NADH dehydrogenase as a molecular target for artemisinin related antimalaria drug screening in a yeast model / Ummul Hanan Mohamad

Artemisinin is currently the only effective drug against malaria. However, artemisininresistant Plasmodium had begun to emerge in many malaria endemic areas. Discovery of new anti-malarial with artemisinin-like activity had been slow as the molecular target of artemisinin was yet to be established....

Full description

Saved in:
Bibliographic Details
Main Author: Mohamad, Ummul Hanan
Format: Thesis
Language:English
Published: 2015
Subjects:
Online Access:https://ir.uitm.edu.my/id/eprint/15930/1/TP_UMMUL%20HANAN%20MOHAMAD%20AS%2015_5.PDF
https://ir.uitm.edu.my/id/eprint/15930/
Tags: Add Tag
No Tags, Be the first to tag this record!
Institution: Universiti Teknologi Mara
Language: English
id my.uitm.ir.15930
record_format eprints
spelling my.uitm.ir.159302022-03-10T02:13:18Z https://ir.uitm.edu.my/id/eprint/15930/ NADH dehydrogenase as a molecular target for artemisinin related antimalaria drug screening in a yeast model / Ummul Hanan Mohamad Mohamad, Ummul Hanan Bacteria Artemisinin is currently the only effective drug against malaria. However, artemisininresistant Plasmodium had begun to emerge in many malaria endemic areas. Discovery of new anti-malarial with artemisinin-like activity had been slow as the molecular target of artemisinin was yet to be established. In addition, studies on the malaria causative agent were also hampered because Plasmodium was difficult to culture invitro. Therefore, this research aims to develop a reliable yeast screening system to help clarify artemisinin mode of action as well as accelerate the discovery of potential anti-malaria with artemisinin-like properties. The NADH dehydrogenase enzyme, which was coded by NDE1 and NDI1, in Saccharomyces cerevisiae as thought to be a major molecular target for artemisinin A yeast system was constructed in which the efflux pump regulator genes, PDR1 and PDR3, and either NDE1 or NDI1 were deleted. Absence of the PDR1 and PDR3 genes minimized the ability of yeast to remove the test drugs into the extracellular environment, thus the drug effect could be clearly observed. From the study, ApdrlApdr3Andel or ApdrlApdr3Andil knock-out tolerated 12 artemisinin and 4 |xM dihydroartemisinin in contrast to ApdrlApdr3. Hence, ts.pdrlts.pdr3 and ApdrlA.pdr3Andel were chosen to serve as the screening panels. Several compounds were found to possess artemisinin-like activities. These included black seed oil, black pepper and mangosteen. Since NADH dehydrogenase genes in yeast were homologous to Plasmodium NDH2 gene, it was assumed that any effect towards the yeast proteins may be reflective of a similar effect towards Plasmodium protein Further validation demonstrated that the cloned NDE1 gene partially restored the yeast susceptibility to artemisinin derivative, dihydroartemisinin. Real-time PCR revealed that the yeast with cloned NDE1 expressed NADH dehydrogenase albeit at 32-fold lower than the wild-type. Following that, random mutation to NDE1 gene showed that most mutation was single nucleotide deletion that altered the protein sequence to produce non-functional (due to stop codons) or missense (due to different amino acid sequence) protein to resist artemisinin derivative. 2015 Thesis NonPeerReviewed text en https://ir.uitm.edu.my/id/eprint/15930/1/TP_UMMUL%20HANAN%20MOHAMAD%20AS%2015_5.PDF ID15930 Mohamad, Ummul Hanan (2015) NADH dehydrogenase as a molecular target for artemisinin related antimalaria drug screening in a yeast model / Ummul Hanan Mohamad. PhD thesis, thesis, Universiti Teknologi MARA.
institution Universiti Teknologi Mara
building Tun Abdul Razak Library
collection Institutional Repository
continent Asia
country Malaysia
content_provider Universiti Teknologi Mara
content_source UiTM Institutional Repository
url_provider http://ir.uitm.edu.my/
language English
topic Bacteria
spellingShingle Bacteria
Mohamad, Ummul Hanan
NADH dehydrogenase as a molecular target for artemisinin related antimalaria drug screening in a yeast model / Ummul Hanan Mohamad
description Artemisinin is currently the only effective drug against malaria. However, artemisininresistant Plasmodium had begun to emerge in many malaria endemic areas. Discovery of new anti-malarial with artemisinin-like activity had been slow as the molecular target of artemisinin was yet to be established. In addition, studies on the malaria causative agent were also hampered because Plasmodium was difficult to culture invitro. Therefore, this research aims to develop a reliable yeast screening system to help clarify artemisinin mode of action as well as accelerate the discovery of potential anti-malaria with artemisinin-like properties. The NADH dehydrogenase enzyme, which was coded by NDE1 and NDI1, in Saccharomyces cerevisiae as thought to be a major molecular target for artemisinin A yeast system was constructed in which the efflux pump regulator genes, PDR1 and PDR3, and either NDE1 or NDI1 were deleted. Absence of the PDR1 and PDR3 genes minimized the ability of yeast to remove the test drugs into the extracellular environment, thus the drug effect could be clearly observed. From the study, ApdrlApdr3Andel or ApdrlApdr3Andil knock-out tolerated 12 artemisinin and 4 |xM dihydroartemisinin in contrast to ApdrlApdr3. Hence, ts.pdrlts.pdr3 and ApdrlA.pdr3Andel were chosen to serve as the screening panels. Several compounds were found to possess artemisinin-like activities. These included black seed oil, black pepper and mangosteen. Since NADH dehydrogenase genes in yeast were homologous to Plasmodium NDH2 gene, it was assumed that any effect towards the yeast proteins may be reflective of a similar effect towards Plasmodium protein Further validation demonstrated that the cloned NDE1 gene partially restored the yeast susceptibility to artemisinin derivative, dihydroartemisinin. Real-time PCR revealed that the yeast with cloned NDE1 expressed NADH dehydrogenase albeit at 32-fold lower than the wild-type. Following that, random mutation to NDE1 gene showed that most mutation was single nucleotide deletion that altered the protein sequence to produce non-functional (due to stop codons) or missense (due to different amino acid sequence) protein to resist artemisinin derivative.
format Thesis
author Mohamad, Ummul Hanan
author_facet Mohamad, Ummul Hanan
author_sort Mohamad, Ummul Hanan
title NADH dehydrogenase as a molecular target for artemisinin related antimalaria drug screening in a yeast model / Ummul Hanan Mohamad
title_short NADH dehydrogenase as a molecular target for artemisinin related antimalaria drug screening in a yeast model / Ummul Hanan Mohamad
title_full NADH dehydrogenase as a molecular target for artemisinin related antimalaria drug screening in a yeast model / Ummul Hanan Mohamad
title_fullStr NADH dehydrogenase as a molecular target for artemisinin related antimalaria drug screening in a yeast model / Ummul Hanan Mohamad
title_full_unstemmed NADH dehydrogenase as a molecular target for artemisinin related antimalaria drug screening in a yeast model / Ummul Hanan Mohamad
title_sort nadh dehydrogenase as a molecular target for artemisinin related antimalaria drug screening in a yeast model / ummul hanan mohamad
publishDate 2015
url https://ir.uitm.edu.my/id/eprint/15930/1/TP_UMMUL%20HANAN%20MOHAMAD%20AS%2015_5.PDF
https://ir.uitm.edu.my/id/eprint/15930/
_version_ 1728054726364233728