Literature DB >> 15154847

Recombinant antimicrobial peptides efficiently produced using novel cloning and purification processes.

Luba Metlitskaia1, Jennifer E Cabralda, Dinar Suleman, Cynthia Kerry, Jacquelyn Brinkman, Daniel Bartfeld, M Marta Guarna.   

Abstract

Endogenous antimicrobial peptides are ubiquitous components of animal and plant host defences. These peptides, usually cationic and amphipathic, kill target cells rapidly and are efficacious against antibiotic-resistant and clinically relevant pathogens. A practical challenge in the development of cationic peptides as therapeutics is to meet the production requirements for large quantities of highly purified drug substance at competitive costs. While chemical peptide synthesis can be used to manufacture cationic peptides, we have developed cost-effective methods for recombinant production by expressing fusion proteins comprised of multiple copies of the peptides. The fusion proteins accumulate in Escherichia coli inclusion bodies and constitute over 50% of the total cellular proteins. Active antimicrobial peptides are released by chemical reagents and purified by chromatography, combining both standard and novel approaches. Challenges of industrial-scale manufacturing of therapeutics were considered in the development of this process.

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Year:  2004        PMID: 15154847     DOI: 10.1042/BA20030100

Source DB:  PubMed          Journal:  Biotechnol Appl Biochem        ISSN: 0885-4513            Impact factor:   2.431


  1 in total

1.  Length effects in antimicrobial peptides of the (RW)n series.

Authors:  Zhigang Liu; Anna Brady; Anne Young; Brian Rasimick; Kang Chen; Chunhui Zhou; Neville R Kallenbach
Journal:  Antimicrob Agents Chemother       Date:  2006-12-04       Impact factor: 5.191

  1 in total

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