Journal
PEPTIDES
Volume 30, Issue 10, Pages 1805-1815Publisher
ELSEVIER SCIENCE INC
DOI: 10.1016/j.peptides.2009.06.027
Keywords
Clematis montana lectin; Mannose-binding-specific activity; Antiviral activity; Apoptosis; Caspase
Funding
- National Natural Science Foundation of China [30270331, 30670469]
- Director Fund of State Key Laboratory of Oral Diseases (Sichuan University)
- Science and Technology Fund for Distinguished Young Scholars of Sichuan Province [06ZQ026-035]
- Key Technologies R&D Program of Sichuan Province [2006Z08-010]
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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 11,968.9 Da 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, CIVIL 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. Crown Copyright (C) 2009 Published by Elsevier Inc. All rights reserved.
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