3D Structure, Dynamics, and Activity of Synthetic Analog of the Peptaibiotic Trichodecenin I. Issue 5 (17th May 2013)
- Record Type:
- Journal Article
- Title:
- 3D Structure, Dynamics, and Activity of Synthetic Analog of the Peptaibiotic Trichodecenin I. Issue 5 (17th May 2013)
- Main Title:
- 3D Structure, Dynamics, and Activity of Synthetic Analog of the Peptaibiotic Trichodecenin I
- Authors:
- Gatto, Emanuela
Bocchinfuso, Gianfranco
Palleschi, Antonio
Oncea, Simona
De Zotti, Marta
Formaggio, Fernando
Toniolo, Claudio
Venanzi, Mariano - Abstract:
- <abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <p>In this contribution, we report on the conformational preferences of synthetic analogs of the antimicrobial peptide trichodecenin I in solution. This 6‐amino acid residue long peptide is characterized by a single, strongly helicogenic Aib residue in the central part of the sequence and is rich in the conformationally mobile Gly residues. It has been reported that, in CHCl<sub>3</sub> solution and in the crystal state, this peptaibiotic adopts a non‐helical, multiple <italic>β</italic>‐turn conformation, whereas a <italic>3</italic><sub>10</sub>/<italic>α</italic>‐helical structure was obtained from an X‐ray diffraction study on a trichodecenin I analog (TDT4W6) containing the fluorescent Trp residue in position 6 (replacing Ile) and an equally helicogenic TOAC residue in position 4 (replacing Aib). In this work, we applied spectroscopic techniques and molecular‐dynamics calculations, in particular, on the fluorescent TDT4W6 trichodecenin I analog with the aim at investigating its 3<sc>D</sc>‐structural and dynamical features in solution. Our results revealed that TDT4W6 can be described by an ensemble of conformers quickly interconverting in the nanosecond time scale. The most populated cluster has a conformation similar to the NMR structure of native trichodecenin I in CHCl<sub>3</sub>. However, also helical‐like conformers are present, even if poorly populated and less stable under the analytical<abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <p>In this contribution, we report on the conformational preferences of synthetic analogs of the antimicrobial peptide trichodecenin I in solution. This 6‐amino acid residue long peptide is characterized by a single, strongly helicogenic Aib residue in the central part of the sequence and is rich in the conformationally mobile Gly residues. It has been reported that, in CHCl<sub>3</sub> solution and in the crystal state, this peptaibiotic adopts a non‐helical, multiple <italic>β</italic>‐turn conformation, whereas a <italic>3</italic><sub>10</sub>/<italic>α</italic>‐helical structure was obtained from an X‐ray diffraction study on a trichodecenin I analog (TDT4W6) containing the fluorescent Trp residue in position 6 (replacing Ile) and an equally helicogenic TOAC residue in position 4 (replacing Aib). In this work, we applied spectroscopic techniques and molecular‐dynamics calculations, in particular, on the fluorescent TDT4W6 trichodecenin I analog with the aim at investigating its 3<sc>D</sc>‐structural and dynamical features in solution. Our results revealed that TDT4W6 can be described by an ensemble of conformers quickly interconverting in the nanosecond time scale. The most populated cluster has a conformation similar to the NMR structure of native trichodecenin I in CHCl<sub>3</sub>. However, also helical‐like conformers are present, even if poorly populated and less stable under the analytical conditions.</p> </abstract> … (more)
- Is Part Of:
- Chemistry & biodiversity. Volume 10:Issue 5(2013:May)
- Journal:
- Chemistry & biodiversity
- Issue:
- Volume 10:Issue 5(2013:May)
- Issue Display:
- Volume 10, Issue 5 (2013)
- Year:
- 2013
- Volume:
- 10
- Issue:
- 5
- Issue Sort Value:
- 2013-0010-0005-0000
- Page Start:
- 887
- Page End:
- 903
- Publication Date:
- 2013-05-17
- Subjects:
- Biochemistry -- Periodicals
Molecular biology -- Periodicals
Biodiversity -- Periodicals
572 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1612-1880 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/cbdv.201200388 ↗
- Languages:
- English
- ISSNs:
- 1612-1872
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3168.887500
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 4042.xml