Issue 5, 2022

Mass spectrometry insights into interactions of selenoprotein P with auranofin and cisplatin

Abstract

The reactivity of selenoprotein P (a serum selenoprotein containing 10 selenocysteine (SeCys), 17 cysteine (Cys) and 14 histidine (His) residues) with two metallodrugs (auranofin and cisplatin) was investigated. The selenoprotein was purified from human serum by sequential affinity chromatography using immobilized metal (Co2+) affinity chromatography (IMAC) and heparine affinity, followed by solid-phase extraction preconcentration. The purified selenoprotein P was sequenced by nanoLC-MS/MS to reach a complete sequence coverage. It eluted from SEC as two major peaks likely to correspond to the glycosylated and non-glycosylated forms and a minor one, probably a truncated form. Size-exclusion chromatography with the selective Se (78Se) and metal (197Au or 195Pt) detection by ICP MS showed the co-elution of selenoprotein P forms with Au and with Pt. SEC-ICP MS of the tryptic digest showed a considerable shift of the elution of selenium towards the lower molecular masses while preserving the co-elution of selenium and the metal at some elution times. NanoHPLC – electrospray MS/MS analysis of the post-reaction mixture demonstrated the formation of peptides with the privileged binding to Cys and His residues for cisplatin and SeCys and Cys residues for auranofin.

Graphical abstract: Mass spectrometry insights into interactions of selenoprotein P with auranofin and cisplatin

Supplementary files

Article information

Article type
Paper
Submitted
16 Marts 2022
Accepted
07 Apr. 2022
First published
13 Apr. 2022

J. Anal. At. Spectrom., 2022,37, 1010-1022

Mass spectrometry insights into interactions of selenoprotein P with auranofin and cisplatin

J. Lamarche, K. Bierla, L. Ouerdane, J. Szpunar, L. Ronga and R. Lobinski, J. Anal. At. Spectrom., 2022, 37, 1010 DOI: 10.1039/D2JA00090C

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements