Salivary Cystatins: Exploring New Post-Translational Modifications and Polymorphisms by Top-Down High-Resolution Mass Spectrometry

J Proteome Res. 2017 Nov 3;16(11):4196-4207. doi: 10.1021/acs.jproteome.7b00567.

Abstract

Cystatins are a complex family of cysteine peptidase inhibitors. In the present study, various proteoforms of cystatin A, cystatin B, cystatin S, cystatin SN, and cystatin SA were detected in the acid-soluble fraction of human saliva and characterized by a top-down HPLC-ESI-MS approach. Proteoforms of cystatin D were also detected and characterized by an integrated top-down and bottom-up strategy. The proteoforms derive from coding sequence polymorphisms and post-translational modifications, in particular, phosphorylation, N-terminal processing, and oxidation. This study increases the current knowledge of salivary cystatin proteoforms and provides the basis to evaluate possible qualitative/quantitative variations of these proteoforms in different pathological states and reveal new potential salivary biomarkers of disease. Data are available via ProteomeXchange with identifier PXD007170.

Keywords: S-type cystatins; cystatin A; cystatin B; cystatin D; human saliva; post-translational modifications; top-down high-resolution mass spectrometry.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Cysteine Proteinase Inhibitors
  • Humans
  • Mass Spectrometry
  • Phosphorylation
  • Polymorphism, Genetic*
  • Protein Processing, Post-Translational*
  • Saliva / chemistry
  • Salivary Cystatins / analysis*
  • Salivary Cystatins / metabolism

Substances

  • Cysteine Proteinase Inhibitors
  • Salivary Cystatins