Literature DB >> 21861531

Extraordinarily robust polyproline type I peptoid helices generated via the incorporation of α-chiral aromatic N-1-naphthylethyl side chains.

Joseph R Stringer1, J Aaron Crapster, Ilia A Guzei, Helen E Blackwell.   

Abstract

Peptoids, or oligomers of N-substituted glycines, are a class of foldamers that have shown extraordinary functional potential since their inception nearly two decades ago. However, the generation of well-defined peptoid secondary structures remains a difficult task. This challenge is due, in part, to the lack of a thorough understanding of peptoid sequence-structure relationships and, consequently, an incomplete understanding of the peptoid folding process. We seek to delineate sequence-structure relationships through the systematic study of noncovalent interactions in peptoids and the design of novel amide side chains capable of such interactions. Herein, we report the synthesis and detailed structural analysis of a series of (S)-N-(1-naphthylethyl)glycine (Ns1npe) peptoid homo-oligomers by X-ray crystallography, NMR spectroscopy, and circular dichroism (CD) spectroscopy. Four of these peptoids were found to adopt well-defined structures in the solid state, with dihedral angles similar to those observed in polyproline type I (PPI) peptide helices and in peptoids with α-chiral side chains. The X-ray crystal structure of a representative Ns1npe tetramer revealed an all cis-amide helix, with approximately three residues per turn, and a helical pitch of approximately 6.0 Å. 2D-NMR analysis of the length-dependent Ns1npe series showed that these peptoids have very high overall backbone amide K(cis/trans) values in acetonitrile, indicative of conformationally homogeneous structures in solution. Additionally, CD spectroscopy studies of the Ns1npe homo-oligomers in acetonitrile and methanol revealed a striking length-dependent increase in ellipticity per amide. These Ns1npe helices represent the most robust peptoid helices to be reported, and the incorporation of (S)-N-(1-naphthylethyl)glycines provides a new approach for the generation of stable helical structure in this important class of foldamers.

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Year:  2011        PMID: 21861531      PMCID: PMC3186054          DOI: 10.1021/ja204755p

Source DB:  PubMed          Journal:  J Am Chem Soc        ISSN: 0002-7863            Impact factor:   15.419


  40 in total

1.  Peptoid oligomers with alpha-chiral, aromatic side chains: effects of chain length on secondary structure.

Authors:  C W Wu; T J Sanborn; R N Zuckermann; A E Barron
Journal:  J Am Chem Soc       Date:  2001-04-04       Impact factor: 15.419

2.  Transformation of low-affinity lead compounds into high-affinity protein capture agents.

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Journal:  Chem Biol       Date:  2004-08

3.  Construction of peptoids with all trans-amide backbones and peptoid reverse turns via the tactical incorporation of N-aryl side chains capable of hydrogen bonding.

Authors:  Joseph R Stringer; J Aaron Crapster; Ilia A Guzei; Helen E Blackwell
Journal:  J Org Chem       Date:  2010-09-17       Impact factor: 4.354

4.  Local and tunable n-->pi* interactions regulate amide isomerism in the peptoid backbone.

Authors:  Benjamin C Gorske; Brent L Bastian; Grant D Geske; Helen E Blackwell
Journal:  J Am Chem Soc       Date:  2007-07-03       Impact factor: 15.419

5.  Chiral N-substituted glycines can form stable helical conformations.

Authors:  P Armand; K Kirshenbaum; A Falicov; R L Dunbrack; K A Dill; R N Zuckermann; F E Cohen
Journal:  Fold Des       Date:  1997

6.  Hierarchical self-assembly of a biomimetic diblock copolypeptoid into homochiral superhelices.

Authors:  Hannah K Murnen; Adrianne M Rosales; Jonathan N Jaworski; Rachel A Segalman; Ronald N Zuckermann
Journal:  J Am Chem Soc       Date:  2010-10-22       Impact factor: 15.419

7.  Peptoids that mimic the structure, function, and mechanism of helical antimicrobial peptides.

Authors:  Nathaniel P Chongsiriwatana; James A Patch; Ann M Czyzewski; Michelle T Dohm; Andrey Ivankin; David Gidalevitz; Ronald N Zuckermann; Annelise E Barron
Journal:  Proc Natl Acad Sci U S A       Date:  2008-02-19       Impact factor: 11.205

8.  Discovering ligands for a microRNA precursor with peptoid microarrays.

Authors:  Sara Chirayil; Rachel Chirayil; Kevin J Luebke
Journal:  Nucleic Acids Res       Date:  2009-06-26       Impact factor: 16.971

9.  Selective toxin sequestrants for the treatment of bacterial infections.

Authors:  Levi S Simpson; Lyle Burdine; Amal K Dutta; Andrew P Feranchak; Thomas Kodadek
Journal:  J Am Chem Soc       Date:  2009-04-29       Impact factor: 15.419

10.  Structural and spectroscopic studies of peptoid oligomers with alpha-chiral aliphatic side chains.

Authors:  Cindy W Wu; Kent Kirshenbaum; Tracy J Sanborn; James A Patch; Kai Huang; Ken A Dill; Ronald N Zuckermann; Annelise E Barron
Journal:  J Am Chem Soc       Date:  2003-11-05       Impact factor: 15.419

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  30 in total

1.  De Novo Left-Handed Synthetic Peptidomimetic Foldamers.

Authors:  Fengyu She; Peng Teng; Alfredo Peguero-Tejada; Minghui Wang; Ning Ma; Timothy Odom; Mi Zhou; Erald Gjonaj; Lukasz Wojtas; Arjan van der Vaart; Jianfeng Cai
Journal:  Angew Chem Int Ed Engl       Date:  2018-07-03       Impact factor: 15.336

2.  Construction and conformational behavior of peptoids with cis-amide bond geometry: design of a peptoid with alternate φ, ψ values of inverse PP-II/PP-II and PP-I structures.

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Journal:  J Mol Model       Date:  2014-08-31       Impact factor: 1.810

3.  Macrocyclic peptoid-Peptide hybrids as inhibitors of class I histone deacetylases.

Authors:  Christian A Olsen; Ana Montero; Luke J Leman; M Reza Ghadiri
Journal:  ACS Med Chem Lett       Date:  2012-08-10       Impact factor: 4.345

4.  Fluorinated Aromatic Monomers as Building Blocks To Control α-Peptoid Conformation and Structure.

Authors:  Diana Gimenez; Guangfeng Zhou; Matthew F D Hurley; Juan A Aguilar; Vincent A Voelz; Steven L Cobb
Journal:  J Am Chem Soc       Date:  2019-02-15       Impact factor: 15.419

5.  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

6.  A reversible and highly selective inhibitor of the proteasomal ubiquitin receptor rpn13 is toxic to multiple myeloma cells.

Authors:  Darci J Trader; Scott Simanski; Thomas Kodadek
Journal:  J Am Chem Soc       Date:  2015-05-08       Impact factor: 15.419

7.  De novo structure prediction and experimental characterization of folded peptoid oligomers.

Authors:  Glenn L Butterfoss; Barney Yoo; Jonathan N Jaworski; Ilya Chorny; Ken A Dill; Ronald N Zuckermann; Richard Bonneau; Kent Kirshenbaum; Vincent A Voelz
Journal:  Proc Natl Acad Sci U S A       Date:  2012-08-20       Impact factor: 11.205

8.  Synthesis and screening of stereochemically diverse combinatorial libraries of peptide tertiary amides.

Authors:  Yu Gao; Thomas Kodadek
Journal:  Chem Biol       Date:  2013-03-21

9.  Split-and-pool synthesis and characterization of peptide tertiary amide library.

Authors:  Yu Gao; Thomas Kodadek
Journal:  J Vis Exp       Date:  2014-06-20       Impact factor: 1.355

10.  One-Bead-Two-Compound Thioether Bridged Macrocyclic γ-AApeptide Screening Library against EphA2.

Authors:  Yan Shi; Sridevi Challa; Peng Sang; Fengyu She; Chunpu Li; Geoffrey M Gray; Alekhya Nimmagadda; Peng Teng; Timothy Odom; Yan Wang; Arjan van der Vaart; Qi Li; Jianfeng Cai
Journal:  J Med Chem       Date:  2017-11-14       Impact factor: 7.446

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