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- W2794605220 abstract "Cyclic peptides are a promising class of molecules for unique applications. Unfortunately, cyclic peptide design is severely limited by the difficulty in predicting the conformations they will adopt in solution. In this work, we use explicit-solvent molecular dynamics simulations to design well-structured cyclic peptides by studying their sequence–structure relationships. Critical to our approach is an enhanced sampling method that exploits the essential transitional motions of cyclic peptides to efficiently sample their conformational space. We simulated a range of cyclic pentapeptides from all-glycine to a library of cyclo-(X1X2AAA) peptides to map their conformational space and determine cooperative effects of neighboring residues. By combining the results from all cyclo-(X1X2AAA) peptides, we developed a scoring function to predict the structural preferences for X1–X2 residues within cyclic pentapeptides. Using this scoring function, we designed a cyclic pentapeptide, cyclo-(GNSRV), predicted to be well structured in aqueous solution. Subsequent circular dichroism and NMR spectroscopy revealed that this cyclic pentapeptide is indeed well structured in water, with a nuclear Overhauser effect and J-coupling values consistent with the predicted structure." @default.
- W2794605220 created "2018-04-06" @default.
- W2794605220 creator A5021760386 @default.
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- W2794605220 creator A5061428997 @default.
- W2794605220 date "2018-03-28" @default.
- W2794605220 modified "2023-09-27" @default.
- W2794605220 title "Designing Well-Structured Cyclic Pentapeptides Based on Sequence–Structure Relationships" @default.
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- W2794605220 doi "https://doi.org/10.1021/acs.jpcb.8b01747" @default.
- W2794605220 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/6071411" @default.
- W2794605220 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/29589926" @default.
- W2794605220 hasPublicationYear "2018" @default.
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