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Peptaibols as a model for the insertions of chemical modifications.
Das, Sanjit; Ben Haj Salah, Khoubaib; Djibo, Mahamadou; Inguimbert, Nicolas.
Afiliación
  • Das S; USR 3278 CRIOBE, PSL Research University, EPHE-UPVD-CNRS, Université de Perpignan Via Domitia, Laboratoire d'Excellence CORAIL, Bâtiment T, 58 Avenue P. Alduy, 66860, Perpignan, France.
  • Ben Haj Salah K; USR 3278 CRIOBE, PSL Research University, EPHE-UPVD-CNRS, Université de Perpignan Via Domitia, Laboratoire d'Excellence CORAIL, Bâtiment T, 58 Avenue P. Alduy, 66860, Perpignan, France.
  • Djibo M; USR 3278 CRIOBE, PSL Research University, EPHE-UPVD-CNRS, Université de Perpignan Via Domitia, Laboratoire d'Excellence CORAIL, Bâtiment T, 58 Avenue P. Alduy, 66860, Perpignan, France.
  • Inguimbert N; USR 3278 CRIOBE, PSL Research University, EPHE-UPVD-CNRS, Université de Perpignan Via Domitia, Laboratoire d'Excellence CORAIL, Bâtiment T, 58 Avenue P. Alduy, 66860, Perpignan, France. Electronic address: nicolas.inguimbert@univ-perp.fr.
Arch Biochem Biophys ; 658: 16-30, 2018 11 15.
Article en En | MEDLINE | ID: mdl-30243710
ABSTRACT
Peptaibols are linear non ribosomal peptides which have been the object of intense research efforts regarding their synthesis and the elucidation of the mechanism allowing their insertion in biological membranes. Forty years after their discovery they are still considered as model compounds and suitable probes for the investigation of new approaches aiming to test the efficacy of new coupling reagents, to physically and spectroscopically investigate the way by which they interact with the lipid bilayer and to develop artificial membrane pores. The stable helical secondary structure adopted by the peptaibols turn to be an adequate platform for gaining insight on the structural modifications induced by the substitution of the amide bond by 1,2,3-triazoles, but also for monitoring the impact of newly designed α,α-dialkyl glycine with fluorinated and silylated side chains as 2-aminoisobutyric acid mimic. Peptaibols secondary structure dictated by Aib high content has inspired the development of foldamers. Challenges and investigations on the above mentioned topics are discussed in this brief review.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Peptaiboles Idioma: En Revista: Arch Biochem Biophys Año: 2018 Tipo del documento: Article País de afiliación: Francia

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Peptaiboles Idioma: En Revista: Arch Biochem Biophys Año: 2018 Tipo del documento: Article País de afiliación: Francia