Optimization of protein extraction and two-dimensional gel electrophoresis profiles for the identification of Cordyceps sinensis and other similar species

PLoS One. 2018 Aug 22;13(8):e0202779. doi: 10.1371/journal.pone.0202779. eCollection 2018.

Abstract

Given that Chinese materia medica (CMM) is expensive and rare, people take tremendous risk to adulterate and falsify Cordyceps sinensis with counterfeit species with similar morphological features. It is thus essential to develop new methods to identify the authenticity of Cordyceps sinensis. It is hypothesized in this study that Cordyceps sinensis possesses certain protein biomarkers distinct from its counterfeits, which can be identified by proteomic technologies for authentication purposes. This is the first study that aims to optimize the conditions for extracting proteins from Cordyceps sinensis, a hybrid of fungal-animal CMM, and to compare the two-dimensional gel electrophoresis (2-DE) profiles between different Cordyceps species. Two different protein extraction buffer systems, namely, phenol/sodium dodecyl sulfate (SDS) buffer or lysis buffer, were evaluated, where the preparation using lysis buffer yielded better protein content. The results also showed that extraction with lysis buffer without pre- or post-washing of samples was the most effective protocol, with over 220% of protein yield and 819 protein spots detected on a 2-DE gel. Moreover, the results demonstrated that Cordyceps sinensis possesses protein biomarkers distinct from its counterfeits, and these biomarkers are not source- or origin-dependent, strongly supporting the feasibility of using identified biomarkers as indicators for authentication of Cordyceps species. The findings of this study warrant further investigations on the structural identification of protein biomarkers of Cordyceps species.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Biomarkers / analysis
  • Cordyceps / classification*
  • Cordyceps / isolation & purification
  • Cordyceps / metabolism
  • Drug Contamination
  • Electrophoresis, Gel, Two-Dimensional
  • Fungal Proteins / analysis*
  • Medicine, Chinese Traditional / standards
  • Proteomics / methods*

Substances

  • Biomarkers
  • Fungal Proteins

Grants and funding

The funding institution is Faculty Development Scheme of the Hong Kong Research Grant Council (RGC).The grant number is UGC/FDS16/P02/14. ETPS received the funding. (https://www.ugc.edu.hk/eng/rgc/index.html) The funder had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.