Cooperative Intramolecular Hydrogen Bonding Strongly Enforces cis-Peptoid Folding
datasetposted on 2019-11-25, 19:05 authored by Andrew W. Wijaya, Andy I. Nguyen, Leah T. Roe, Glenn L. Butterfoss, Ryan K. Spencer, Nan K. Li, Ronald N. Zuckermann
Sequence-defined peptoids, or N-substituted glycines, are an attractive class of bioispired polymer due to their biostability and efficient synthesis. However, the de novo design of folded peptoids with precise three-dimensional structures has been hindered by limited means to deterministically control backbone conformation. Peptoid folds are generally destabilized by the cis/trans backbone-amide isomerization, and few side-chains are capable of enforcing a specific amide conformation. Here, we show that a novel class of cationic alkyl ammonium ethyl side-chains demonstrates significant enforcement of the cis-amide backbone (Kcis/trans up to 70) using an unexpected ensemble of weak intramolecular CH–O and/or NH–O hydrogen bonds between the side-chain and the backbone carbonyl moieties. These interactions are evidenced by X-ray crystallography, variable-temperature NMR spectroscopy, and DFT calculations. Moreover, these side-chains are inexpensive, structurally diverse, hydrophilic, and can be integrated into longer peptoid sequences via solid-phase synthesis. Notably, we extended these concepts to synthesize a water-soluble peptoid 10-mer that adopts one predominant fold in solution, as determined by multidimensional NMR spectroscopy. This decamer, to the best of our knowledge, is the longest linear peptoid sequence atomically characterized to retain a well-folded structure. These findings fill a critical gap in peptoid folding and should propel the development of peptoid applications in a broad range of contexts, from pharmaceutical to material sciences.
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Cooperative Intramolecular Hydrogen Bondingpeptoid sequence atomicallydeterministically control backbone conformationpeptoid applicationsbioispired polymervariable-temperature NMR spectroscopycationic alkyl ammonium ethyl side-chainswell-folded structureNHamide conformationSequence-defined peptoidsEnforces cisamide backboneCHX-ray crystallographypeptoid sequencesmaterial sciencesNMR spectroscopybackbone carbonyl moietiesDFT calculationsnovel classsolid-phase synthesispeptoid 10- merPeptoid folds