent bovine serum albumin (BSA). The conjugate is efficiently endocytosed and distributed throughout the 3D endo-lysosomal network of the cells, and has an excellent visibility both in fluorescence microscopy (FM) and EM. We demonstrate the use of fBSA-Au in several 2D and 3D CLEM applications using Tokuyasu cryosections, resin-embedded material, and cryo-EM. As a fiducial marker, fBSA-Au facilitates rapid registration of regions of interest between FM and EM modalities and enables accurate (50-150 nm) correlation of fluorescence to EM data. Endocytosed fBSA-Au benefits from a homogenous 3D distribution throughout the endosomal system within the cell, and does not obscure any cellular ultrastructure. The broad applicability and visibility in both modalities makes fBSA-Au an excellent endocytic fiducial marker for 2D and 3D (cryo-)CLEM applications.
Source connections
Explore related subjects
Keep this discovery
Explore connections, maps & timelines
Fermie, J., de Jager, L., Foster, H., Veenendaal, T., de Heus, C., van Dijk, S., ten Brink, C., Oorschot, V., Yang, L., Li, W., Muller, W., Howes, S., Carter, A., Foerster, F., Posthuma, G., Gerritsen, H., Klumperman, J., Liv, N.. 2021-05-18. Bimodal Endocytic Probe for Three-Dimensional Correlative Light and Electron Microscopy. https://doi.org/10.1101/2021.05.18.444466
Cite the original work for its findings. Save a collection to share your selection of sources.