Discovery of a novel deaminated metabolite of a single-stranded oligonucleotide in vivo by mass spectrometry

Bioanalysis. 2019 Nov;11(21):1955-1965. doi: 10.4155/bio-2019-0118.

Abstract

Aim: A novel single-stranded deaminated oligonucleotide metabolite resulting from a REVERSIR™ oligonucleotide was discovered and identified in monkey liver after subcutaneous administration. Results & methodology: REVERSIR-A and its metabolites were extracted from biological matrices by solid phase extraction and analyzed using LC coupled with high-resolution MS under negative ionization mode. A novel 9-mer metabolite of REVERSIR-A, resulting from deamination of the 3' terminal 2'-O-methyl-adenosine nucleotide to 2'-O-methyl-inosine, was discovered at significant levels in monkey liver. The metabolite's identity was confirmed by LC-MS/MS. Conclusion: This report describes the first observation of a long-chain deaminated metabolite of a single-stranded REVERSIR oligonucleotide in vivo in monkey liver.

Keywords: A-to-I editing; MS; RNAi; adenosine; deaminated metabolite; deamination; inosine; metabolism; oligonucleotide; small interfering RNA.

MeSH terms

  • Animals
  • Deamination
  • Inosine / metabolism
  • Liver / metabolism
  • Macaca fascicularis
  • Mass Spectrometry / methods*
  • Oligonucleotides / metabolism*

Substances

  • Oligonucleotides
  • Inosine