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Clematis montana lectin, a novel mannose-binding lectin from traditional Chinese medicine with antiviral and apoptosis-inducing activities

Authors :
Peng, Hao
Lv, Hui
Wang, Ying
Liu, Yan-hong
Li, Chun-yang
Meng, Liang
Chen, Fang
Bao, Jin-ku
Source :
Peptides. Oct2009, Vol. 30 Issue 10, p1805-1815. 11p.
Publication Year :
2009

Abstract

Abstract: A novel mannose-binding lectin (designated CML) was isolated from Clematis montana Buch.-Ham stem (Ranunculaceae) using ion exchange and gel filtration chromatographies on DEAE-Sepharose and Sephacryl S-100. The purified C. montana lectin was a homodimer of 11,968.9Da subunits as determined by gel filtration and MS. The hemagglutinating activity of CML was inhibited by branched oligomannosides. The N-terminal 15-amino acid sequence of CML, DNVKYSGQVKNTGSA, has not been reported for other lectins. Also, the peptide mass fingerprinting assay confirmed that there is no match result of similar plant lectins for CML, indicating CML may be a novel plant lectin. CML showed marked antiviral activity against various viruses in cell culture. Subsequently, CML was also found to exhibit remarkable inhibitory effect on L929, HeLa, MCF7 and HepG2 cells. Furthermore, CML specially induced L929 cell apoptosis in dose-dependent manner as evidenced by MTT, fluorescent microscopy, LDH activity-based cytotoxicity assays and DNA ladder. Moreover, due to both caspase inhibitors and Western blot analyses, caspase was also found to play the important role in the potential apoptotic mechanism of CML. When the carbohydrate-binding site was fully inhibited by sugars, cytotoxicity was abruptly decreased and apoptotic phenomenon in L929 cells was not observed, suggesting a significant correlation between mannose-binding-specific activity and the antineoplastic mechanism. [Copyright &y& Elsevier]

Details

Language :
English
ISSN :
01969781
Volume :
30
Issue :
10
Database :
Academic Search Index
Journal :
Peptides
Publication Type :
Academic Journal
Accession number :
44469226
Full Text :
https://doi.org/10.1016/j.peptides.2009.06.027