Please use this identifier to cite or link to this item:
|Title:||Sequence and structural diversity in endotoxin-binding dodecapeptides|
Surface plasmon resonance (SPR)
|Citation:||Zhu, Y., Ding, J.L., Ho, B. (2003). Sequence and structural diversity in endotoxin-binding dodecapeptides. Biochimica et Biophysica Acta - Biomembranes 1611 (1-2) : 234-242. ScholarBank@NUS Repository.|
|Abstract:||For the study of sequence or structure requirement of short peptides for endotoxin binding, and to search for potential endotoxin antagonists, biopanning was carried out on a phage-displayed random dodecapeptide library against immobilized lipopolysaccharide (LPS) or lipid A (LA), the core toxic portion of LPS. Specific binding of selected phage-displayed peptides to LPS/LA was confirmed by surface plasmon resonance (SPR) analysis. These peptides are rich in basic and hydrophobic amino acids, especially histidine, proline and tryptophan, highlighting apparent amphiphilicity and bacterial membrane activity. These dodecapeptide sequences have no predictable secondary structure in solution, indicating the importance of a random structure before their interaction with LPS/LA. Sequence alignment reveals various potential secondary structures with these selected peptides, which contain specific signature motifs such as b(p)hb(p)hb(p), bbbb, hhhh (b - basic, p - polar, h - hydrophobic residue), capable of binding LPS/LA. However, none of these peptides exhibit a significant calculated structural amphiphilicity while assuming a secondary structure. This study suggests that for these short dodecapeptides to bind LPS/LA, the potential for their structural adaptation is more important than an amphipathic structure. © 2003 Elsevier Science B.V. All rights reserved.|
|Source Title:||Biochimica et Biophysica Acta - Biomembranes|
|Appears in Collections:||Staff Publications|
Show full item record
Files in This Item:
There are no files associated with this item.
checked on Feb 27, 2018
WEB OF SCIENCETM
checked on Apr 23, 2018
checked on May 19, 2018
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.