Direct and nondestructive verification of PNA immobilization using click chemistry

Biochem Biophys Res Commun. 2008 Nov 28;376(4):633-6. doi: 10.1016/j.bbrc.2008.08.147. Epub 2008 Sep 7.

Abstract

The fluorogenic 1,3-Huisgen dipolar cycloaddition reaction was used as part of a novel immobilization strategy of PNA capture probes on a microarray. By using this click chemistry, azidocoumarin-anchored PNA probes were immobilized on phenyl acetylene-modified glass slides with the simultaneous generation of the fluorescent triazolylcoumarin moiety. Since the emitting moieties are generated in the immobilization reaction itself, fluorescent signals can be used to directly monitor the integrity of immobilization in a nondestructive manner. By using this strategy, PNA microarrays were prepared and successfully employed to perform microarray-based diagnosis of selected mutations in the breast cancer susceptibility gene BRCA1.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetylene / analogs & derivatives
  • Acetylene / chemistry
  • Azides / chemistry
  • Breast Neoplasms / diagnosis
  • Breast Neoplasms / genetics
  • Coumarins / chemistry
  • DNA Mutational Analysis / methods*
  • Fluorescent Dyes / chemistry
  • Genes, BRCA1
  • Glass / chemistry
  • Humans
  • Oligonucleotide Array Sequence Analysis / methods*
  • Oligonucleotide Probes / chemistry
  • Peptide Nucleic Acids / chemistry*
  • Spectrometry, Fluorescence / methods*

Substances

  • Azides
  • Coumarins
  • Fluorescent Dyes
  • Oligonucleotide Probes
  • Peptide Nucleic Acids
  • phenylacetylene
  • coumarin
  • Acetylene