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Grant: Travel Awards - Institute Community Support

University of Saskatchewan

$3,000.00

APOBEC3 Dynamics: APOBEC3 Interactions and HIV Vif Antagonism

FY 2024-25

Summary
HIV, the virus that causes AIDS, remains a major global health issue because it can escape the body's natural defense system. One way HIV does this is through a protein called Viral Infectivity Factor (Vif), which targets and neutralizes certain enzymes in the human body, known as APOBEC3 enzymes. These A3 enzymes help stop HIV from replicating by modifying and mutating the virus's genetic material during infection. Vif prevents APOBEC3 restriction activity by marking them for destruction and degradation. Some of these APOBEC3 enzymes, like APOBEC3F and APOBEC3G, can work together in pairs, which makes them more effective at fighting HIV and helps A3F resist being destroyed by Vif. This study looks at how APOBEC3F and APOBEC3G interact and how this protects APOBEC3F from Vif. We found that, contrary to what was previously thought, a part of APOBEC3F known as the N-terminal domain plays a key role in both pairing with APOBEC3G and interacting with Vif. These findings offer new insights into how the body's defense systems work together to suppress HIV, and they could help guide the development of new treatments that block the ability of HIV to evade the immune system.
Program
Travel Awards - Institute Community Support
Location
Saskatchewan, Canada
Recipient Type
Academia
Type
Grant
Source
CIHR Funding Decisions Database

As published

Id
521480
Name
Yousefi Maryam
Region
Saskatchewan
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Infection and Immunity
Theme2
Biomedical
Prcname2
Travel Awards - Institute Community Support
Projecttitle
APOBEC3 Dynamics: APOBEC3 Interactions and HIV Vif Antagonism
Programtype2
Undefined
Orgnameinp2
University of Saskatchewan
Cihramount2
$3,000
Cihrequipment2
$0
Programname2
Travel Awards - Institute Community Support
Keyworddelim
Ics Travel Awards
Abstract
HIV, the virus that causes AIDS, remains a major global health issue because it can escape the body's natural defense system. One way HIV does this is through a protein called Viral Infectivity Factor (Vif), which targets and neutralizes certain enzymes in the human body, known as APOBEC3 enzymes. These A3 enzymes help stop HIV from replicating by modifying and mutating the virus's genetic material during infection. Vif prevents APOBEC3 restriction activity by marking them for destruction and degradation. Some of these APOBEC3 enzymes, like APOBEC3F and APOBEC3G, can work together in pairs, which makes them more effective at fighting HIV and helps A3F resist being destroyed by Vif. This study looks at how APOBEC3F and APOBEC3G interact and how this protects APOBEC3F from Vif. We found that, contrary to what was previously thought, a part of APOBEC3F known as the N-terminal domain plays a key role in both pairing with APOBEC3G and interacting with Vif. These findings offer new insights into how the body's defense systems work together to suppress HIV, and they could help guide the development of new treatments that block the ability of HIV to evade the immune system.
Competitiondate
202501
Approvedterm2
1 yr 0 mth
Pinamesdelim
Yousefi, Maryam
Approvedterm
1 an 0 mois
Cihrcontribution2
MI #3~ $3,000~ $0~
University of Saskatchewan - $3,000 Grant (2024-25) | Canada Spends