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Molecular Design Learned from the Natural Product Porphyra-334: Molecular Generation via Chemical Variational Autoencoder versus Database Mining via Similarity Search, A Comparative Study
[Image: see text] A comparative study is presented. The method via chemical variational autoencoder (VAE) and the method via similarity search are compared, focusing on their generation ability for new functional molecular design. Focusing on the natural porphyra-334 as a model molecule, we generate...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8928499/ https://www.ncbi.nlm.nih.gov/pubmed/35309498 http://dx.doi.org/10.1021/acsomega.1c06453 |
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author | Harada, Yuki Hatakeyama, Makoto Maeda, Shuichi Gao, Qi Koizumi, Kenichi Sakamoto, Yuki Ono, Yuuki Nakamura, Shinichiro |
author_facet | Harada, Yuki Hatakeyama, Makoto Maeda, Shuichi Gao, Qi Koizumi, Kenichi Sakamoto, Yuki Ono, Yuuki Nakamura, Shinichiro |
author_sort | Harada, Yuki |
collection | PubMed |
description | [Image: see text] A comparative study is presented. The method via chemical variational autoencoder (VAE) and the method via similarity search are compared, focusing on their generation ability for new functional molecular design. Focusing on the natural porphyra-334 as a model molecule, we generated three groups: molecules of mycosporine-like amino acids (MAAs) as seeds (G(SEEDS)), molecules generated via chemical VAE (G(VAE)) and molecules gathered via similarity search (G(SIM)). The number of molecules that satisfy the condition for the light absorption ability of porphyra-334 in G(SEEDS), G(VAE), and G(SIM) are 52, 138, and 6, respectively. The method via chemical VAE shows a promising potential for future molecular design. By using quantum chemistry wave function properties for chemical VAE, we find new molecules that are comparable to porphyra-334, including some with unexpected geometries. At the end, we show a group of molecules found with this method. |
format | Online Article Text |
id | pubmed-8928499 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-89284992022-03-18 Molecular Design Learned from the Natural Product Porphyra-334: Molecular Generation via Chemical Variational Autoencoder versus Database Mining via Similarity Search, A Comparative Study Harada, Yuki Hatakeyama, Makoto Maeda, Shuichi Gao, Qi Koizumi, Kenichi Sakamoto, Yuki Ono, Yuuki Nakamura, Shinichiro ACS Omega [Image: see text] A comparative study is presented. The method via chemical variational autoencoder (VAE) and the method via similarity search are compared, focusing on their generation ability for new functional molecular design. Focusing on the natural porphyra-334 as a model molecule, we generated three groups: molecules of mycosporine-like amino acids (MAAs) as seeds (G(SEEDS)), molecules generated via chemical VAE (G(VAE)) and molecules gathered via similarity search (G(SIM)). The number of molecules that satisfy the condition for the light absorption ability of porphyra-334 in G(SEEDS), G(VAE), and G(SIM) are 52, 138, and 6, respectively. The method via chemical VAE shows a promising potential for future molecular design. By using quantum chemistry wave function properties for chemical VAE, we find new molecules that are comparable to porphyra-334, including some with unexpected geometries. At the end, we show a group of molecules found with this method. American Chemical Society 2022-03-02 /pmc/articles/PMC8928499/ /pubmed/35309498 http://dx.doi.org/10.1021/acsomega.1c06453 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Harada, Yuki Hatakeyama, Makoto Maeda, Shuichi Gao, Qi Koizumi, Kenichi Sakamoto, Yuki Ono, Yuuki Nakamura, Shinichiro Molecular Design Learned from the Natural Product Porphyra-334: Molecular Generation via Chemical Variational Autoencoder versus Database Mining via Similarity Search, A Comparative Study |
title | Molecular Design Learned from the Natural Product
Porphyra-334: Molecular Generation via Chemical Variational Autoencoder
versus Database Mining via Similarity Search, A Comparative Study |
title_full | Molecular Design Learned from the Natural Product
Porphyra-334: Molecular Generation via Chemical Variational Autoencoder
versus Database Mining via Similarity Search, A Comparative Study |
title_fullStr | Molecular Design Learned from the Natural Product
Porphyra-334: Molecular Generation via Chemical Variational Autoencoder
versus Database Mining via Similarity Search, A Comparative Study |
title_full_unstemmed | Molecular Design Learned from the Natural Product
Porphyra-334: Molecular Generation via Chemical Variational Autoencoder
versus Database Mining via Similarity Search, A Comparative Study |
title_short | Molecular Design Learned from the Natural Product
Porphyra-334: Molecular Generation via Chemical Variational Autoencoder
versus Database Mining via Similarity Search, A Comparative Study |
title_sort | molecular design learned from the natural product
porphyra-334: molecular generation via chemical variational autoencoder
versus database mining via similarity search, a comparative study |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8928499/ https://www.ncbi.nlm.nih.gov/pubmed/35309498 http://dx.doi.org/10.1021/acsomega.1c06453 |
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