European Food Research and Technology

, Volume 243, Issue 10, pp 1739–1748 | Cite as

Dipeptidyl peptidase IV inhibitory peptides from Chlorella vulgaris: in silico gastrointestinal hydrolysis and molecular mechanism

  • Qiaosha Zhu
  • Xujun Chen
  • Junjie Wu
  • Yan Zhou
  • Yang Qian
  • Ming Fang
  • Jingli Xie
  • Dongzhi Wei
Original Paper
  • 261 Downloads

Abstract

Chlorella vulgaris: is a nutritional food with high protein content. Thus, 43 protein sequences from C. vulgaris were in silico gastrointestinal digested with the aid of BIOPEP. A peptide library of 468 di- and tri-peptides was built from the produced peptides. Six peptides, AAR, VPA, VPW, IPL, IPR, and PPL, were selected for DPP-IV inhibitory assay based on their sequence feature with Pro or Ala at the second N-terminal site. VPA, VPW, IPL, and IPR had potency of DPP-IV inhibition. VPW and IPR with the same N-terminal and second N-terminal sites as those of diprotin A (IPI) and diprotin B (VPL) achieved relative inhibitory IC50 value of 6.4 and 6.9 versus IPI. These peptides were further demonstrated gastrointestinal stable in vitro and could also inhibit the DPP-IV in mouse serum. Molecular docking illustrated the inhibitory mechanism of VPW and IPR. Both VPW and IPR binding with DPP-IV through hydrogen bonds, van Edward Mars interactions, and hydrophobic interactions. However, VPW formed more stable interaction with DPP-IV. The results suggested that C. vulgaris proteins would be a good source for DPP-IV inhibitory peptides.

Keywords

Chlorella vulgaris DPP-IV inhibitory peptides In silico hydrolysis Molecular docking 

Notes

Acknowledgements

This work was supported by the “National Natural Science Foundation of China (No. 31301413)”, “Open Funding Project of the State Key Laboratory of Bioreactor Engineering”, and “National Basic Research Program of China (No. 2012CB721103)”.

Compliance with ethical standards

Conflict of interest

The authors declare no conflict of interest.

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Copyright information

© Springer-Verlag Berlin Heidelberg 2017

Authors and Affiliations

  • Qiaosha Zhu
    • 1
  • Xujun Chen
    • 1
  • Junjie Wu
    • 1
  • Yan Zhou
    • 1
  • Yang Qian
    • 2
  • Ming Fang
    • 1
  • Jingli Xie
    • 1
    • 3
  • Dongzhi Wei
    • 1
    • 3
  1. 1.State Key Laboratory of Bioreactor Engineering, Department of Food Science and Technology, School of BiotechnologyEast China University of Science and TechnologyShanghaiPeople’s Republic of China
  2. 2.Department of Radiotherapy of Zhongshan HospitalFudan UniversityShanghaiPeople’s Republic of China
  3. 3.Shanghai Collaborative Innovation Center for Biomanufacturing (SCICB)ShanghaiPeople’s Republic of China

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