1.A cyclotide against influenza A H1N1 virus from Viola yedoensis.
Min-Zhi LIU ; Yan YANG ; Shu-Xiang ZHANG ; Liang TANG ; Hui-Min WANG ; Cheng-Juan CHEN ; Zhu-Fang SHEN ; Ke-Di CHENG ; Jian-Qiang KONG ; Wei WANG
Acta Pharmaceutica Sinica 2014;49(6):905-912
Three cyclotides were isolated from the whole plant of Viola yedoensis in this study. The two, vary peptide E and cycloviolacin Y5, were previously reported, and a novel cycloviolacin VY1 was characterized according to the interpretation of MS/MS fragmentation of peptides which were produced from the reduced and alkylated parent peptide with the digestion of Endo Lys-C, trypsin and chymotrypsin, separately. The stability of remarkable resistance to proteolytic degradation by trypsin and chymotrypsin, and that of thermal denaturation was confirmed again. Besides, the IC50 value of cycloviolacin VY1 against influenza A H1N1 virus was (2.27 +/- 0.20) microg x mL(-1). It is the first cyclotide reported with anti-influenza A H1N1 virus activity in vitro assay.
Antiviral Agents
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isolation & purification
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pharmacology
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Cyclotides
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pharmacology
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Influenza A Virus, H1N1 Subtype
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drug effects
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Tandem Mass Spectrometry
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Viola
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chemistry
2.Elucidating the structure of two cyclotides of Viola tianshanica maxim by MALDI TOF/TOF MS analysis.
Bin XIANG ; Guo-Hua DU ; Xu-Chen WANG ; Shu-Xiang ZHANG ; Xian-Yun QIN ; Jian-Qiang KONG ; Ke-Di CHENG ; Yong-Ji LI ; Wei WANG
Acta Pharmaceutica Sinica 2010;45(11):1402-1409
The cyclotides are a family of cyclic "mini" proteins that occur in Violaceae, Rubiaceae and Cucurbitaceae plant families and contain a head-to-tail cyclic backbone and a cystine knot arranged by three disulfide bonds. To study the natural cyclotides of V tianshanica, dried herb was extracted with 50% ethanol, and the concentrated aqueous extract was subjected to a solvent-solvent partitioning between water and hexane, ethyl acetate and n-butanol, separately. The n-butanol extract containing cyclotides was subjected to column chromatography over Sephadex LH-20, eluted with 30% methanol. The subfractions were directly reduced by DTT and analyzed by reverse-phase HPLC. The peaks with different retention times were shown on the profile of RP-HPLC and collected. The cyclotides were speculated based on masses range from 3 000 to 3 500 Da. The purified cyclotides were reduced with DTT, alkylated with iodoacetamide, and then were cleaved with endoproteinase Glu-C, endoproteinase Lys-C and Trypsin, separately. The digested peptides were purified on RP-HPLC and analyzed on MALDI TOF/TOF analyzer. A new cyclotide, cycloviolacin T1 and a reported cyclotide varv E were systemically determined using MALDI TOF/TOF system. So the method for the isolation and characterization of cyclotides was quickly built up in succession.
Amino Acid Sequence
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Chromatography, High Pressure Liquid
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Cyclotides
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chemistry
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isolation & purification
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Molecular Sequence Data
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Molecular Structure
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Plants, Medicinal
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chemistry
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Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization
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Tandem Mass Spectrometry
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Viola
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chemistry