Stable isotope metabolic labeling suggests differential turnover of the DPYSL protein family

Abstract

Purpose: In this work, we discuss how in vivo ¹⁵ N metabolic labeling in combination with MS simultaneously provides information on protein expression and protein turnover.

Experimental design: We metabolically labeled mice with the stable nitrogen isotope ¹⁵ N using a ¹⁵ N-enriched diet and analyzed unlabeled (¹⁴ N) versus ¹⁵ N-labeled brain tissue with LC-MS/MS. We then compared the ¹⁴ N versus ¹⁵ N peptide isotopologue clusters of ¹⁴ N and ¹⁵ N-labeled dihydropyrimidinase-related (DPYSL) proteins.

Results: We present a workflow assessing protein expression and turnover at different time points of mouse brain development. Our data demonstrate distinct protein turnover patterns of DPYSL3 and DPYSL5 compared to other quantified proteins. We report the presence of two DPYSL3 and DPYSL5 populations with different ¹⁵ N incorporation rates, indicating altered protein turnover during development.

Conclusions and clinical relevance: In vivo ¹⁵ N metabolic labeling allows the simultaneous investigation of protein expression and turnover, enabling detailed protein dynamics studies. We report for the first time protein turnover data for the DPYSL2, DPYSL3, and DPYSL5 protein family members. As DPYSL proteins have important functions for nervous system maturation, our data provide useful information on their molecular fate during brain development.

Keywords: Biomedicine; DPYSL; LC-MS/MS; Mass spectrometry; Mouse; Protein turnover; Stable isotope labeling.