Structure- based inhibitor design for key enzymes of <em>Tryposoma brucei</em>

<p>Human African trypanosomiasis (HAT) also known as sleeping sickness is caused by a subspecies of <em>Trypanosoma brucei</em>. These parasites are transmitted by tsetse flies and endanger over 60 million people in Sub-Saharan Africa. Untreated, sleeping sickness is fatal, causing at least 48.000 deaths per year. Its treatment remains complicated since the currently available drugs show high toxicity and are too expensive to be ubiquitously distributed in the affected third world economies. Additionally, emerging drug resistance towards the most clinically relevant anti HAT drugs, drastically limits treatment options and makes it imperative to conduct research to find safer and more efficient drugs to treat this terrible disease.<br/> This thesis describes the hit identification and hit validation for two validated<br/> targets for HAT: <em>Tb</em>6PGDH and <em>Tb</em>UGP. For hit identification different techniques like in silico virtual screening, NMR lead-like fragment screening and HTS were used. For <em>Tb</em>UGP a very first drug-like, competitive inhibitor with a pIC50 of 3.53±0.04 and a Hill slope of 1.1±0.1 was discovered. Additionally this thesis describes the determination and validation of the in silico proposed binding mode using mutation studies and crystallisation techniques.</p>

Name dc:type.qualificationname

Doctor of Philosophy

Level dc:type.qualificationlevel

Doctoral Thesis

Grantor dc:publisher.institution

University of Dundee

Year dc:date.issued

2014

Author dc:creator

• Striker, Waldemar

Language dc:language

eng

Identifier

oai:discovery.dundee.ac.uk:studenttheses/8a379fb4-7e59-4005-8e2c-1a2b8a6116b8

OAI identifier oai:identifier

oai:discovery.dundee.ac.uk:studenttheses/8a379fb4-7e59-4005-8e2c-1a2b8a6116b8