A Cytokine-Inducing Hemagglutinin from Small Taros

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Abstract:

A 22.4-kDa dimeric hemagglutinin was isolated from tubers of Colocasia esculenta cv. ‘Small Taro’ by employing a purification protocol that involved ion exchange chromatography on Q-Sepharose, fast protein liquid chromatography (FPLC)-ion exchange chromatography on Mono Q, and FPLC-gel filtration on Superdex 75. The hemagglutinin was isolated from the fraction of the taro extract adsorbed on Q-Sepharose and subsequently adsorbed on Mono Q. The major absorbance peak from the Superdex 75 column constituted purified hemagglutinin. Its hemagglutinating activity could not be inhibited by simple sugars, and was stable after exposure for 30 minutes to temperatures up to 40°C and to ambient pH in the range of pH 2 to pH 13. The activity decreased progressively when the ambient temperature was raised from 40°C to 100°C. Negligible activity was detected at 100°C. The activity plummeted, with about 40% and 10% remaining, 4 minutes and 20 minutes after exposure to 100°C, respectively. About half of the activity remained at pH 0 and pH 1 whereas the activity was completely abolished at pH 14. The hemagglutinin exhibited slight anti-tumor activity toward hepatoma HepG2 cells, and weak mitogenic activity toward murine splenocytes. It induced expression of the cytokines interleukin- 1β, inteleukin-2, interferon-γ and tumor necrosis factor-α. However, it was devoid of anti-fungal activity toward a number of fungal species.





Keywords: Hemagglutinin; cytokine induction; isolation; small taro

Document Type: Research Article

DOI: http://dx.doi.org/10.2174/092986610791306742

Publication date: July 1, 2010

More about this publication?
  • Protein & Peptide Letters publishes short papers in all important aspects of protein and peptide research, including structural studies, recombinant expression, function, synthesis, enzymology, immunology, molecular modeling, drug design etc. Manuscripts must have a significant element of novelty, timeliness and urgency that merit rapid publication. Reports of crystallisation, and preliminary structure determinations of biologically important proteins are acceptable. Purely theoretical papers are also acceptable provided they provide new insight into the principles of protein/peptide structure and function.
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