Literature DB >> 8055943

Antibacterial peptides and mitochondrial presequences affect mitochondrial coupling, respiration and protein import.

M Hugosson1, D Andreu, H G Boman, E Glaser.   

Abstract

Cecropins A and P1, antibacterial peptides from insects and from pig and some related peptides released respiratory control, inhibited protein import and at higher concentrations also inhibited respiration. However, PR-39, an antibacterial peptide from pig intestine, was found to be almost inert towards mitochondria. The concentrations at which the three mitochondrial functions were effected varied for different peptides. Melittin, magainin and Cecropin-A-(1,13)-Melittin(1,13)-NH2, a hybrid between cecropin A and melittin, were most potent, while the two cecropins acted at higher concentrations. The biosynthesis of cecropin A is known and the intermediates are synthesized. We have used four peptides from this pathway to investigate their effects on coupling, respiration and protein import into mitochondria. Mature cecropin A followed by the preproprotein were most aggressive whereas the intermediates were less active or inert. The efficiency of different derivatives of cecropin A as uncouplers correlates well with their capacity to release membrane potential measured as fluorescence quenching of Rhodamine 123. Inhibition of respiration was found to be dependent on membrane potential and was most pronounced with mature cecropin A, less so with its three precursors. We also found that three peptides derived from mitochondrial presequences showed antibacterial activity. It is concluded that, there are similarities in the functions of antibacterial peptides and mitochondrial presequences, uncoupling activity in mitochondria cannot be correlated with the antibacterial activity (contrary to a previous suggestion), the processing of preprocecropin A may have evolved in such a way that there is a minimum of membrane damage from the intermediates in the pathway, and peptides produced for delivery outside of an animal have evolved to be more aggressive against mitochondria than peptides for delivery inside of the animal.

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Year:  1994        PMID: 8055943     DOI: 10.1111/j.1432-1033.1994.tb19081.x

Source DB:  PubMed          Journal:  Eur J Biochem        ISSN: 0014-2956


  21 in total

1.  Chemical cleavage of the overexpressed mitochondrial F1beta precursor with CNBr: a new strategy to construct an import-competent preprotein.

Authors:  P F Pavlov; P Moberg; X P Zhang; E Glaser
Journal:  Biochem J       Date:  1999-07-01       Impact factor: 3.857

2.  Rapid degradation of the presequence of the f1beta precursor of the ATP synthase inside mitochondria.

Authors:  A Ståhl; P F Pavlov; C Szigyarto; E Glaser
Journal:  Biochem J       Date:  2000-08-01       Impact factor: 3.857

3.  L and D presequence peptides derived from the precursor of F1beta subunit of the ATP synthase inhibit mitochondrial protein import by interaction with import machinery.

Authors:  C Sigyarto; M Hugosson; P Moberg; D Andreu; E Glaser
Journal:  Plant Mol Biol       Date:  2001-12       Impact factor: 4.076

4.  BMAP-28, an antibiotic peptide of innate immunity, induces cell death through opening of the mitochondrial permeability transition pore.

Authors:  Angela Risso; Enrico Braidot; Maria Concetta Sordano; Angelo Vianello; Francesco Macrì; Barbara Skerlavaj; Margherita Zanetti; Renato Gennaro; Paolo Bernardi
Journal:  Mol Cell Biol       Date:  2002-03       Impact factor: 4.272

Review 5.  MCC and PSC, the putative protein import channels of mitochondria.

Authors:  K W Kinnally; C Muro; M L Campo
Journal:  J Bioenerg Biomembr       Date:  2000-02       Impact factor: 2.945

6.  Mitochondrial biogenesis and function in Arabidopsis.

Authors:  A Harvey Millar; Ian D Small; David A Day; James Whelan
Journal:  Arabidopsis Book       Date:  2008-07-09

Review 7.  Mitochondrial protein import in plants. Signals, sorting, targeting, processing and regulation.

Authors:  E Glaser; S Sjöling; M Tanudji; J Whelan
Journal:  Plant Mol Biol       Date:  1998-09       Impact factor: 4.076

8.  The plasma membrane of Leishmania donovani promastigotes is the main target for CA(1-8)M(1-18), a synthetic cecropin A-melittin hybrid peptide.

Authors:  P Díaz-Achirica; J Ubach; A Guinea; D Andreu; L Rivas
Journal:  Biochem J       Date:  1998-02-15       Impact factor: 3.857

9.  Organellar oligopeptidase (OOP) provides a complementary pathway for targeting peptide degradation in mitochondria and chloroplasts.

Authors:  Beata Kmiec; Pedro F Teixeira; Ronnie P-A Berntsson; Monika W Murcha; Rui M M Branca; Jordan D Radomiljac; Jakob Regberg; Linda M Svensson; Amin Bakali; Ulo Langel; Janne Lehtiö; James Whelan; Pål Stenmark; Elzbieta Glaser
Journal:  Proc Natl Acad Sci U S A       Date:  2013-09-16       Impact factor: 11.205

10.  Oxidation and reduction of pyridine nucleotides in alamethicin-permeabilized plant mitochondria.

Authors:  Fredrik I Johansson; Agnieszka M Michalecka; Ian M Møller; Allan G Rasmusson
Journal:  Biochem J       Date:  2004-05-15       Impact factor: 3.857

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