Grant: Project Grant
University of Toronto
$1,139,850.00
Structure and guided engineering of oncostatin M in inflammatory disease
FY 2025-26
Summary
Inflammation and fibrosis, which involve tissue damage and scarring, are regulated by a protein called Oncostatin M (OSM). OSM, part of a larger family of proteins called cytokines, sends signals through two different receptor groups: one that reduces inflammation and another that can cause harmful inflammation. Because OSM can send such different signals, it has been challenging to use it directly as a treatment.
Our research aims to understand how OSM works at a molecular level to create new therapies for inflammatory diseases and fibrosis. We will use a technique called cryo-electron microscopy (cryoEM) to observe the detailed structures of OSM and how it interacts with its receptors. This will help us understand how OSM signals in both beneficial and harmful ways.
We will study the structures of OSM with its receptors to understand how it can cause different effects in the body. Additionally, we will explore how certain drugs and antibodies that block OSM work, which can guide the development of new treatments. Finally, we will design new versions of OSM that only send beneficial signals, avoiding the harmful ones.
This research will provide crucial insights into how OSM works and lead to innovative treatments for inflammation and fibrosis, potentially transforming care for patients with these conditions.
Department
Program
Project Grant
Recipient
Location
Ontario, Canada
Recipient Type
Academia
Type
Grant
Source
CIHR Funding Decisions Database
As published
Id
532107
Name
Caveney Nathanael
Region
Ontario
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Infection and Immunity
Theme2
Biomedical
Prcname2
Biochemistry & Molecular Biology - A
Projecttitle
Structure and guided engineering of oncostatin M in inflammatory disease
Programtype2
Operating Grants
Orgnameinp2
University of Toronto
Cihramount2
$1,139,850
Cihrequipment2
$0
Programname2
Project Grant
Keyworddelim
Cell Signalling; Cryoem; Oncostatin M; Protein Engineering; Structural Biology
Abstract
Inflammation and fibrosis, which involve tissue damage and scarring, are regulated by a protein called Oncostatin M (OSM). OSM, part of a larger family of proteins called cytokines, sends signals through two different receptor groups: one that reduces inflammation and another that can cause harmful inflammation. Because OSM can send such different signals, it has been challenging to use it directly as a treatment.
Our research aims to understand how OSM works at a molecular level to create new therapies for inflammatory diseases and fibrosis. We will use a technique called cryo-electron microscopy (cryoEM) to observe the detailed structures of OSM and how it interacts with its receptors. This will help us understand how OSM signals in both beneficial and harmful ways.
We will study the structures of OSM with its receptors to understand how it can cause different effects in the body. Additionally, we will explore how certain drugs and antibodies that block OSM work, which can guide the development of new treatments. Finally, we will design new versions of OSM that only send beneficial signals, avoiding the harmful ones.
This research will provide crucial insights into how OSM works and lead to innovative treatments for inflammation and fibrosis, potentially transforming care for patients with these conditions.
Competitiondate
202509
Approvedterm2
5 yrs 0 mth
Pinamesdelim
Caveney, Nathanael
Approvedterm
5 ans 0 mois
Cihrcontribution2
~ $1,139,850~ $0~