Mitochondrial Biochemistry: From Mechanisms to Disease

NIH RePORTER · NIH · R35 · $381,252 · view on reporter.nih.gov ↗

Abstract

Project Summary/Abstract Mitochondria are the major source of cellular energy and are also one of the major sites of defects leading to age-related disorders. In spite of the obvious importance, roughly 1/3 of the proteins found there have no know function. One major goal of the Rutter laboratory is to define the functions of a subset of these proteins, particularly those that are highly evolutionarily conserved across eukaryotic species. We have begun this process and have defined the molecular functions of ten mitochondrial protein families. These have included important factors for OXPHOS complex assembly, mitochondrial quality control, metabolic regulation and others. These discoveries have enabled our laboratory and many others to develop new understanding of normal human physiology and disease pathophysiology, including the discovery of two new human disease genes. The proposed future activities are a combination of continuing our efforts to define the functions of previously unstudied mitochondrial proteins and leveraging our previous discoveries toward a better understanding of mitochondrial biology and its physiological manifestations.

Key facts

NIH application ID
9893007
Project number
5R35GM131854-02
Recipient
UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH
Principal Investigator
Jared P Rutter
Activity code
R35
Funding institute
NIH
Fiscal year
2020
Award amount
$381,252
Award type
5
Project period
2019-04-01 → 2024-03-31