Ultrasensitive detection of 5-hydroxymethylcytosine in genomic DNA using a graphene-based sensor modified with biotin and gold nanoparticlesShow others and affiliations
2024 (English)In: Materials Today Bio, E-ISSN 2590-0064, Vol. 27, article id 101123Article in journal (Refereed) Published
Abstract [en]
Ten-eleven translocation (TET) proteins orchestrate deoxyribonucleic acid (DNA) methylation-demethylation dynamics by oxidizing 5-methylcytosine to 5-hydroxymethylcytosine (5hmC) and are frequently inactivated in various cancers. Due to the significance of 5hmC as an epigenetic biomarker for cancer diagnosis, pathogenesis, and treatment, its rapid and precise quantification is essential. Here, we report a highly sensitive electrochemical method for quantifying genomic 5hmC using graphene sheets that were electrochemically exfoliated and functionalized with biotin and gold nanoparticles (Bt-AuNPs) through a single-step electrical method. The attachment of Bt-AuNPs to graphene enhances the specificity of 5hmC-containing DNA and augments the oxidation of 5hmC to 5-formylcytosine in DNA. When coupled to a gold electrode, the Bt-AuNP-graphene-based sensor exhibits exceptional sensitivity and specificity for detecting 5hmC, with a detection limit of 63.2 fM. Furthermore, our sensor exhibits a remarkable capacity to measure 5hmC levels across a range of biological samples, including preclinical mouse tissues with varying 5hmC levels due to either TET gene disruption or oncogenic transformation, as well as human prostate cancer cell lines. Therefore, our sensing strategy has substantial potential for cancer diagnostics and prognosis.
Place, publisher, year, edition, pages
Elsevier BV , 2024. Vol. 27, article id 101123
Keywords [en]
5hmC, Cancer biomarker, Electrochemical quantification, Gold nanoparticle, Graphene functionalization, Graphene-based sensor
National Category
Cancer and Oncology
Identifiers
URN: urn:nbn:se:kth:diva-348763DOI: 10.1016/j.mtbio.2024.101123ISI: 001257546000001Scopus ID: 2-s2.0-85196002203OAI: oai:DiVA.org:kth-348763DiVA, id: diva2:1878673
Note
QC 20240627
2024-06-272024-06-272024-07-15Bibliographically approved