Picois N, Boutahri Y, Milbeo P, Zanato C, Lensen N, Chaume G
Molecules. 2024; 29(6).
PMID: 38543045
PMC: 10974720.
DOI: 10.3390/molecules29061408.
Breunig S, Quijano J, Donohue C, Henrickson A, Demeler B, Ku H
ACS Chem Biol. 2023; 18(12):2574-2581.
PMID: 37960878
PMC: 10728891.
DOI: 10.1021/acschembio.3c00561.
Gueta O, Sheinenzon O, Azulay R, Shalit H, Strugach D, Hadar D
Front Bioeng Biotechnol. 2022; 10:913057.
PMID: 35711629
PMC: 9195583.
DOI: 10.3389/fbioe.2022.913057.
Pons A, Decaens J, Najjar R, Otog N, Arribat M, Jolly S
ACS Omega. 2022; 7(6):4868-4878.
PMID: 35187307
PMC: 8851640.
DOI: 10.1021/acsomega.1c05337.
Hartman M
Chembiochem. 2021; 23(1):e202100299.
PMID: 34416067
PMC: 9651912.
DOI: 10.1002/cbic.202100299.
Incorporation of proline analogs into recombinant proteins expressed in Escherichia coli.
Breunig S, Tirrell D
Methods Enzymol. 2021; 656:545-571.
PMID: 34325798
PMC: 9009304.
DOI: 10.1016/bs.mie.2021.05.008.
Polarity effects in 4-fluoro- and 4-(trifluoromethyl)prolines.
Kubyshkin V
Beilstein J Org Chem. 2020; 16:1837-1852.
PMID: 32765799
PMC: 7385359.
DOI: 10.3762/bjoc.16.151.
Conformational landscape of substituted prolines.
Ganguly H, Basu G
Biophys Rev. 2020; 12(1):25-39.
PMID: 31953795
PMC: 7040156.
DOI: 10.1007/s12551-020-00621-8.
The Distinct Conformational Landscapes of 4S-Substituted Prolines That Promote an endo Ring Pucker.
Costantini N, Ganguly H, Martin M, Wenzell N, Yap G, Zondlo N
Chemistry. 2019; 25(48):11356-11364.
PMID: 31237705
PMC: 6710147.
DOI: 10.1002/chem.201902382.
3-Fluoro-4-hydroxyprolines: Synthesis, Conformational Analysis, and Stereoselective Recognition by the VHL E3 Ubiquitin Ligase for Targeted Protein Degradation.
Testa A, Lucas X, Castro G, Chan K, Wright J, Runcie A
J Am Chem Soc. 2018; 140(29):9299-9313.
PMID: 29949369
PMC: 6430500.
DOI: 10.1021/jacs.8b05807.
Perfluoro-tert-butyl Homoserine Is a Helix-Promoting, Highly Fluorinated, NMR-Sensitive Aliphatic Amino Acid: Detection of the Estrogen Receptor·Coactivator Protein-Protein Interaction by F NMR.
Tressler C, Zondlo N
Biochemistry. 2017; 56(8):1062-1074.
PMID: 28165218
PMC: 5894335.
DOI: 10.1021/acs.biochem.6b01020.
cis-trans-Amide isomerism of the 3,4-dehydroproline residue, the 'unpuckered' proline.
Kubyshkin V, Budisa N
Beilstein J Org Chem. 2016; 12:589-93.
PMID: 27340450
PMC: 4901939.
DOI: 10.3762/bjoc.12.57.
4R- and 4S-iodophenyl hydroxyproline, 4R-pentynoyl hydroxyproline, and S-propargyl-4-thiolphenylalanine: conformationally biased and tunable amino acids for bioorthogonal reactions.
Forbes C, Pandey A, Ganguly H, Yap G, Zondlo N
Org Biomol Chem. 2016; 14(7):2327-46.
PMID: 26806113
PMC: 5824642.
DOI: 10.1039/c5ob02473k.
(2S,4R)- and (2S,4S)-perfluoro-tert-butyl 4-hydroxyproline: two conformationally distinct proline amino acids for sensitive application in 19F NMR.
Tressler C, Zondlo N
J Org Chem. 2014; 79(12):5880-6.
PMID: 24870929
PMC: 4076032.
DOI: 10.1021/jo5008674.
(2S,4R)-4-hydroxyproline(4-nitrobenzoate): strong induction of stereoelectronic effects via a readily synthesized proline derivative. Crystallographic observation of a correlation between torsion angle and bond length in a hyperconjugative....
Pandey A, Yap G, Zondlo N
J Org Chem. 2014; 79(9):4174-9.
PMID: 24720652
PMC: 4017608.
DOI: 10.1021/jo500367d.
Multiple site-selective insertions of noncanonical amino acids into sequence-repetitive polypeptides.
Wu I, Patterson M, Carpenter Desai H, Mehl R, Giorgi G, Conticello V
Chembiochem. 2013; 14(8):968-78.
PMID: 23625817
PMC: 3786561.
DOI: 10.1002/cbic.201300069.
Proline editing: a general and practical approach to the synthesis of functionally and structurally diverse peptides. Analysis of steric versus stereoelectronic effects of 4-substituted prolines on conformation within peptides.
Pandey A, Naduthambi D, Thomas K, Zondlo N
J Am Chem Soc. 2013; 135(11):4333-63.
PMID: 23402492
PMC: 4209921.
DOI: 10.1021/ja3109664.
Synthesis of 5-fluoro- and 5-hydroxymethanoprolines via lithiation of N-BOC-methanopyrrolidines. Constrained Cγ-exo and Cγ-endo Flp and Hyp conformer mimics.
Krow G, Shoulders M, Edupuganti R, Gandla D, Yu F, Sonnet P
J Org Chem. 2012; 77(12):5331-44.
PMID: 22607128
PMC: 3381989.
DOI: 10.1021/jo300700a.
Variation of the intercalating proline in artificial peptides mimicking the DNA binding and bending IHF protein.
Scholz S, Liebler E, Eickmann B, Fritz H, Diederichsen U
Amino Acids. 2011; 43(1):289-98.
PMID: 21922266
PMC: 3374092.
DOI: 10.1007/s00726-011-1073-1.
Elastomeric polypeptide-based biomaterials.
Li L, Charati M, Kiick K
J Polym Sci A Polym Chem. 2011; 1(8):1160-1170.
PMID: 21637725
PMC: 3104281.
DOI: 10.1039/b9py00346k.
