Expression and purification of recombinant human α-defensins in Escherichia coli

Marzena Pazgier, Jacek Lubkowski*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

62 Scopus citations

Abstract

Different strategies have been developed to produce small antimicrobial peptides (AMPs) using recombinant techniques. Up to now, all efforts to obtain larger quantities of active recombinant human α-defensins have been only moderately successful. Here we report an effective method of biosynthesis of human α-defensins (hNP-1 to hNP-3 and hD-5 and hD-6) in the Escherichia coli. All the peptides, expressed as insoluble fusions with the peptide encoded by a portion of E. coli tryptophan operon (trp ΔLE 1413 polypeptide), were isolated from the inclusion bodies by immobilized metal affinity chromatography (IMAC) and separated from the fusion leader by chemical cleavage. Fully reduced peptides that were purified according to a straightforward protocol were subsequently folded, oxidized, and subjected to functional and structural analyses. With the exception of hD-6, all recombinant α-defensins exhibit expected anti-E. coli activity, as measured by the colony counting method. The method described in this report is a low-cost, efficient way of generating α-defensins in quantities ranging from milligrams to grams.

Original languageEnglish
Pages (from-to)1-8
Number of pages8
JournalProtein Expression and Purification
Volume49
Issue number1
DOIs
StatePublished - Sep 2006
Externally publishedYes

Keywords

  • Antibacterial activity
  • Expression
  • Fusion protein
  • Human α-defensins
  • Purification

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