Grant: Discovery Grants Program - Individual
University of British Columbia
$84,000.00
Studies on Enzyme Mechanism and Inhibitor Design
FY 2016-17
Summary
This proposal is divided into three sections. The first section describes our studies on enzymes that produce alkaloids. Alkaloids are nitrogen-containing natural products primarily produced by plants and fungi. They often possess potent biological activities and many have been used as valuable pharmaceuticals (morphine/pain, vinblastine/cancer, ergotamine/migraines). We are studying the enzymes involved in the biosynthesis of the indole alkaloids such as ergotamine. We have discovered that these enzymes can produce novel alkaloids that may have unique biological properties. By understanding the details of how these enzymes function, we may be able to utilize them in the production of new bioactive compounds. The second section involves studies on the biosynthesis of menaquinone (vitamin K2) in the pathogenic bacteria that are responsible for ulcers and food poisoning. These bacteria require menaquinone for respiration and without it they cannot survive. We are investigating the enzymes involved in menaquinone biosynthesis in these organisms since these are attractive targets for inhibitor design. Such inhibitors would prevent the enzymes from operating and would therefore serve as antibiotics against these organisms. In our initial studies we outlined the correct biosynthetic pathway for the formation of this vitamin, and in ongoing work we are studying individual enzymes in the pathway so that inhibitors can be designed. The third section involves studies on tubulin-modifying enzymes. Microtubules form the cytoskeleton of human cells and are absolutely required for proper cell division. For this reason, compounds that interfere with proper microtubule formation act as potent anticancer agents (vinblastine, taxol). Microtubules are generated by the spontaneous self-assembly of tubulin. We are studying a group of enzymes that chemically modify tubulin and therefore control its physical properties. We are preparing inhibitor molecules that will interfere with the action of these enzymes and we anticipate that such compounds will be cytotoxic. This could potentially serve as a new approach towards treating cancer.
Program
Discovery Grants Program - Individual
Recipient
Location
British Columbia, Canada
Recipient Type
Academia
Type
Grant
Source
NSERC's Awards Data
As published
Application id
138133-2013
Name nom
Tanner, Martin
Department département
Chemistry
Organization id
2
Institution établissement
University of British Columbia
Province en
British Columbia
Province fr
Colombie-Britannique
Country en
CANADA
Country fr
CANADA
Fiscal year exercice financier
2016
Competition year année de concours
2013
Award amount
84000
Program id
RGPIN
Program name en
Discovery Grants Program - Individual
Program name fr
Programme de subventions à la découverte - individuelles
Group en
Discovery grants programs
Group fr
Programmes de subventions à la découverte
Committee code
1504
Committee name en
Chemistry
Committee name fr
Chimie
Area of application code
1200
Area of application group en
Advancement of knowledge
Area of application group fr
Avancement des connaissances
Area of application en
Advancement of knowledge
Area of application fr
Avancement des connaissances
Research subject code
3705
Research subject group en
Organic chemistry
Research subject group fr
Chimie organique
Research subject en
Bio-organic chemistry
Research subject fr
Chimie bio-organique
Partie
4
Nb partie
6
Application title
Studies on Enzyme Mechanism and Inhibitor Design
Keyword
NSERC
Application summary
This proposal is divided into three sections. The first section describes our studies on enzymes that produce alkaloids. Alkaloids are nitrogen-containing natural products primarily produced by plants and fungi. They often possess potent biological activities and many have been used as valuable pharmaceuticals (morphine/pain, vinblastine/cancer, ergotamine/migraines). We are studying the enzymes involved in the biosynthesis of the indole alkaloids such as ergotamine. We have discovered that these enzymes can produce novel alkaloids that may have unique biological properties. By understanding the details of how these enzymes function, we may be able to utilize them in the production of new bioactive compounds. The second section involves studies on the biosynthesis of menaquinone (vitamin K2) in the pathogenic bacteria that are responsible for ulcers and food poisoning. These bacteria require menaquinone for respiration and without it they cannot survive. We are investigating the enzymes involved in menaquinone biosynthesis in these organisms since these are attractive targets for inhibitor design. Such inhibitors would prevent the enzymes from operating and would therefore serve as antibiotics against these organisms. In our initial studies we outlined the correct biosynthetic pathway for the formation of this vitamin, and in ongoing work we are studying individual enzymes in the pathway so that inhibitors can be designed. The third section involves studies on tubulin-modifying enzymes. Microtubules form the cytoskeleton of human cells and are absolutely required for proper cell division. For this reason, compounds that interfere with proper microtubule formation act as potent anticancer agents (vinblastine, taxol). Microtubules are generated by the spontaneous self-assembly of tubulin. We are studying a group of enzymes that chemically modify tubulin and therefore control its physical properties. We are preparing inhibitor molecules that will interfere with the action of these enzymes and we anticipate that such compounds will be cytotoxic. This could potentially serve as a new approach towards treating cancer.