User-Friendly Multifunctional Red-Emissive Carbon Dots for Rapid Cell Nucleus Staining via Targeting Nuclear Proteins.

Anal Chem

National Engineering Laboratory for Rice and Byproducts Further Processing, College of Food Science and Engineering, Central South University of Forestry and Technology, Changsha 410004, China.

Published: May 2024

AI Article Synopsis

  • The study introduces multifunctional red-emissive carbon dots (R-CDs) that effectively stain cell nuclei by targeting nuclear proteins, enhancing disease diagnosis and cell biology research.
  • R-CDs are easy to prepare, exhibit strong fluorescence at 635 nm, and offer advantages over traditional dyes like Hoechst and DAPI, including lower cost, better water dispersion, and stability without strict storage conditions.
  • With a quick staining time for live (3 min) and dead cells (10 s), R-CDs can distinguish between cell types while not binding to DNA, making them safe for various biological and medical applications.

Article Abstract

Cytoarchitectural staining is of great importance in disease diagnosis and cell biology research. This study developed user-friendly multifunctional red-emissive carbon dots (R-CDs) for rapid cell nucleus staining via targeting nuclear proteins. R-CDs, simply prepared by electrochemical treatment of 1,2,4-benzenetriamine, exhibit strong emission at 635 nm when excited at 507 nm. The R-CDs can rapidly stain the nucleus of human SH-SY5Y, HepG2, and HUH-7 cells with a high signal-to-noise ratio owing to fluorescence enhancement after entering the nucleus. Compared to conventional cytosolic dyes such as Hoechst and DAPI, R-CDs are cheaper, more highly dispersed in water, and more stable (requiring no stringent storage conditions). The R-CDs show stable optical properties with insignificant photobleaching over 7 days and salt resistance up to 2 M of NaCl. More importantly, R-CDs, possessing a positive charge, allow rapid staining of live cells (3 min) and dead cells (10 s) in saline. According to kinetic variation, R-CDs can distinguish live cells from dead cells. Staining exhibits high efficiency in onion epidermal cells, , , and human spermatozoa. The mechanism for efficient staining is based on their fast accumulation in the nucleus due to their small size and positive charge and strong interaction with nuclear proteins at amino acid residues of histidine and arginine, resulting in fluorescence enhancement by dozens of times. The developed R-CDs do not bind to DNA and would not cause genetic damage and will find various safe applications in biological and medical fields.

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Source
http://dx.doi.org/10.1021/acs.analchem.3c05922DOI Listing

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