Abstract:
:In fluctuation-based optical nanoscopy, investigating high-density labeled subcellular structures with high fidelity has been a significant challenge. In this study, based on super-resolution radial fluctuation (SRRF) microscopy, the joint tagging (JT) strategy is employed to enable fast high-density nanoscopic imaging and tracking. In fixed cell experiment, multiple types of quantum dots with distinguishable fluorescence spectra are jointly tagged to subcellular microtubules. In each spectral channel, the decrease in labeling density guarantees the high-fidelity super-resolution reconstruction using SRRF microscopy. Subsequently, the combination of all spectral channels achieves high-density super-resolution imaging of subcellular microtubules with a resolution of ~62 nm using JT assisted SRRF technique. In the live-cell experiment, 3-channel JT is utilized to track the dynamic motions of high-density toxin-induced lipid clusters for 1 minute, achieving the simultaneous tracking of many individual toxin-induced lipid clusters spatially distributed significantly below the optical diffraction limit in living cells.
journal_name
J Biophotonicsjournal_title
Journal of biophotonicsauthors
Zeng Z,Ma J,Xi P,Xu Cdoi
10.1002/jbio.201800020subject
Has Abstractpub_date
2018-09-01 00:00:00pages
e201800020issue
9eissn
1864-063Xissn
1864-0648journal_volume
11pub_type
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