AI Article Synopsis

  • The study introduces a new electrochemical bioplatform that can simultaneously detect four different types of DNA and RNA methylations, specifically 5-methylcytosine, 5-hydroxymethylcytosine, N6-methyladenine, and N6-methyladenosine.
  • It utilizes direct competitive immunoassays on magnetic beads and screen-printed carbon electrodes to ensure high sensitivity and selective measurement in under 45 minutes.
  • The platform has been validated for practical use, effectively distinguishing between cancerous cells and healthy tissues, particularly in colorectal cancer patients.

Article Abstract

This work reports the first electrochemical bioplatform developed for the multidetection of 5-methylcytosine (5-mC) and 5-hydroxymethylcytosine (5-hmC) in DNA, DNA N6-methyladenine (6mA) and RNA N6-methyladenosine (m6A) methylations at global level. Direct competitive immunoassays were implemented on the surface of magnetic beads (MBs) and optimized for the single amperometric determination of different targets varying in length, sequence and number of methylations on screen-printed carbon electrodes. After evaluating the sensitivity and selectivity of such determinations and the confirmation of no cross-reactivity, a multiplexed disposable platform allowing the simultaneous determination of the mentioned four methylation events in only 45 min has been prepared. The multiplexed bioplatform was successfully applied to the determination of m6A in cellular total RNA and of 5-mC, 5-hmC and 6mA in genomic DNA extracted from tissues. The developed bioplatform showed its usefulness to discriminate the aggressiveness of cancerous cells and between healthy and tumor tissues of colorectal cancer patients.

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Source
http://dx.doi.org/10.1016/j.aca.2021.338946DOI Listing

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