Screening of the whole human cytochrome P450 complement (CYPome) with enzyme bag cocktails
We have previously introduced the use of permeabilized fission yeast cells (enzyme bags) that recombinantly express full-length CYPs for drug metabolism studies. Such enzyme bags are cells with pores that function as enzymes in situ. They can easily be prepared without a need for ultracentrifugation...
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doaj-1e8d79112a1c40fda86d3b8571b693ba2021-04-02T16:47:57ZengElsevierJournal of Pharmaceutical Analysis2095-17792020-06-01103271276Screening of the whole human cytochrome P450 complement (CYPome) with enzyme bag cocktailsSangeeta Shrestha Sharma0Shishir Sharma1Matthias Bureik2School of Pharmaceutical Science and Technology, Health Sciences Platform, Tianjin University, Tianjin, 300072, ChinaSchool of Pharmaceutical Science and Technology, Health Sciences Platform, Tianjin University, Tianjin, 300072, ChinaCorresponding author.; School of Pharmaceutical Science and Technology, Health Sciences Platform, Tianjin University, Tianjin, 300072, ChinaWe have previously introduced the use of permeabilized fission yeast cells (enzyme bags) that recombinantly express full-length CYPs for drug metabolism studies. Such enzyme bags are cells with pores that function as enzymes in situ. They can easily be prepared without a need for ultracentrifugation and may be used in similar protocols as microsomes. In this study we report the preparation of enzyme bag cocktails that permit the testing of multiple CYPs in a single enzyme bag reaction. Moreover, we established a convenient testing scheme that permits a rapid screen of all human CYPs for activity towards any given candidate substrate. An important aspect of this approach is the reduction of individual CYP test assays. If a cocktail containing many CYPs tests negative, it follows that all CYPs included in that cocktail need not be tested individually, thus saving time and resources. The new protocol was validated using two probe substrates.http://www.sciencedirect.com/science/article/pii/S2095177920301696Cytochrome P450Drug metabolismFission yeastLuminescenceProluciferin |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Sangeeta Shrestha Sharma Shishir Sharma Matthias Bureik |
spellingShingle |
Sangeeta Shrestha Sharma Shishir Sharma Matthias Bureik Screening of the whole human cytochrome P450 complement (CYPome) with enzyme bag cocktails Journal of Pharmaceutical Analysis Cytochrome P450 Drug metabolism Fission yeast Luminescence Proluciferin |
author_facet |
Sangeeta Shrestha Sharma Shishir Sharma Matthias Bureik |
author_sort |
Sangeeta Shrestha Sharma |
title |
Screening of the whole human cytochrome P450 complement (CYPome) with enzyme bag cocktails |
title_short |
Screening of the whole human cytochrome P450 complement (CYPome) with enzyme bag cocktails |
title_full |
Screening of the whole human cytochrome P450 complement (CYPome) with enzyme bag cocktails |
title_fullStr |
Screening of the whole human cytochrome P450 complement (CYPome) with enzyme bag cocktails |
title_full_unstemmed |
Screening of the whole human cytochrome P450 complement (CYPome) with enzyme bag cocktails |
title_sort |
screening of the whole human cytochrome p450 complement (cypome) with enzyme bag cocktails |
publisher |
Elsevier |
series |
Journal of Pharmaceutical Analysis |
issn |
2095-1779 |
publishDate |
2020-06-01 |
description |
We have previously introduced the use of permeabilized fission yeast cells (enzyme bags) that recombinantly express full-length CYPs for drug metabolism studies. Such enzyme bags are cells with pores that function as enzymes in situ. They can easily be prepared without a need for ultracentrifugation and may be used in similar protocols as microsomes. In this study we report the preparation of enzyme bag cocktails that permit the testing of multiple CYPs in a single enzyme bag reaction. Moreover, we established a convenient testing scheme that permits a rapid screen of all human CYPs for activity towards any given candidate substrate. An important aspect of this approach is the reduction of individual CYP test assays. If a cocktail containing many CYPs tests negative, it follows that all CYPs included in that cocktail need not be tested individually, thus saving time and resources. The new protocol was validated using two probe substrates. |
topic |
Cytochrome P450 Drug metabolism Fission yeast Luminescence Proluciferin |
url |
http://www.sciencedirect.com/science/article/pii/S2095177920301696 |
work_keys_str_mv |
AT sangeetashresthasharma screeningofthewholehumancytochromep450complementcypomewithenzymebagcocktails AT shishirsharma screeningofthewholehumancytochromep450complementcypomewithenzymebagcocktails AT matthiasbureik screeningofthewholehumancytochromep450complementcypomewithenzymebagcocktails |
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