Journal
ANALYTICAL CHEMISTRY
Volume 93, Issue 49, Pages 16709-16717Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acs.analchem.1c04466
Keywords
-
Categories
Ask authors/readers for more resources
This study introduces a novel method for detecting DNA methylation through conformational transition to G-quadruplex, using a solution-gated field-effect transistor (SG-FET) without the need for labeled materials. The method involves grafting a dense hydrophilic polymer brush onto the SG-FET sensor surface to reduce electrical noise and achieve high signal-to-noise ratio analysis of DNA sequences.
Methylated DNA is not only a diagnostic but also a prognostic biomarker for early-stage cancer. However, sodium bisulfite sequencing as a gold standard method for detection of methylation markers has some drawbacks such as its time-consuming and labor-intensive procedures. Therefore, simple and reliable methods are required to analyze DNA sequences with or without methylated residues. Herein, we propose a simple and direct method for detecting DNA methylation through its conformation transition to G-quadruplex using a solution-gated field-effect transistor (SG-FET) without using labeled materials. The BCL-2 gene, which is involved in the development of various human tumors, contains G-rich segments and undergoes a conformational change to G-quadruplex depending on the K-1 concentration. Stacked G-quadruplex strands move close to the SG-FET sensor surface, resulting in large electrical signals based on intrinsic molecular charges. In addition, a dense hydrophilic polymer brush is grafted using surface-initiated atom transfer radical polymerization onto the SG-FET sensor surface to reduce electrical noise based on nonspecific adsorption of interfering species. In particular, control of the polymer brush thickness induces electrical signals based on DNA molecular charges in the diffusion layer, according to the Debye length limit. A platform based on the SG-FET sensor with a well-defined polymer brush is suitable for in situ monitoring of methylated DNA and realizes a point-of-care device with a high signal-to-noise ratio and without the requirement for additional processes such as bisulfite conversion and polymerase chain reaction.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available