Combining Qdot Nanotechnology and DNA Nanotechnology for Sensitive Single-Cell Imaging

© 2020 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Bibliographische Detailangaben
Veröffentlicht in:Advanced materials (Deerfield Beach, Fla.). - 1998. - 32(2020), 30 vom: 17. Juli, Seite e1908410
1. Verfasser: Zhou, Wen (VerfasserIn)
Weitere Verfasser: Han, Yan, Beliveau, Brian J, Gao, Xiaohu
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2020
Zugriff auf das übergeordnete Werk:Advanced materials (Deerfield Beach, Fla.)
Schlagworte:Journal Article DNA nanotechnology imaging multiplexing quantum dots single cells DNA 9007-49-2
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520 |a Immunohistochemistry (IHC) can provide detailed information about protein expression within the cell microenvironment and is one of the most common techniques in biology and medicine due to the broad availability of highly specific antibodies and well-established bioconjugation methods for modification of these antibodies with chromogens and fluorophores. Despite recent advances in this field, it remains challenging to simultaneously achieve high multiplexing, sensitivity, and throughput in single-cell profiling experiments. Here, the combination of two powerful technologies is reported, quantum dot and signal amplification by exchange reaction (QD-SABER), for sensitive and multiplexed imaging of endogenous proteins. Compared to the conventional IHC process using dye-labeled secondary antibodies (which already has a built-in signal amplification mechanism), QD-SABER provides an additional 7.6-fold signal amplification. In addition, the DNA hybridization-based IHC can be rapidly removed to regenerate the sample for subsequent cycles of immunostaining (>10 cycles), greatly expanding the multiplexing capability 
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700 1 |a Han, Yan  |e verfasserin  |4 aut 
700 1 |a Beliveau, Brian J  |e verfasserin  |4 aut 
700 1 |a Gao, Xiaohu  |e verfasserin  |4 aut 
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