1xkm

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(New page: 200px<br /><applet load="1xkm" size="450" color="white" frame="true" align="right" spinBox="true" caption="1xkm" /> '''NMR structure of antimicrobial peptide disti...)
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[[Image:1xkm.gif|left|200px]]<br /><applet load="1xkm" size="350" color="white" frame="true" align="right" spinBox="true"
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'''NMR structure of antimicrobial peptide distinctin in water'''<br />
'''NMR structure of antimicrobial peptide distinctin in water'''<br />
==Overview==
==Overview==
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Many bioactive peptides, presenting an unstructured conformation in, aqueous solution, are made resistant to degradation by posttranslational, modifications. Here, we describe how molecular oligomerization in aqueous, solution can generate a still unknown transport form for amphipathic, peptides, which is more compact and resistant to proteases than forms, related to any possible monomer. This phenomenon emerged from 3D, structure, function, and degradation properties of distinctin, a, heterodimeric antimicrobial compound consisting of two peptide chains, linked by a disulfide bond. After homodimerization in water, this peptide, exhibited a fold consisting of a symmetrical full-parallel four-helix, bundle, with a well secluded hydrophobic core and exposed basic residues., This fold significantly stabilizes distinctin against proteases compared, with other linear amphipathic peptides, without affecting its, antimicrobial, hemolytic, and ion-channel formation properties after, membrane interaction. This full-parallel helical orientation represents a, perfect compromise between formation of a stable structure in water and, requirement of a drastic structural rearrangement in membranes to elicit, antimicrobial potential. Thus, distinctin can be claimed as a prototype of, a previously unrecognized class of antimicrobial derivatives. These, results suggest a critical revision of the role of peptide oligomerization, whenever solubility or resistance to proteases is known to affect, biological properties.
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Many bioactive peptides, presenting an unstructured conformation in aqueous solution, are made resistant to degradation by posttranslational modifications. Here, we describe how molecular oligomerization in aqueous solution can generate a still unknown transport form for amphipathic peptides, which is more compact and resistant to proteases than forms related to any possible monomer. This phenomenon emerged from 3D structure, function, and degradation properties of distinctin, a heterodimeric antimicrobial compound consisting of two peptide chains linked by a disulfide bond. After homodimerization in water, this peptide exhibited a fold consisting of a symmetrical full-parallel four-helix bundle, with a well secluded hydrophobic core and exposed basic residues. This fold significantly stabilizes distinctin against proteases compared with other linear amphipathic peptides, without affecting its antimicrobial, hemolytic, and ion-channel formation properties after membrane interaction. This full-parallel helical orientation represents a perfect compromise between formation of a stable structure in water and requirement of a drastic structural rearrangement in membranes to elicit antimicrobial potential. Thus, distinctin can be claimed as a prototype of a previously unrecognized class of antimicrobial derivatives. These results suggest a critical revision of the role of peptide oligomerization whenever solubility or resistance to proteases is known to affect biological properties.
==About this Structure==
==About this Structure==
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1XKM is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/ ]. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1XKM OCA].
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1XKM is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/ ]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1XKM OCA].
==Reference==
==Reference==
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[[Category: pore-forming peptide]]
[[Category: pore-forming peptide]]
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''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Sun Nov 25 02:22:47 2007''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 15:55:45 2008''

Revision as of 13:55, 21 February 2008


1xkm

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NMR structure of antimicrobial peptide distinctin in water

Overview

Many bioactive peptides, presenting an unstructured conformation in aqueous solution, are made resistant to degradation by posttranslational modifications. Here, we describe how molecular oligomerization in aqueous solution can generate a still unknown transport form for amphipathic peptides, which is more compact and resistant to proteases than forms related to any possible monomer. This phenomenon emerged from 3D structure, function, and degradation properties of distinctin, a heterodimeric antimicrobial compound consisting of two peptide chains linked by a disulfide bond. After homodimerization in water, this peptide exhibited a fold consisting of a symmetrical full-parallel four-helix bundle, with a well secluded hydrophobic core and exposed basic residues. This fold significantly stabilizes distinctin against proteases compared with other linear amphipathic peptides, without affecting its antimicrobial, hemolytic, and ion-channel formation properties after membrane interaction. This full-parallel helical orientation represents a perfect compromise between formation of a stable structure in water and requirement of a drastic structural rearrangement in membranes to elicit antimicrobial potential. Thus, distinctin can be claimed as a prototype of a previously unrecognized class of antimicrobial derivatives. These results suggest a critical revision of the role of peptide oligomerization whenever solubility or resistance to proteases is known to affect biological properties.

About this Structure

1XKM is a Protein complex structure of sequences from [1]. Full crystallographic information is available from OCA.

Reference

A folding-dependent mechanism of antimicrobial peptide resistance to degradation unveiled by solution structure of distinctin., Raimondo D, Andreotti G, Saint N, Amodeo P, Renzone G, Sanseverino M, Zocchi I, Molle G, Motta A, Scaloni A, Proc Natl Acad Sci U S A. 2005 May 3;102(18):6309-14. Epub 2005 Apr 19. PMID:15840728

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