Grant: Project Grant
McGill University
$1,124,550.00
Impact of CKAP2 on mitotic spindle architecture
EF 2022-23
Résumé
When cells divide, the DNA in form of chromosomes is pulled into the two new daughter cells. The machinery, that exerts the force necessary for separating the chromosomes is made from tiny flexible tubes that we call microtubules.
Microtubules have to form and grow very quickly and precisely during cell division. They must be very stable and very dynamic at the same time and constantly be replenished.
To make these microtubules, help them grow, stabilize them and ultimately break them apart again, cells use an army of proteins, called MAPs (microtubule-associated proteins).
While we know some MAPs, many of these proteins are still not well characterized or completely unknown. We are investigating a MAP that makes new microtubules and helps them grow extremely fast. The same MAP is involved in causing several types of cancer as well as making these cancers more aggressive.
We will attempt to solve how this protein makes microtubules grow, how it is involved in building the machinery that divides chromosomes, why cell division is not working well when the protein is misregulated and how that can cause cancer. In addition, we will solve the structure of that protein bound to microtubules, which might help develop new anti-cancer drugs.
Programme
Project Grant
Bénéficiaire
Emplacement
Quebec, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
CIHR Funding Decisions Database
Tel que publié
Id
479329
Name
Bechstedt Susanne
Region
Québec
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Cancer Research
Theme2
Biomedical
Prcname2
Cell Biology - Molecular/Fundamental
Projecttitle
Impact of CKAP2 on mitotic spindle architecture
Programtype2
Operating Grants
Orgnameinp2
McGill University
Cihramount2
$1,124,550
Cihrequipment2
$0
Programname2
Project Grant
Keyworddelim
Microtubule-Associated Proteins; Microtubules; Mitotic Spindles
Abstract
When cells divide, the DNA in form of chromosomes is pulled into the two new daughter cells. The machinery, that exerts the force necessary for separating the chromosomes is made from tiny flexible tubes that we call microtubules.
Microtubules have to form and grow very quickly and precisely during cell division. They must be very stable and very dynamic at the same time and constantly be replenished.
To make these microtubules, help them grow, stabilize them and ultimately break them apart again, cells use an army of proteins, called MAPs (microtubule-associated proteins).
While we know some MAPs, many of these proteins are still not well characterized or completely unknown. We are investigating a MAP that makes new microtubules and helps them grow extremely fast. The same MAP is involved in causing several types of cancer as well as making these cancers more aggressive.
We will attempt to solve how this protein makes microtubules grow, how it is involved in building the machinery that divides chromosomes, why cell division is not working well when the protein is misregulated and how that can cause cancer. In addition, we will solve the structure of that protein bound to microtubules, which might help develop new anti-cancer drugs.
Competitiondate
202303
Approvedterm2
5 yrs 0 mth
Pinamesdelim
Bechstedt, Susanne
Approvedterm
5 ans 0 mois
Cihrcontribution2
~ $1,124,550~ $0~