Secondary structure of muramyl dipeptide glycoside in pristine state and immobilized on nanosilica surface

Liana R. Azizova, Tetiana V. Kulik, Borys B. Palianytsia, German M. Telbiz, Mykola T. Kartel

Research output: Contribution to journalArticlepeer-review

Abstract

Fourier transform infrared spectroscopy (FT-IR) and temperature programmed desorption mass spectrometry (TPD-MS) data of O-glycoside MDP in pristine and immobilized on silica surface states indicate that O-glycoside MDP binds to the silica surface by means of carboxylic and NH moieties of isoglutamine. Moreover, pyrolysis of O-glycoside MDP on the silica surface proceeds through formation of additional product 3-iminopyridine-2(3H)-one, which identified in mass spectra as molecular ion with m/z 108 and its fragment ions with m/z 79, 77, 51. FTIR and TPD-MS data confirm existence of a MDP first β-turn on the silica surface resulting from the formation of a hydrogen bond between the NAc carbonyl and the L-Ala NH for MDP and its analogs, as reported previously.

Original languageEnglish
Article number127724
JournalColloids and Surfaces A: Physicochemical and Engineering Aspects
Volume631
DOIs
Publication statusPublished - 20 Dec 2021
Externally publishedYes

Keywords

  • Adjuvants
  • Fourier transform infrared spectroscopy (FT-IR)
  • Fumed silica
  • Immunostimulatory agents
  • Muramyl dipeptide
  • Pyrolysis
  • Temperature programmed desorption mass spectrometry (TPD-MS)
  • β-turn

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