4.5 Article

Screening and quantification of TNF-α ligand from Angelicae Pubescentis Radix by biosensor and UPLC-MS/MS

Journal

ANALYTICAL BIOCHEMISTRY
Volume 596, Issue -, Pages -

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.ab.2020.113643

Keywords

TNF-alpha; SPR; UPLC-MS/MS; APR; Quality assessment; Chemometrics

Funding

  1. National Natural Science Foundation of China (China) [81973604, 81803690, 81703684]
  2. Special Funds from the Central Finance to Support the Development of Local Universities (China), Postgraduate Funds for Heilongjiang University of Chinese Medicine (Heilongjiang University of Chinese Medicine) [2019yjscx013]
  3. National Natural Science Foundation Matching Project (China) [2017PT01]
  4. Innovative Talents Funding of Heilongjiang University of Chinese Medicine (Heilongjiang University of Chinese Medicine) [2018RCD25]
  5. Postdoctoral Initial Fund of Heilongjiang Province (Heilongjiang, UNPYSCT) [2017219]
  6. University Nursing Program for Young Scholars with Creative Talents in Heilongjiang Province (Heilongjiang) [UNPYSCT-2017215]
  7. Natural Science Foundation of Heilongjiang Province (Heilongjiang) [H2015037]
  8. Heilongjiang University of Chinese Medicine Doctoral Innovation Foundation (Heilongjiang University of Chinese Medicine) [2013bs04]
  9. Application Technology Research and Development Projects of Harbin Technology Bureau (Harbin) [2014RFQXJ149]
  10. Heilongjiang Postdoctoral Scientific Research Developmental Fund (Heilongjiang) [LBH-Q16210, LBH-Q17161]

Ask authors/readers for more resources

The aim of this study is to establish a method for rapid screening of active ingredients targeting TNF-alpha from Chinese herbal medicines. Take Angelicae Pubescentis Radix (APR) as an example, surface plasma resonance technique was used to establish for screening small molecule inhibitors of TNF-alpha from APR extract. Then UPLC-MS/MS coupled with chemometric was used for quantitative and evaluate the differences of the candidate compounds bound to TNF-alpha in APR from different sources. In the experiment, TNF-alpha protein was fixed on the CM5 chip surface of biacore T200 biosensor by amino coupling. A series of small molecular compounds in APR were screened and six phenolic acid compounds had a strong affinity for TNF-alpha protein and could be used as TNF-alpha antagonists. In summary, the targeted drug screening method for TNF-alpha protein based on SPR technology established in this study can be used to screen anti-TNF-alpha small molecule inhibitors. UPLC-MS/MS can accurately quantify 15 active ingredients, which provides reliable experimental data and new research ideas for targeted drug research on TNF-alpha protein.

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