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Combining structural and bioactivity-based fingerprints improves prediction performance and scaffold hopping capability

This study aims at improving upon existing activity predictions methods by augmenting chemical structure fingerprints with bio-activity based fingerprints derived from high-throughput screening (HTS) data (HTSFPs) and thereby showcasing the benefits of combining different descriptor types. This type...

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Autores principales: Laufkötter, Oliver, Sturm, Noé, Bajorath, Jürgen, Chen, Hongming, Engkvist, Ola
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6686534/
https://www.ncbi.nlm.nih.gov/pubmed/31396716
http://dx.doi.org/10.1186/s13321-019-0376-1
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author Laufkötter, Oliver
Sturm, Noé
Bajorath, Jürgen
Chen, Hongming
Engkvist, Ola
author_facet Laufkötter, Oliver
Sturm, Noé
Bajorath, Jürgen
Chen, Hongming
Engkvist, Ola
author_sort Laufkötter, Oliver
collection PubMed
description This study aims at improving upon existing activity predictions methods by augmenting chemical structure fingerprints with bio-activity based fingerprints derived from high-throughput screening (HTS) data (HTSFPs) and thereby showcasing the benefits of combining different descriptor types. This type of descriptor would be applied in an iterative screening scenario for more targeted compound set selection. The HTSFPs were generated from HTS data obtained from PubChem and combined with an ECFP4 structural fingerprint. The bioactivity-structure hybrid (BaSH) fingerprint was benchmarked against the individual ECFP4 and HTSFP fingerprints. Their performance was evaluated via retrospective analysis of a subset of the PubChem HTS data. Results showed that the BaSH fingerprint has improved predictive performance as well as scaffold hopping capability. The BaSH fingerprint identified unique compounds compared to both the ECFP4 and the HTSFP fingerprint indicating synergistic effects between the two fingerprints. A feature importance analysis showed that a small subset of the HTSFP features contribute most to the overall performance of the BaSH fingerprint. This hybrid approach allows for activity prediction of compounds with only sparse HTSFPs due to the supporting effect from the structural fingerprint. [Image: see text] ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13321-019-0376-1) contains supplementary material, which is available to authorized users.
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spelling pubmed-66865342019-08-13 Combining structural and bioactivity-based fingerprints improves prediction performance and scaffold hopping capability Laufkötter, Oliver Sturm, Noé Bajorath, Jürgen Chen, Hongming Engkvist, Ola J Cheminform Research Article This study aims at improving upon existing activity predictions methods by augmenting chemical structure fingerprints with bio-activity based fingerprints derived from high-throughput screening (HTS) data (HTSFPs) and thereby showcasing the benefits of combining different descriptor types. This type of descriptor would be applied in an iterative screening scenario for more targeted compound set selection. The HTSFPs were generated from HTS data obtained from PubChem and combined with an ECFP4 structural fingerprint. The bioactivity-structure hybrid (BaSH) fingerprint was benchmarked against the individual ECFP4 and HTSFP fingerprints. Their performance was evaluated via retrospective analysis of a subset of the PubChem HTS data. Results showed that the BaSH fingerprint has improved predictive performance as well as scaffold hopping capability. The BaSH fingerprint identified unique compounds compared to both the ECFP4 and the HTSFP fingerprint indicating synergistic effects between the two fingerprints. A feature importance analysis showed that a small subset of the HTSFP features contribute most to the overall performance of the BaSH fingerprint. This hybrid approach allows for activity prediction of compounds with only sparse HTSFPs due to the supporting effect from the structural fingerprint. [Image: see text] ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13321-019-0376-1) contains supplementary material, which is available to authorized users. Springer International Publishing 2019-08-08 /pmc/articles/PMC6686534/ /pubmed/31396716 http://dx.doi.org/10.1186/s13321-019-0376-1 Text en © The Author(s) 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Laufkötter, Oliver
Sturm, Noé
Bajorath, Jürgen
Chen, Hongming
Engkvist, Ola
Combining structural and bioactivity-based fingerprints improves prediction performance and scaffold hopping capability
title Combining structural and bioactivity-based fingerprints improves prediction performance and scaffold hopping capability
title_full Combining structural and bioactivity-based fingerprints improves prediction performance and scaffold hopping capability
title_fullStr Combining structural and bioactivity-based fingerprints improves prediction performance and scaffold hopping capability
title_full_unstemmed Combining structural and bioactivity-based fingerprints improves prediction performance and scaffold hopping capability
title_short Combining structural and bioactivity-based fingerprints improves prediction performance and scaffold hopping capability
title_sort combining structural and bioactivity-based fingerprints improves prediction performance and scaffold hopping capability
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6686534/
https://www.ncbi.nlm.nih.gov/pubmed/31396716
http://dx.doi.org/10.1186/s13321-019-0376-1
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