Structural and functional studies of a phosphatidic acid-binding antifungal plant defensin MtDef4: Identification of an RGFRRR motif governing fungal cell entry

Uma Shankar Sagaram, Kaoutar El-Mounadi, Garry W. Buchko, Howard R. Berg, Jagdeep Kaur, Raghu S. Pandurangi, Thomas Smith, Dilip M. Shah

Research output: Contribution to journalArticle

68 Citations (Scopus)

Abstract

MtDef4 is a 47-amino acid cysteine-rich evolutionary conserved defensin from a model legume Medicago truncatula. It is an apoplast-localized plant defense protein that inhibits the growth of the ascomycetous fungal pathogen Fusarium graminearum in vitro at micromolar concentrations. Little is known about the mechanisms by which MtDef4 mediates its antifungal activity. In this study, we show that MtDef4 rapidly permeabilizes fungal plasma membrane and is internalized by the fungal cells where it accumulates in the cytoplasm. Furthermore, analysis of the structure of MtDef4 reveals the presence of a positively charged γ-core motif composed of β2 and β3 strands connected by a positively charged RGFRRR loop. Replacement of the RGFRRR sequence with AAAARR or RGFRAA abolishes the ability of MtDef4 to enter fungal cells, suggesting that the RGFRRR loop is a translocation signal required for the internalization of the protein. MtDef4 binds to phosphatidic acid (PA), a precursor for the biosynthesis of membrane phospholipids and a signaling lipid known to recruit cytosolic proteins to membranes. Amino acid substitutions in the RGFRRR sequence which abolish the ability of MtDef4 to enter fungal cells also impair its ability to bind PA. These findings suggest that MtDef4 is a novel antifungal plant defensin capable of entering into fungal cells and affecting intracellular targets and that these processes are mediated by the highly conserved cationic RGFRRR loop via its interaction with PA.

Original languageEnglish (US)
Article numbere82485
JournalPLoS One
Volume8
Issue number12
DOIs
StatePublished - Dec 4 2013
Externally publishedYes

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Defensins
Phosphatidic Acids
acids
Membranes
Amino Acids
Proteins
Biosynthesis
Medicago truncatula
Pathogens
cells
Cell membranes
Plant Proteins
Cysteine
proteins
Phospholipids
apoplast
Fusarium graminearum
Fusarium
amino acid substitution
Substitution reactions

ASJC Scopus subject areas

  • Agricultural and Biological Sciences(all)
  • Biochemistry, Genetics and Molecular Biology(all)
  • Medicine(all)

Cite this

Structural and functional studies of a phosphatidic acid-binding antifungal plant defensin MtDef4 : Identification of an RGFRRR motif governing fungal cell entry. / Sagaram, Uma Shankar; El-Mounadi, Kaoutar; Buchko, Garry W.; Berg, Howard R.; Kaur, Jagdeep; Pandurangi, Raghu S.; Smith, Thomas; Shah, Dilip M.

In: PLoS One, Vol. 8, No. 12, e82485, 04.12.2013.

Research output: Contribution to journalArticle

Sagaram, Uma Shankar ; El-Mounadi, Kaoutar ; Buchko, Garry W. ; Berg, Howard R. ; Kaur, Jagdeep ; Pandurangi, Raghu S. ; Smith, Thomas ; Shah, Dilip M. / Structural and functional studies of a phosphatidic acid-binding antifungal plant defensin MtDef4 : Identification of an RGFRRR motif governing fungal cell entry. In: PLoS One. 2013 ; Vol. 8, No. 12.
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