TY - JOUR
T1 - Versatile naphthalimide tetrazines for fluorogenic bioorthogonal labelling
AU - Graziotto, Marcus E.
AU - Adair, Liam D.
AU - Kaur, Amandeep
AU - Vérité, Pauline
AU - Ball, Sarah R.
AU - Sunde, Margaret
AU - Jacquemin, Denis
AU - New, Elizabeth J.
N1 - Funding Information:
The authors would like to acknowledge the Australian Research Council (DP180101353, DP180101897 and DP200102463) for funding, the Westpac Scholars Trust for a Research Fellowship (EJN), the University of Sydney for a SOAR Fellowship (EJN) a USyd Fellowship (AK), and the John A Lamberton Scholarship (MEG), and the Australian Government for Research Training Program Scholarships (MEG, SRB). We acknowledge the scientific and technical assistance of Sydney Analytical, the Mass Spectrometry Facility at the School of Chemistry and the Australian Microscopy and Microanalysis Research Facility at the Australian Centre for Microscopy and Microanalysis (ACMM). PMV and DJ thank the ANR for support in the frame-work of the GeDeMi grant. This research used the computational resources of CCIPL (Centre de Calcul Intensif des Pays de la Loire).
Publisher Copyright:
© The Royal Society of Chemistry.
PY - 2021/10
Y1 - 2021/10
N2 - Fluorescent probes for biological imaging have revealed much about the functions of biomolecules in health and disease. Fluorogenic probes, which are fluorescent only upon a bioorthogonal reaction with a specific partner, are particularly advantageous as they ensure that fluorescent signals observed in biological imaging arise solely from the intended target. In this work, we report the first series of naphthalimide tetrazines for bioorthogonal fluorogenic labelling. We establish that all of these compounds can be used for imaging through photophysical, analytical and biological studies. The best candidate was Np6mTz, where the tetrazine ring is appended to the naphthalimide at its 6-position via a phenyl linker in a meta configuration. Taking our synthetic scaffold, we generated two targeted variants, LysoNpTz and MitoNpTz, which successfully localized within the lysosomes and mitochondria respectively, without the requirement of genetic modification. In addition, the naphthalimide tetrazine system was used for the no-wash imaging of insulin amyloid fibrils in vitro, providing a new method that can monitor their growth kinetics and morphology. Since our synthetic approach is simple and modular, these new naphthalimide tetrazines provide a novel scaffold for a range of bioorthogonal tetrazine-based imaging agents for selective staining and sensing of biomolecules. This journal is
AB - Fluorescent probes for biological imaging have revealed much about the functions of biomolecules in health and disease. Fluorogenic probes, which are fluorescent only upon a bioorthogonal reaction with a specific partner, are particularly advantageous as they ensure that fluorescent signals observed in biological imaging arise solely from the intended target. In this work, we report the first series of naphthalimide tetrazines for bioorthogonal fluorogenic labelling. We establish that all of these compounds can be used for imaging through photophysical, analytical and biological studies. The best candidate was Np6mTz, where the tetrazine ring is appended to the naphthalimide at its 6-position via a phenyl linker in a meta configuration. Taking our synthetic scaffold, we generated two targeted variants, LysoNpTz and MitoNpTz, which successfully localized within the lysosomes and mitochondria respectively, without the requirement of genetic modification. In addition, the naphthalimide tetrazine system was used for the no-wash imaging of insulin amyloid fibrils in vitro, providing a new method that can monitor their growth kinetics and morphology. Since our synthetic approach is simple and modular, these new naphthalimide tetrazines provide a novel scaffold for a range of bioorthogonal tetrazine-based imaging agents for selective staining and sensing of biomolecules. This journal is
UR - http://www.scopus.com/inward/record.url?scp=85116940248&partnerID=8YFLogxK
U2 - 10.1039/d1cb00128k
DO - 10.1039/d1cb00128k
M3 - Article
C2 - 34704054
AN - SCOPUS:85116940248
SN - 2633-0679
VL - 2
SP - 1491
EP - 1498
JO - RSC Chemical Biology
JF - RSC Chemical Biology
IS - 5
ER -