Author
Listed:
- Jing Yang
(Massachusetts General Hospital/Harvard Medical School, Room 2301, Building 149, Charlestown)
- Wei Yin
(Massachusetts General Hospital/Harvard Medical School, Room 2301, Building 149, Charlestown)
- Richard Van
(University of Oklahoma)
- Keyi Yin
(Massachusetts General Hospital/Harvard Medical School, Room 2301, Building 149, Charlestown)
- Peng Wang
(Massachusetts General Hospital/Harvard Medical School, Room 2301, Building 149, Charlestown)
- Chao Zheng
(Massachusetts General Hospital/Harvard Medical School, Room 2301, Building 149, Charlestown)
- Biyue Zhu
(Massachusetts General Hospital/Harvard Medical School, Room 2301, Building 149, Charlestown)
- Kathleen Ran
(Massachusetts General Hospital/Harvard Medical School, Room 2301, Building 149, Charlestown)
- Can Zhang
(Massachusetts General Hospital and Harvard Medical School)
- Mohanraja Kumar
(Massachusetts Institute of Technology)
- Yihan Shao
(University of Oklahoma)
- Chongzhao Ran
(Massachusetts General Hospital/Harvard Medical School, Room 2301, Building 149, Charlestown)
Abstract
Turn-on fluorescence imaging is routinely studied; however, turn-on chemiluminescence has been rarely explored for in vivo imaging. Herein, we report the design and validation of chemiluminescence probe ADLumin-1 as a turn-on probe for amyloid beta (Aβ) species. Two-photon imaging indicates that ADLumin-1 can efficiently cross the blood–brain barrier and provides excellent contrast for Aβ plaques and cerebral amyloid angiopathy. In vivo brain imaging shows that the chemiluminescence signal of ADLumin-1 from 5-month-old transgenic 5xFAD mice is 1.80-fold higher than that from the age-matched wild-type mice. Moreover, we demonstrate that it is feasible to further dually-amplify signal via chemiluminescence resonance energy transfer (DAS-CRET) using two non-conjugated smart probes (ADLumin-1 and CRANAD-3) in solutions, brain homogenates, and in vivo whole brain imaging. Our results show that DAS-CRET can provide a 2.25-fold margin between 5-month-old 5xFAD mice and wild type mice. We believe that our strategy could be extended to other aggregating-prone proteins.
Suggested Citation
Jing Yang & Wei Yin & Richard Van & Keyi Yin & Peng Wang & Chao Zheng & Biyue Zhu & Kathleen Ran & Can Zhang & Mohanraja Kumar & Yihan Shao & Chongzhao Ran, 2020.
"Turn-on chemiluminescence probes and dual-amplification of signal for detection of amyloid beta species in vivo,"
Nature Communications, Nature, vol. 11(1), pages 1-14, December.
Handle:
RePEc:nat:natcom:v:11:y:2020:i:1:d:10.1038_s41467-020-17783-4
DOI: 10.1038/s41467-020-17783-4
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