Data di Pubblicazione:
2014
Citazione:
Characterization of Myriocin and some derivatives by electrospray and qtrap mass spectrometry / F.M. Rubino, P. Signorelli, J.S. Lazarevic, R. Paroni. ((Intervento presentato al 8. convegno MS-Pharmaday : Complex substances for Botanical Drugs, Herbal Medicinal Products,
Medical Devices, Medical Foods tenutosi a Sansepolcro nel 2014.
Abstract:
Myriocin (or thermocydin) (I) was isolated and identified in the 1970s from fungi such as Myriococcum albomyces.
Mass spectrometry played at the time only a limited role in the structural elucidation due to the presence in the molecule of several high polarity functional groups: three hydroxyls, one primary amine, one carboxylic acid and one ketone carbonyl group. However, electron ionization of some derivatives yielded structurally diagnostic fragments, on the basis of which the mutual connectivity of the different functional groups in the 21-carbon chain could be assigned.
Pharmacological studies on myriocin and on some synthetic analogues later unveiled its strong pharmacological activity as an immunosuppressant and as an inhibitor of sphingosine synthesis and, very recently the mechanism for the inactivation of its target, serine palmitoyl transferase, was identified at the molecular level as involving the formation of a Schiff base with the cofactor pyridoxal phosphate.
Currently ongoing studies aimed at expanding its therapeutical use for the treatment of severe diseases such as retinitis pigmentosa need a specific and sensitive analytical method based on mass spectrometry, since that recently published, which uses liquid chromatography with fluorescence detection of a derivative, may not be entirely adequate to the purpose. The characterization of underivatized myriocin with the new techniques of soft ionization and tandem mass spectrometry has not been so far carried and this limitation has hampered the setup of a suitable analytical method. We have thus studied the behaviour of myriocin and of some derivatives suitable for its analytical determination in biological samples by high-sensitivity mass spectrometry.
All spectroscopic measurements were performed by infusing 1-10 microM solutions of the compounds in the ESI source of an API 3200Qtrap instrument and recording (collisionally activated) integrated fragment ion spectra of the protonated and deprotonated precursors in the profile mode over the range of nominal (laboratory) collision energies from 5 to 50 V with the instrument’s “ramp CE” feature in the Multi Channel Analysis mode. Fragment recording was accomplished either by scanning the Q3 or operating the Q3 in the ion trap mode.
As an example, the spectrum of protonated (I) is reported. Unimolecular collisionally activated decomposition of protonated and of deprotonated myriocin performed in a triple quadrupole (Qtrap) instrument over a wide interval of collision energies (0,3-3.3 eV CoM) yields a poorly diagnostic fragmentation, mostly involving the sequential loss of small molecular units from the very polar and multiply functionalized head of the molecule and the threonine-connected head-group fragment, but little analytically useful fragmentation carrying the information on the position of the keto group, in particular for the deprotonated molecule. In the accessible domain of collision energies (0.3 to 3.2 eVCM) the multifunctional polar head of the molecules undergoes several expected fragmentation processes, both in protonated and in deprotonated molecular species, and yields low-mass fragments related to its threonine structural unit. Fragments representing the position and nature of the substituent along the hydrocarbon chain are of very low abundance and, as expected, only occur starting from relatively high collision energy (data not reported).
This unfavourable characteristics prompted to extend the study to some simple derivatives of the two most accessible functional groups in the molecule, also aimed at identifying the most useful strategy for labelling the molecule with stable isotopes to prepare an analytical internal standard with suitable characteristics for the very high sensitivi
Tipologia IRIS:
14 - Intervento a convegno non pubblicato
Keywords:
Collision induced dissociation ; Energy-resolved mass spectrometry ; Linear Quadrupole ion trap ; Retinite pigmentosa ; Sphingosine
Elenco autori:
F.M. Rubino, P. Signorelli, J.S. Lazarevic, R. Paroni
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