Cargando…
QSAR Accelerated Discovery of Potent Ice Recrystallization Inhibitors
Ice recrystallization is the main contributor to cell damage and death during the cryopreservation of cells and tissues. Over the past five years, many small carbohydrate-based molecules were identified as ice recrystallization inhibitors and several were shown to reduce cryoinjury during the cryopr...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4877635/ https://www.ncbi.nlm.nih.gov/pubmed/27216585 http://dx.doi.org/10.1038/srep26403 |
_version_ | 1782433415524515840 |
---|---|
author | Briard, Jennie G. Fernandez, Michael De Luna, Phil Woo, Tom. K. Ben, Robert N. |
author_facet | Briard, Jennie G. Fernandez, Michael De Luna, Phil Woo, Tom. K. Ben, Robert N. |
author_sort | Briard, Jennie G. |
collection | PubMed |
description | Ice recrystallization is the main contributor to cell damage and death during the cryopreservation of cells and tissues. Over the past five years, many small carbohydrate-based molecules were identified as ice recrystallization inhibitors and several were shown to reduce cryoinjury during the cryopreservation of red blood cells (RBCs) and hematopoietic stems cells (HSCs). Unfortunately, clear structure-activity relationships have not been identified impeding the rational design of future compounds possessing ice recrystallization inhibition (IRI) activity. A set of 124 previously synthesized compounds with known IRI activities were used to calibrate 3D-QSAR classification models using GRid INdependent Descriptors (GRIND) derived from DFT level quantum mechanical calculations. Partial least squares (PLS) model was calibrated with 70% of the data set which successfully identified 80% of the IRI active compounds with a precision of 0.8. This model exhibited good performance in screening the remaining 30% of the data set with 70% of active additives successfully recovered with a precision of ~0.7 and specificity of 0.8. The model was further applied to screen a new library of aryl-alditol molecules which were then experimentally synthesized and tested with a success rate of 82%. Presented is the first computer-aided high-throughput experimental screening for novel IRI active compounds. |
format | Online Article Text |
id | pubmed-4877635 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-48776352016-06-08 QSAR Accelerated Discovery of Potent Ice Recrystallization Inhibitors Briard, Jennie G. Fernandez, Michael De Luna, Phil Woo, Tom. K. Ben, Robert N. Sci Rep Article Ice recrystallization is the main contributor to cell damage and death during the cryopreservation of cells and tissues. Over the past five years, many small carbohydrate-based molecules were identified as ice recrystallization inhibitors and several were shown to reduce cryoinjury during the cryopreservation of red blood cells (RBCs) and hematopoietic stems cells (HSCs). Unfortunately, clear structure-activity relationships have not been identified impeding the rational design of future compounds possessing ice recrystallization inhibition (IRI) activity. A set of 124 previously synthesized compounds with known IRI activities were used to calibrate 3D-QSAR classification models using GRid INdependent Descriptors (GRIND) derived from DFT level quantum mechanical calculations. Partial least squares (PLS) model was calibrated with 70% of the data set which successfully identified 80% of the IRI active compounds with a precision of 0.8. This model exhibited good performance in screening the remaining 30% of the data set with 70% of active additives successfully recovered with a precision of ~0.7 and specificity of 0.8. The model was further applied to screen a new library of aryl-alditol molecules which were then experimentally synthesized and tested with a success rate of 82%. Presented is the first computer-aided high-throughput experimental screening for novel IRI active compounds. Nature Publishing Group 2016-05-24 /pmc/articles/PMC4877635/ /pubmed/27216585 http://dx.doi.org/10.1038/srep26403 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Briard, Jennie G. Fernandez, Michael De Luna, Phil Woo, Tom. K. Ben, Robert N. QSAR Accelerated Discovery of Potent Ice Recrystallization Inhibitors |
title | QSAR Accelerated Discovery of Potent Ice Recrystallization Inhibitors |
title_full | QSAR Accelerated Discovery of Potent Ice Recrystallization Inhibitors |
title_fullStr | QSAR Accelerated Discovery of Potent Ice Recrystallization Inhibitors |
title_full_unstemmed | QSAR Accelerated Discovery of Potent Ice Recrystallization Inhibitors |
title_short | QSAR Accelerated Discovery of Potent Ice Recrystallization Inhibitors |
title_sort | qsar accelerated discovery of potent ice recrystallization inhibitors |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4877635/ https://www.ncbi.nlm.nih.gov/pubmed/27216585 http://dx.doi.org/10.1038/srep26403 |
work_keys_str_mv | AT briardjennieg qsaraccelerateddiscoveryofpotenticerecrystallizationinhibitors AT fernandezmichael qsaraccelerateddiscoveryofpotenticerecrystallizationinhibitors AT delunaphil qsaraccelerateddiscoveryofpotenticerecrystallizationinhibitors AT wootomk qsaraccelerateddiscoveryofpotenticerecrystallizationinhibitors AT benrobertn qsaraccelerateddiscoveryofpotenticerecrystallizationinhibitors |