Abstract
The development of efficient and sensitive tools for the detection of brain cancer in patients is of the utmost importance particularly because many of these tumours go undiagnosed until the disease has advanced and when treatment is less effective. Current strategies employ antibodies (Abs) to detect Glial Fibrillary Acid Protein (GFAP) in tissue samples, since GFAP is unique to the brain and not present in normal peripheral blood, and it relies on fluorescent reporters. Herein we describe a low cost, practical and general method for the labelling of proteins and antibodies with fluorescent carbon dots (CD) to generate diagnostic probes that are robust, photostable and applicable to the clinical setting. The two-step protocol relies on the conjugation of a dibenzocyclooctyne (DBCO)-functionalised CD with azide functionalised proteins by combining amide conjugation and strain promoted alkyne-azide cycloaddition (SPAAC) ligation chemistry. The new class of Ab-CD conjugates developed using this strategy was successfully used for the immunohistochemical staining of human brain tissues of patients with glioblastoma (GBM) validating the approach. Overall, these novel fluorescent probes offer a promising and versatile strategy in terms of costs, photostability and applicability which can be extended to other Abs and protein systems.
Original language | English |
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Pages (from-to) | 1770-1778 |
Number of pages | 9 |
Journal | Nanoscale Advances |
Volume | 4 |
Issue number | 7 |
DOIs | |
Publication status | Published - 29 Mar 2022 |
Bibliographical note
Funding Information:The authors thank Cancer Research UK (grant number C30758/A2979). TGM thanks EPSRC BCFN EP/L016648/1/Conacyt. This research was also funded by the European Research Council (MCG), grant number ERC-COG:648239 and by the MSCA fellowship project 843720-BioNanoProbes (JRS). The authors thank Dr Katy Jepson and the Wolfson Bioimaging Facility for her assistance in this work.
Publisher Copyright:
© 2022 The Author(s).