dc.contributor.author | Kuczera, Krzysztof | |
dc.contributor.author | Szoszkiewicz, Robert | |
dc.contributor.author | He, Jinyan | |
dc.contributor.author | Jas, Gouri S. | |
dc.date.accessioned | 2021-12-22T19:57:39Z | |
dc.date.available | 2021-12-22T19:57:39Z | |
dc.date.issued | 2021-04-24 | |
dc.identifier.citation | Kuczera, K.; Szoszkiewicz, R.; He, J.; Jas, G.S. Length Dependent Folding Kinetics of Alanine-Based Helical Peptides from Optimal Dimensionality Reduction. Life 2021, 11, 385. https://doi.org/10.3390/life11050385 | en_US |
dc.identifier.uri | http://hdl.handle.net/1808/32303 | |
dc.description.abstract | We present a computer simulation study of helix folding in alanine homopeptides (ALA)n of length n = 5, 8, 15, and 21 residues. Based on multi-microsecond molecular dynamics simulations at room temperature, we found helix populations and relaxation times increasing from about 6% and ~2 ns for ALA5 to about 60% and ~500 ns for ALA21, and folding free energies decreasing linearly with the increasing number of residues. The helix folding was analyzed with the Optimal Dimensionality Reduction method, yielding coarse-grained kinetic models that provided a detailed representation of the folding process. The shorter peptides, ALA5 and ALA8, tended to convert directly from coil to helix, while ALA15 and ALA21 traveled through several intermediates. Coarse-grained aggregate states representing the helix, coil, and intermediates were heterogeneous, encompassing multiple peptide conformations. The folding involved multiple pathways and interesting intermediate states were present on the folding paths, with partially formed helices, turns, and compact coils. Statistically, helix initiation was favored at both termini, and the helix was most stable in the central region. Importantly, we found the presence of underlying universal local dynamics in helical peptides with correlated transitions for neighboring hydrogen bonds. Overall, the structural and dynamical parameters extracted from the trajectories are in good agreement with experimental observables, providing microscopic insights into the complex helix folding kinetics. | en_US |
dc.publisher | MDPI | en_US |
dc.rights | © 2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license. | en_US |
dc.rights.uri | https://creativecommons.org/licenses/by/4.0/ | en_US |
dc.subject | Helix folding | en_US |
dc.subject | Molecular dynamics simulation | en_US |
dc.subject | Optimal dimensionality reduction | en_US |
dc.subject | Kinetic models | en_US |
dc.title | Length Dependent Folding Kinetics of Alanine-Based Helical Peptides from Optimal Dimensionality Reduction | en_US |
dc.type | Article | en_US |
kusw.kuauthor | Kuczera, Krzysztof | |
kusw.kuauthor | He, Jinyan | |
kusw.kuauthor | Jas, Gouri S. | |
kusw.kudepartment | Chemistry | en_US |
kusw.kudepartment | Molecular Biosciences | en_US |
kusw.kudepartment | Pharmaceutical Chemistry | en_US |
dc.identifier.doi | 10.3390/life11050385 | en_US |
dc.identifier.orcid | https://orcid.org/ 0000-0003-2358-1349 | en_US |
dc.identifier.orcid | https://orcid.org/ 0000-0002-2770-8848 | en_US |
dc.identifier.orcid | https://orcid.org/ 0000-0002-0774-012X | en_US |
kusw.oaversion | Scholarly/refereed, publisher version | en_US |
kusw.oapolicy | This item meets KU Open Access policy criteria. | en_US |
dc.identifier.pmid | PMC8170890 | en_US |
dc.rights.accessrights | openAccess | en_US |