We found a match
Your institution may have access to this item. Find your institution then sign in to continue.
- Title
Scalable Purification and Characterization of the Anticancer Lunasin Peptide from Soybean.
- Authors
Seber, Lauren E.; Barnett, Brian W.; McConnell, Elizabeth J.; Hume, Steven D.; Cai, Jian; Boles, Kati; Davis, Keith R.
- Abstract
Lunasin is a peptide derived from the soybean 2S albumin seed protein that has both anticancer and anti-inflammatory activities. Large-scale animal studies and human clinical trials to determine the efficacy of lunasin in vivo have been hampered by the cost of synthetic lunasin and the lack of a method for obtaining gram quantities of highly purified lunasin from plant sources. The goal of this study was to develop a large-scale method to generate highly purified lunasin from defatted soy flour. A scalable method was developed that utilizes the sequential application of anion-exchange chromatography, ultrafiltration, and reversed-phase chromatography. This method generates lunasin preparations of .99% purity with a yield of 442 mg/kg defatted soy flour. Mass spectrometry of the purified lunasin revealed that the peptide is 44 amino acids in length and represents the original published sequence of lunasin with an additional C-terminal asparagine residue. Histone-binding assays demonstrated that the biological activity of the purified lunasin was similar to that of synthetic lunasin. This study provides a robust method for purifying commercial-scale quantities of biologically-active lunasin and clearly identifies the predominant form of lunasin in soy flour. This method will greatly facilitate the development of lunasin as a potential nutraceutical or therapeutic anticancer agent.
- Subjects
SOYBEAN products; FORAGE plants; PEPTIDES; ANTINEOPLASTIC agents; PLANT proteins; ULTRAFILTRATION; IMINO acids
- Publication
PLoS ONE, 2012, Vol 7, Issue 4, p1
- ISSN
1932-6203
- Publication type
Article
- DOI
10.1371/journal.pone.0035409