4.3 Article

The Kunitz chymotrypsin inhibitor from Erythrina velutina seeds displays activity against HeLa cells through arrest in cell cycle

期刊

3 BIOTECH
卷 12, 期 1, 页码 -

出版社

SPRINGER HEIDELBERG
DOI: 10.1007/s13205-021-03084-0

关键词

EvCI; HeLa cell; Cervical cancer; Apoptosis; Chymotrypsin inhibitor; Leguminous seeds

资金

  1. CAPES
  2. CNPq
  3. FINEP/RENORBIO

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In this study, a novel Kunitz-type peptidase inhibitor (EvCI) was purified and characterized from Erythrina velutina seeds. EvCI showed anti-proliferative effects against HeLa cells and selective inhibitory activity. The inhibitor demonstrated stability in inhibitory activity across a wide range of pH and temperature.
Y Erythrina velutina is a species of arboreal leguminous that occurs spontaneously in the northeastern states of Brazil. Leguminous seeds represent an abundant source of peptidase inhibitors, which play an important role in controlling peptidases involved in essential biological processes. The aim of this study was to purify and characterize a novel Kunitz-type peptidase inhibitor from Erythrina velutina seeds and evaluate its anti-proliferative effects against cancer cell lines. The Kunitz-type chymotrypsin inhibitor was purified from Erythrina velutina seeds (EvCI) by ammonium sulphate fractionation, trypsinand chymotrypsin-sepharose affinity chromatographies and Resource Q anion-exchange column. The purified EvCI has a molecular mass of 18 kDa with homology to a Kunitz-type inhibitor. Inhibition assays revealed that EvCI is a competitive inhibitor of chymotrypsin (with Ki of 4 x 10(-8) M), with weak inhibitory activity against human elastase and without inhibition against trypsin, elastase, bromelain or papain. In addition, the inhibitory activity of EvCI was stable over a wide range of pH and temperature. Disulfide bridges are involved in stabilization of the reactive site in EvCI, since the reduction of disulfide bridges with DTT 100 mM abolished similar to 50% of its inhibitory activity. The inhibitor exhibited selective anti-proliferative properties against HeLa cells. The incubation of EvCI with HeLa cells triggered arrest in the cell cycle, suggesting that apoptosis is the mechanism of death induced by the inhibitor. EvCI constitutes an interesting anti-carcinogenic candidate for conventional cervical cancer treatments employed currently. The EvCI cytostatic effect on Hela cells indicates a promised compound to be used as anti-carcinogenic complement for conventional cervical treatments employed currently.

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