1u62: Difference between revisions

From Proteopedia
Jump to navigationJump to search
← Older editNewer edit →
OCA (talk | contribs)
Bots, Bureaucrats, journal, Administrators
3,332,843 edits
No edit summary
OCA (talk | contribs)
Bots, Bureaucrats, journal, Administrators
3,332,843 edits
No edit summary
Line 1: Line 1:
[[Image:1u62.gif|left|200px]]
{{Seed}}
[[Image:1u62.png|left|200px]]


<!--
<!--
Line 9: Line 10:
{{STRUCTURE_1u62|  PDB=1u62  |  SCENE=  }}  
{{STRUCTURE_1u62|  PDB=1u62  |  SCENE=  }}  


'''NMR structure analysis of the lactoferrin-based peptide FQWQRNIRKVR in complex with lipopolysaccharide'''
===NMR structure analysis of the lactoferrin-based peptide FQWQRNIRKVR in complex with lipopolysaccharide===




==Overview==
<!--
Treatment of Gram-negative bacterial infections with antimicrobial agents can cause release of the endotoxin lipopolysaccharide (LPS), the potent initiator of sepsis, which is the major cause of mortality in intensive care units worldwide. Structural information on peptides bound to LPS can lead to the development of more effective endotoxin neutralizers. Short linear antimicrobial and endotoxin-neutralizing peptide LF11, based on the human lactoferrin, binds to LPS, inducing a peptide fold with a "T-shaped" arrangement of a hydrophobic core and two clusters of basic residues that match the distance between the two phosphate groups of LPS. Side chain arrangement of LF11 bound to LPS extends the previously proposed LPS binding pattern, emphasizing the importance of both electrostatic and hydrophobic interactions in a defined geometric arrangement. In anionic micelles, the LF11 forms amphipathic conformation with a smaller hydrophobic core than in LPS, whereas in zwitterionic micelles, the structure is even less defined. Protection of tryptophan fluorescence quenching in the order SDS&gt;LPS&gt;DPC and hydrogen exchange protection indicates the decreasing extent of insertion of the N terminus and potential role of peptide plasticity in differentiation between bacterial and eukaryotic membranes.
The line below this paragraph, {{ABSTRACT_PUBMED_15687491}}, adds the Publication Abstract to the page
(as it appears on PubMed at http://www.pubmed.gov), where 15687491 is the PubMed ID number.
-->
{{ABSTRACT_PUBMED_15687491}}


==About this Structure==
==About this Structure==
Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1U62 OCA].  
Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1U62 OCA].  


==Reference==
==Reference==
Line 27: Line 31:
[[Category: Peptide-lipopolysaccharide complex]]
[[Category: Peptide-lipopolysaccharide complex]]
[[Category: Tranferred noe]]
[[Category: Tranferred noe]]
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sat May  3 10:48:05 2008''
 
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Tue Jul 29 07:59:22 2008''

Revision as of 04:59, 29 July 2008

File:1u62.png

Template:STRUCTURE 1u62

NMR structure analysis of the lactoferrin-based peptide FQWQRNIRKVR in complex with lipopolysaccharide

Template:ABSTRACT PUBMED 15687491

About this Structure

Full experimental information is available from OCA.

Reference

Structural origin of endotoxin neutralization and antimicrobial activity of a lactoferrin-based peptide., Japelj B, Pristovsek P, Majerle A, Jerala R, J Biol Chem. 2005 Apr 29;280(17):16955-61. Epub 2005 Feb 1. PMID:15687491

Page seeded by OCA on Tue Jul 29 07:59:22 2008

Proteopedia Page Contributors and Editors (what is this?)

OCA

Retrieved from "https://proteopedia.org/index.php?title=1u62&oldid=733746"