Optimisation of purification of plasmodium falciparum Kelch13 protein for structural analysis
The protozoan Plasmodium falciparum has the potential to cause severe malaria disease which is fatal when untreated. Artemisinin derived from Artemisia annua L. has conventionally been used to combat the disease. However, resistance to Artemisinins originating from Southeast Asia has been devel...
Saved in:
Main Author: | |
---|---|
Other Authors: | |
Format: | Final Year Project |
Language: | English |
Published: |
Nanyang Technological University
2023
|
Subjects: | |
Online Access: | https://hdl.handle.net/10356/166438 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Institution: | Nanyang Technological University |
Language: | English |
id |
sg-ntu-dr.10356-166438 |
---|---|
record_format |
dspace |
spelling |
sg-ntu-dr.10356-1664382023-05-01T15:32:58Z Optimisation of purification of plasmodium falciparum Kelch13 protein for structural analysis Seo, Gilia Min Li Shashi Bhushan School of Biological Sciences SBhushan@ntu.edu.sg Science::Biological sciences The protozoan Plasmodium falciparum has the potential to cause severe malaria disease which is fatal when untreated. Artemisinin derived from Artemisia annua L. has conventionally been used to combat the disease. However, resistance to Artemisinins originating from Southeast Asia has been developing, compromising the fight against malaria. Though Artemisinins is believed to target widespread cellular targets, resistance phenotype has been traced to mutations in the Plasmodium falciparum Kelch13 protein, which is essential for intraerythrocytic growth of the parasite. Unfortunately, the development of new drugs has been impeded by the challenge to express and purify the Kelch13 protein. In this study, strategies to optimise the expression and purification of the Kelch13 protein by modulating cell growth and extraction conditions were proposed. Techniques such as SDS-PAGE, size exclusion chromatography, and negative-stain transmission electron microscopy verified the presence of soluble proteins when low temperature, high nutrient conditions were used in combination with a detergent, reducing agent and high salt buffers. Negative-stain transmission electron microscopy images displayed a largely monomeric structure of the Kelch13 protein in solution. The results obtained in this study proves the ability of the Kelch13 to be expressed in solution as a monomer, empowering future studies in antimalarial drug development. Bachelor of Science in Biological Sciences 2023-04-28T07:24:51Z 2023-04-28T07:24:51Z 2023 Final Year Project (FYP) Seo, G. M. L. (2023). Optimisation of purification of plasmodium falciparum Kelch13 protein for structural analysis. Final Year Project (FYP), Nanyang Technological University, Singapore. https://hdl.handle.net/10356/166438 https://hdl.handle.net/10356/166438 en application/pdf Nanyang Technological University |
institution |
Nanyang Technological University |
building |
NTU Library |
continent |
Asia |
country |
Singapore Singapore |
content_provider |
NTU Library |
collection |
DR-NTU |
language |
English |
topic |
Science::Biological sciences |
spellingShingle |
Science::Biological sciences Seo, Gilia Min Li Optimisation of purification of plasmodium falciparum Kelch13 protein for structural analysis |
description |
The protozoan Plasmodium falciparum has the potential to cause severe malaria
disease which is fatal when untreated. Artemisinin derived from Artemisia annua L.
has conventionally been used to combat the disease. However, resistance to
Artemisinins originating from Southeast Asia has been developing, compromising the
fight against malaria. Though Artemisinins is believed to target widespread cellular
targets, resistance phenotype has been traced to mutations in the Plasmodium
falciparum Kelch13 protein, which is essential for intraerythrocytic growth of the
parasite. Unfortunately, the development of new drugs has been impeded by the
challenge to express and purify the Kelch13 protein. In this study, strategies to
optimise the expression and purification of the Kelch13 protein by modulating cell
growth and extraction conditions were proposed. Techniques such as SDS-PAGE,
size exclusion chromatography, and negative-stain transmission electron microscopy
verified the presence of soluble proteins when low temperature, high nutrient
conditions were used in combination with a detergent, reducing agent and high salt
buffers. Negative-stain transmission electron microscopy images displayed a largely
monomeric structure of the Kelch13 protein in solution. The results obtained in this
study proves the ability of the Kelch13 to be expressed in solution as a monomer,
empowering future studies in antimalarial drug development. |
author2 |
Shashi Bhushan |
author_facet |
Shashi Bhushan Seo, Gilia Min Li |
format |
Final Year Project |
author |
Seo, Gilia Min Li |
author_sort |
Seo, Gilia Min Li |
title |
Optimisation of purification of plasmodium falciparum Kelch13 protein for structural analysis |
title_short |
Optimisation of purification of plasmodium falciparum Kelch13 protein for structural analysis |
title_full |
Optimisation of purification of plasmodium falciparum Kelch13 protein for structural analysis |
title_fullStr |
Optimisation of purification of plasmodium falciparum Kelch13 protein for structural analysis |
title_full_unstemmed |
Optimisation of purification of plasmodium falciparum Kelch13 protein for structural analysis |
title_sort |
optimisation of purification of plasmodium falciparum kelch13 protein for structural analysis |
publisher |
Nanyang Technological University |
publishDate |
2023 |
url |
https://hdl.handle.net/10356/166438 |
_version_ |
1765213864728723456 |