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Solution structure of polytheonamide B, a highly cytotoxic nonribosomal polypeptide from marine sponge.

Authors :
Hamada T
Matsunaga S
Fujiwara M
Fujita K
Hirota H
Schmucki R
Güntert P
Fusetani N
Source :
Journal of the American Chemical Society [J Am Chem Soc] 2010 Sep 22; Vol. 132 (37), pp. 12941-5.
Publication Year :
2010

Abstract

Polytheonamide B (pTB), a highly cytotoxic polypeptide, is one of the most unusual nonribosomal peptides of sponge origin. pTB is a linear 48-residue peptide with alternating D- and L-amino acids and contains a total of eight types of nonproteinogenic amino acids. To investigate the mechanisms underlying its cytotoxic activity, we determined the three-dimensional structure of pTB by NMR spectroscopy, structure calculation, and energy minimization. pTB adopts a single right-handed β(6.3)-helical structure in a 1:1 mixture of methanol/chloroform with a length of approximately 45 A and a hydrophilic pore of ca. 4 A inner diameter. These features indicate that pTB molecules form transmembrane channels that permeate monovalent cations as gramicidin A channels do. The strong cytotoxicity of pTB can be ascribed to its ability to form single molecule channels through biological membranes.

Details

Language :
English
ISSN :
1520-5126
Volume :
132
Issue :
37
Database :
MEDLINE
Journal :
Journal of the American Chemical Society
Publication Type :
Academic Journal
Accession number :
20795624
Full Text :
https://doi.org/10.1021/ja104616z