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Improved In-gel Reductive β-Elimination for Comprehensive O-linked and Sulfo-glycomics by Mass Spectrometry
Published on: November 20, 2014
Mucopolysaccharide from cuttlefish: Purification, chemical characterization and bioactive potential
Palaniappan Seedevi1, Meivelu Moovendhan1, Shanmugam Vairamani1
1Centre of Advanced Study in Marine Biology, Faculty of Marine Sciences, Annamalai University, Parangipettai 608 502, Tamil Nadu, India.
Sulfated glycosaminoglycan (GAG) from S. pharonis exhibits potent anticoagulant and anticancer properties. This marine-derived GAG shows significant potential as a therapeutic agent for thrombosis and cancer treatment.
Area of Science:
- Marine Biotechnology
- Biochemistry
- Pharmacology
Background:
- Glycosaminoglycans (GAGs) are crucial biomolecules with diverse biological activities.
- Investigating novel GAG sources, like marine organisms, can yield compounds with unique therapeutic potential.
Purpose of the Study:
- To isolate and characterize sulfated glycosaminoglycan (GAG) from S. pharonis.
- To evaluate the anticoagulant and anticancer activities of the isolated sulfated GAG.
Main Methods:
- Isolation and biochemical analysis of sulfated GAG from S. pharonis.
- Structural characterization using Fourier Transform Infrared (FT-IR) and NMR Spectroscopy.
- Assessment of anticoagulant activity via Activated Partial Thromboplastin Time (APTT) and Prothrombin Time (PT) assays.
- Evaluation of cytotoxic and anticancer effects on Vero and HeLa cell lines, respectively.
Main Results:
- Isolated sulfated GAG contained 62.4% carbohydrate and 3.9% protein, with a molecular weight of 27 kDa.
- The compound demonstrated significant anticoagulant activity (APTT: 91 IU, PT: 39.55 IU at 25μg/ml).
- Anticancer activity was observed against HeLa cells (18.65%-66.13% inhibition at 50-250μg/ml) with a CC50 of 1100μg/ml on Vero cells.
Conclusions:
- The sulfated GAG isolated from S. pharonis possesses significant anticoagulant and anticancer properties.
- This marine-derived GAG represents a promising candidate for future development as a dual-action therapeutic agent.
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