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Literature DB >> 19212995

Design of peptidic foldamer helices: a stereochemical patterning approach.

István M Mándity¹, Edit Wéber, Tamás A Martinek, Gábor Olajos, Gábor K Tóth, Elemér Vass, Ferenc Fülöp.

Abstract

Assembly language: The programmed sequences of stereochemical building blocks lead to novel biomimetic helices. The rational design approach offers new possibilities for creating periodic secondary structures.

Mesh：

Substances：
Peptides

Year: 2009 PMID： 19212995 DOI： 10.1002/anie.200805095

Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN： 1433-7851 Impact factor: 15.336

Keyword Cloud
Cited

12 in total

1. Heterogeneous H-bonding in a foldamer helix.

Authors: Brian F Fisher; Li Guo; Brian S Dolinar; Ilia A Guzei; Samuel H Gellman
Journal: J Am Chem Soc Date: 2015-05-14 Impact factor: 15.419

2. Characteristic structural parameters for the γ-peptide 14-helix: importance of subunit preorganization.

Authors: Li Guo; Weicheng Zhang; Andrew G Reidenbach; Michael W Giuliano; Ilia A Guzei; Lara C Spencer; Samuel H Gellman
Journal: Angew Chem Int Ed Engl Date: 2011-05-12 Impact factor: 15.336

3. Right-Handed Helical Foldamers Consisting of De Novo d-AApeptides.

Authors: Peng Teng; Ning Ma; Darrell Cole Cerrato; Fengyu She; Timothy Odom; Xiang Wang; Li-June Ming; Arjan van der Vaart; Lukasz Wojtas; Hai Xu; Jianfeng Cai
Journal: J Am Chem Soc Date: 2017-05-16 Impact factor: 15.419

4. Helix formation in preorganized beta/gamma-peptide foldamers: hydrogen-bond analogy to the alpha-helix without alpha-amino acid residues.

Authors: Li Guo; Aaron M Almeida; Weicheng Zhang; Andrew G Reidenbach; Soo Hyuk Choi; Ilia A Guzei; Samuel H Gellman
Journal: J Am Chem Soc Date: 2010-06-16 Impact factor: 15.419

5. Evaluation of a cyclopentane-based γ-amino acid for the ability to promote α/γ-peptide secondary structure.

Authors: Michael W Giuliano; Stacy J Maynard; Aaron M Almeida; Andrew G Reidenbach; Li Guo; Emily C Ulrich; Ilia A Guzei; Samuel H Gellman
Journal: J Org Chem Date: 2013-12-05 Impact factor: 4.354

6. Stereoselective synthesis of perillaldehyde-based chiral β-amino acid derivatives through conjugate addition of lithium amides.

Authors: Zsolt Szakonyi; Reijo Sillanpää; Ferenc Fülöp
Journal: Beilstein J Org Chem Date: 2014-11-21 Impact factor: 2.883

Design of peptidic foldamer helices: a stereochemical patterning approach.

1. Heterogeneous H-bonding in a foldamer helix.

2. Characteristic structural parameters for the γ-peptide 14-helix: importance of subunit preorganization.

3. Right-Handed Helical Foldamers Consisting of De Novo d-AApeptides.

4. Helix formation in preorganized beta/gamma-peptide foldamers: hydrogen-bond analogy to the alpha-helix without alpha-amino acid residues.

5. Evaluation of a cyclopentane-based γ-amino acid for the ability to promote α/γ-peptide secondary structure.

6. Stereoselective synthesis of perillaldehyde-based chiral β-amino acid derivatives through conjugate addition of lithium amides.

7. Homochirality of β-Peptides: A Significant Biomimetic Property of Unnatural Systems.

8. Efficient Enzymatic Routes for the Synthesis of New Eight-membered Cyclic β-Amino Acid and β-Lactam Enantiomers.

9. Proteomimetic surface fragments distinguish targets by function.

10. A foldamer-dendrimer conjugate neutralizes synaptotoxic β-amyloid oligomers.