Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/101384
Title: Rational optimization of conformational effects induced by hydrocarbon staples in peptides and their binding interfaces
Authors: Lama, Dilraj
Lakshminarayanan, Rajamani
Lane, David P.
Brown, Christopher J.
Quah, Soo T.
Verma, Chandra S.
Beuerman, Roger W.
Keywords: DRNTU::Science::Biological sciences
Issue Date: 2013
Source: Lama, D., Quah, S. T., Verma, C. S., Lakshminarayanan, R., Beuerman, R. W., Lane, D. P., et al. (2013). Rational optimization of conformational effects induced by hydrocarbon staples in peptides and their binding interfaces. Scientific reports, 3, 1-10.
Series/Report no.: Scientific reports
Abstract: eIF4E is frequently over-expressed in different cancers and causes increased translation of oncogenic proteins via deregulated cap-dependent translation. Inhibitors of the eIF4E:eIF4G interactions represent an approach that would normalize cap-dependent translation. Stapled peptides represent an emerging class of therapeutics that can target protein: protein interactions. We present here molecular dynamics simulations for a set of rationally designed stapled peptides in solution and in complex with eIF4E, supported with biophysical and crystallographic data. Clustering of the simulated structures revealed the favoured conformational states of the stapled peptides in their bound or free forms in solution. Identifying these populations has allowed us to design peptides with improved affinities by introducing mutations into the peptide sequence to alter their conformational distributions. These studies emphasise the effects that engineered mutations have on the conformations of free and bound peptides, and illustrate that both states must be considered in efforts to attain high affinity binding.
URI: https://hdl.handle.net/10356/101384
http://hdl.handle.net/10220/18637
ISSN: 2045-2322
DOI: 10.1038/srep03451
Rights: © 2013 The Author(s). This paper was published in Scientific Reports and is made available as an electronic reprint (preprint) with permission of the Author(s). The paper can be found at the following official DOI: [http://dx.doi.org/10.1038/srep03451]. One print or electronic copy may be made for personal use only. Systematic or multiple reproduction, distribution to multiple locations via electronic or other means, duplication of any material in this paper for a fee or for commercial purposes, or modification of the content of the paper is prohibited and is subject to penalties under law.
Fulltext Permission: open
Fulltext Availability: With Fulltext
Appears in Collections:SBS Journal Articles

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