4.7 Article

An interferometric imaging biosensor using weighted spectrum analysis to confirm DNA monolayer films with attogram sensitivity

Journal

TALANTA
Volume 181, Issue -, Pages 224-231

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.talanta.2017.12.066

Keywords

Interferometric biosensor; Attogram sensitivity; Sub-nanoscale accuracy; Point mutation detection

Funding

  1. National Natural Science Foundation of China [81327005, 61361160418, 61575100]
  2. National Foundation of High Technology of China [2012AA020102, 2013AA041201]
  3. National Key Foundation for Exploring Scientific Instruments [2013YQ190467]
  4. Beijing Municipal Natural Science Foundation [4142025]
  5. Beijing Lab Foundation (BJLAB)
  6. Tsinghua Autonomous Research Foundation [2014Z01001]

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Interferometric imaging biosensors are powerful and convenient tools for confirming the existence of DNA monolayer films on silicon microarray platforms. However, their accuracy and sensitivity need further improvement because DNA molecules contribute to an inconspicuous interferometric signal both in thickness and size. Such weaknesses result in poor performance of these biosensors for low DNA content analyses and point mutation tests. In this paper, an interferometric imaging biosensor with weighted spectrum analysis is presented to confirm DNA monolayer films. The interferometric signal of DNA molecules can be extracted and then quantitative detection results for DNA microarrays can be reconstructed. With the proposed strategy, the relative error of thickness detection was reduced from 88.94% to merely 4.15%. The mass sensitivity per unit area of the proposed biosensor reached 20 attograms (ag). Therefore, the sample consumption per unit area of the target DNA content was only 62.5 zeptomoles (zm), with the volume of 0.25 picolitres (pL). Compared with the fluorescence resonance energy transfer (FRET), the measurement veracity of the interferometric imaging biosensor with weighted spectrum analysis is free to the changes in spotting concentration and DNA length. The detection range was more than 1 mu m. Moreover, single nucleotide mismatch could be pointed out combined with specific DNA ligation. A mutation experiment for lung cancer detection proved the high selectivity and accurate analysis capability of the presented biosensor.

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