Structural elucidation of foldamers with no long range conformational order.
暂无分享,去创建一个
I. Huc | H. Masu | V. Maurizot | A. Tanatani | Mayumi Kudo | Aya Tanatani
[1] Jihyun Shim,et al. Structural characterization of α/β-peptides having alternating residues: X-ray structures of the 11/9-helix from crystals of racemic mixtures. , 2013, Angewandte Chemie.
[2] I. Huc,et al. Structure elucidation of host-guest complexes of tartaric and malic acids by quasi-racemic crystallography. , 2013, Angewandte Chemie.
[3] Joseph R. Gord,et al. Role of ring-constrained γ-amino acid residues in α/γ-peptide folding: single-conformation UV and IR spectroscopy. , 2013, The journal of physical chemistry. A.
[4] S. Gellman,et al. Evidence for phenylalanine zipper-mediated dimerization in the X-ray crystal structure of a magainin 2 analogue. , 2013, Journal of the American Chemical Society.
[5] Veera V. E. Ramesh,et al. Switching the H-bonding network of a foldamer by modulating the backbone chirality and constitutional ratio of amino acids. , 2013, Organic & biomolecular chemistry.
[6] P. R. Rajamohanan,et al. A synthetic zipper peptide motif orchestrated via co-operative interplay of hydrogen bonding, aromatic stacking, and backbone chirality. , 2013, Journal of the American Chemical Society.
[7] G. Guichard,et al. Influence of achiral units with gem-dimethyl substituents on the helical character of aliphatic oligourea foldamers. , 2013, Chemical communications.
[8] I. Huc,et al. Folding of a linear array of α-amino acids within a helical aromatic oligoamide frame. , 2013, Journal of the American Chemical Society.
[9] H. Blackwell,et al. A peptoid ribbon secondary structure. , 2013, Angewandte Chemie.
[10] M. Laguerre,et al. Controlling helix formation in the γ-peptide superfamily: heterogeneous foldamers with urea/amide and urea/carbamate backbones. , 2013, Angewandte Chemie.
[11] Ting Qi,et al. Large-scale and chromatography-free synthesis of an octameric quinoline-based aromatic amide helical foldamer , 2013, Nature Protocols.
[12] G. V. Kolesnikov,et al. Templating irreversible covalent macrocyclization by using anions. , 2013, Chemistry.
[13] Jonas S. Laursen,et al. Cis-trans amide bond rotamers in β-peptoids and peptoids: evaluation of stereoelectronic effects in backbone and side chains. , 2013, Journal of the American Chemical Society.
[14] J. Leger,et al. Assessing the folding propensity of aliphatic units within helical aromatic oligoamide foldamers , 2012 .
[15] M. Takafuji,et al. Solvent dependence of helix stability in aromatic oligoamide foldamers. , 2012, Chemical communications.
[16] C. Caumes,et al. The click triazolium peptoid side chain: a strong cis-amide inducer enabling chemical diversity. , 2012, Journal of the American Chemical Society.
[17] F. Fülöp,et al. Peptidic foldamers: ramping up diversity. , 2012, Chemical Society reviews.
[18] G. Sanjayan,et al. Diversifying the structural architecture of synthetic oligomers: the hetero foldamer approach. , 2011, Chemical communications.
[19] Ilia A Guzei,et al. Extraordinarily robust polyproline type I peptoid helices generated via the incorporation of α-chiral aromatic N-1-naphthylethyl side chains. , 2011, Journal of the American Chemical Society.
[20] Hua Jiang,et al. Template-induced screw motions within an aromatic amide foldamer double helix. , 2011, Angewandte Chemie.
[21] P. Balaram,et al. Structural chemistry of peptides containing backbone expanded amino acid residues: conformational features of β, γ, and hybrid peptides. , 2011, Chemical reviews.
[22] B. Baptiste,et al. Solid phase synthesis of aromatic oligoamides: application to helical water-soluble foldamers. , 2010, The Journal of organic chemistry.
[23] S. Gellman,et al. Helix formation in preorganized beta/gamma-peptide foldamers: hydrogen-bond analogy to the alpha-helix without alpha-amino acid residues. , 2010, Journal of the American Chemical Society.
[24] Guy Duportail,et al. Consequences of isostructural main-chain modifications for the design of antimicrobial foldamers: helical mimics of host-defense peptides based on a heterogeneous amide/urea backbone. , 2010, Angewandte Chemie.
[25] Bradley D. Smith,et al. Discovery and early development of squaraine rotaxanes. , 2009, Chemical communications.
[26] F. Fülöp,et al. Stabilisation of Peptide foldamers in an aqueous medium by incorporation of azapeptide building blocks. , 2009, Chemistry.
[27] M. Delville,et al. Nanosized hybrid oligoamide foldamers: aromatic templates for the folding of multiple aliphatic units. , 2009, Journal of the American Chemical Society.
[28] Bradley D. Smith,et al. Cycloaddition to an anthracene-derived macrocyclic receptor with supramolecular control of regioselectivity. , 2009, Chemical communications.
[29] I. Mándity,et al. Design of peptidic foldamer helices: a stereochemical patterning approach. , 2009, Angewandte Chemie.
[30] V. Puranik,et al. Sequence-specific unusual (1-->2)-type helical turns in alpha/beta-hybrid peptides. , 2008, Journal of the American Chemical Society.
[31] Richard Bonneau,et al. Oligo(N-aryl glycines): a new twist on structured peptoids. , 2008, Journal of the American Chemical Society.
[32] M. Takafuji,et al. Kinetics of helix-handedness inversion: folding and unfolding in aromatic amide oligomers. , 2008, Chemphyschem : a European journal of chemical physics and physical chemistry.
[33] W Seth Horne,et al. Foldamers with heterogeneous backbones. , 2008, Accounts of chemical research.
[34] S. Gellman,et al. Single-conformation ultraviolet and infrared spectroscopy of model synthetic foldamers: beta-peptides Ac-beta3-hPhe-beta3-hAla-NHMe and Ac-beta3-hAla-beta3-hPhe-NHMe. , 2008, Journal of the American Chemical Society.
[35] J. Leger,et al. The herringbone helix: a noncanonical folding in aromatic-aliphatic peptides. , 2007, Journal of the American Chemical Society.
[36] S. Ravindranathan,et al. Conformationally constrained aliphatic-aromatic amino-acid-conjugated hybrid foldamers with periodic beta-turn motifs. , 2007, The Journal of organic chemistry.
[37] Jeffrey S. Moore,et al. The chain-length dependence test. , 2006, Accounts of chemical research.
[38] M. Laguerre,et al. Solution structure of quinoline- and pyridine-derived oligoamide foldamers. , 2005, Chemistry.
[39] S. Gellman,et al. Two Helical Conformations from a Single Foldamer Backbone: “Split Personality” in Short α/β‐Peptides , 2004 .
[40] B. Jagannadh,et al. Robust mixed 10/12 helices promoted by "alternating chirality" in a new family of C-linked carbo-beta-peptides. , 2003, Journal of the American Chemical Society.
[41] K. Dill,et al. Structural and spectroscopic studies of peptoid oligomers with alpha-chiral aliphatic side chains. , 2003, Journal of the American Chemical Society.
[42] J. Leger,et al. Aromatic δ-Peptides , 2003 .
[43] J. Snyder,et al. On the Stability of a Single-Turn α-Helix: The Single versus Multiconformation Problem , 2003 .
[44] Xavier Daura,et al. Can One Derive the Conformational Preference of a β-Peptide from Its CD Spectrum? , 2002 .
[45] J. Lehn,et al. Helical molecular programming: folding of oligopyridine-dicarboxamides into molecular single helices. , 2001, Chemistry.
[46] Bing Gong,et al. A new class of folding oligomers: Crescent oligoamides [4] , 2000 .
[47] J S Moore,et al. Solvophobically driven folding of nonbiological oligomers. , 1997, Science.
[48] Samuel H. Gellman,et al. β-Peptide Foldamers: Robust Helix Formation in a New Family of β-Amino Acid Oligomers , 1996 .
[49] A. Lombardi,et al. Discovering protein secondary structures: Classification and description of isolated α‐turns , 1996 .
[50] J. Wright,et al. Multiconformational analysis of solution NOE data for the Ac-(L)proline-(D)alanine-NHMe dipeptide in a nonprotic solvent. , 1995, Journal of magnetic resonance. Series B.
[51] Garry S. Hanan,et al. Molecular helicity: a general approach for helicity induction in a polyheterocyclic molecular strand , 1995 .