Carbon dot-based fluorescent antibody nanoprobes as brain tumour glioblastoma diagnostics

被引:17
作者
Ghirardello, Mattia [1 ]
Shyam, Radhe [1 ]
Liu, Xia [2 ]
Garcia-Millan, Teodoro [1 ]
Sittel, Imke [1 ]
Ramos-Soriano, F. Javier [1 ]
Kurian, Kathreena [2 ]
Galan, M. Carmen [1 ]
机构
[1] Univ Bristol, Sch Chem, Bristol, Avon, England
[2] Univ Bristol, Southmead Hosp, Bristol Med Sch, Publ Hlth Sci, Bristol, Avon, England
来源
NANOSCALE ADVANCES | 2022年 / 4卷 / 07期
基金
欧洲研究理事会; 英国工程与自然科学研究理事会;
关键词
PROBES; CELLS;
D O I
10.1039/d2na00060a
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
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.
引用
收藏
页码:1770 / 1778
页数:9
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