Quantification of Fewer than Ten Copies of a DNA Biomarker without Amplification or Labeling

J Am Chem Soc. 2016 Jun 8;138(22):7075-81. doi: 10.1021/jacs.6b02791. Epub 2016 May 26.

Abstract

Polymerase chain reaction (PCR) is a highly sensitive diagnosis technique for detection of nucleic acids and for monitoring residual disease; however, PCR can be unreliable for samples containing very few target molecules. Here, we describe a quantification method, using force-distance (FD) curve based atomic force microscopy (AFM) to detect a target DNA bound to small (1.4-1.9 μm diameter) probe DNA spots, allowing mapping of entire spots to nanometer resolution. Using a synthetic BCR-ABL fusion gene sequence target, we examined samples containing between one and 10 target copies. A high degree of correlation (r(2) = 0.994) between numbers of target copies and detected probe clusters was observed, and the approach could detect the BCR-ABL biomarker when only a single copy was present, although multiple screens were required. Our results clearly demonstrate that FD curve-based imaging is suitable for quantitative analysis of fewer than 10 copies of DNA biomarkers without amplification, modification, or labeling.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Biomarkers / analysis
  • DNA / genetics*
  • DNA Probes
  • Fusion Proteins, bcr-abl / genetics*
  • Limit of Detection
  • Microscopy, Atomic Force / methods*
  • Polymerase Chain Reaction / methods*

Substances

  • Biomarkers
  • DNA Probes
  • DNA
  • Fusion Proteins, bcr-abl