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Binding and inhibition of spermidine synthase from Plasmodium falciparum and implications for in vitro inhibitor testing

Sprenger, Janina LU ; Carey, Jannette ; Svensson, Bo ; Wengel, Verena and Persson, Lo LU (2016) In PLoS ONE 11(9).
Abstract

The aminopropyltransferase spermidine synthase (SpdS) is a promising drug target in cancer and in protozoan diseases including malaria. Plasmodium falciparum SpdS (PfSpdS) transfers the aminopropyl group of decarboxylated S-adenosylmethionine (dcAdoMet) to putrescine or to spermidine to form spermidine or spermine, respectively. In an effort to understand why efficient inhibitors of PfSpdS have been elusive, the present study uses enzyme activity assays and isothermal titration calorimetry with verified or predicted inhibitors of PfSpdS to analyze the relationship between binding affinity as assessed by KD and inhibitory activity as assessed by IC50. The results show that some predicted inhibitors bind to the enzyme with high... (More)

The aminopropyltransferase spermidine synthase (SpdS) is a promising drug target in cancer and in protozoan diseases including malaria. Plasmodium falciparum SpdS (PfSpdS) transfers the aminopropyl group of decarboxylated S-adenosylmethionine (dcAdoMet) to putrescine or to spermidine to form spermidine or spermine, respectively. In an effort to understand why efficient inhibitors of PfSpdS have been elusive, the present study uses enzyme activity assays and isothermal titration calorimetry with verified or predicted inhibitors of PfSpdS to analyze the relationship between binding affinity as assessed by KD and inhibitory activity as assessed by IC50. The results show that some predicted inhibitors bind to the enzyme with high affinity but are poor inhibitors. Binding studies with PfSpdS substrates and products strongly support an ordered sequential mechanism in which the aminopropyl donor (dcAdoMet) site must be occupied before the aminopropyl acceptor (putrescine) site can be occupied. Analysis of the results also shows that the ordered sequential mechanism adequately accounts for the complex relationship between IC50 and KD and may explain the limited success of previous efforts at structure-based inhibitor design for PfSpdS. Based on PfSpdS active-site occupancy, we suggest a classification of ligands that can help to predict the KD-IC50 relations in future design of new inhibitors. The present findings may be relevant for other drug targets that follow an ordered sequential mechanism.

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organization
publishing date
type
Contribution to journal
publication status
published
subject
in
PLoS ONE
volume
11
issue
9
article number
e0163442
publisher
Public Library of Science (PLoS)
external identifiers
  • scopus:84992111613
  • pmid:27661085
  • wos:000383893500034
ISSN
1932-6203
DOI
10.1371/journal.pone.0163442
language
English
LU publication?
yes
id
4ec4530b-7158-482b-a766-86ca371532a1
date added to LUP
2016-11-04 09:22:28
date last changed
2024-11-16 09:59:24
@article{4ec4530b-7158-482b-a766-86ca371532a1,
  abstract     = {{<p>The aminopropyltransferase spermidine synthase (SpdS) is a promising drug target in cancer and in protozoan diseases including malaria. Plasmodium falciparum SpdS (PfSpdS) transfers the aminopropyl group of decarboxylated S-adenosylmethionine (dcAdoMet) to putrescine or to spermidine to form spermidine or spermine, respectively. In an effort to understand why efficient inhibitors of PfSpdS have been elusive, the present study uses enzyme activity assays and isothermal titration calorimetry with verified or predicted inhibitors of PfSpdS to analyze the relationship between binding affinity as assessed by KD and inhibitory activity as assessed by IC<sub>50</sub>. The results show that some predicted inhibitors bind to the enzyme with high affinity but are poor inhibitors. Binding studies with PfSpdS substrates and products strongly support an ordered sequential mechanism in which the aminopropyl donor (dcAdoMet) site must be occupied before the aminopropyl acceptor (putrescine) site can be occupied. Analysis of the results also shows that the ordered sequential mechanism adequately accounts for the complex relationship between IC50 and KD and may explain the limited success of previous efforts at structure-based inhibitor design for PfSpdS. Based on PfSpdS active-site occupancy, we suggest a classification of ligands that can help to predict the K<sub>D</sub>-IC<sub>50</sub> relations in future design of new inhibitors. The present findings may be relevant for other drug targets that follow an ordered sequential mechanism.</p>}},
  author       = {{Sprenger, Janina and Carey, Jannette and Svensson, Bo and Wengel, Verena and Persson, Lo}},
  issn         = {{1932-6203}},
  language     = {{eng}},
  month        = {{09}},
  number       = {{9}},
  publisher    = {{Public Library of Science (PLoS)}},
  series       = {{PLoS ONE}},
  title        = {{Binding and inhibition of spermidine synthase from Plasmodium falciparum and implications for in vitro inhibitor testing}},
  url          = {{http://dx.doi.org/10.1371/journal.pone.0163442}},
  doi          = {{10.1371/journal.pone.0163442}},
  volume       = {{11}},
  year         = {{2016}},
}