Phase behavior of proteins in crowded environments

Active Project Grant Awarded Last action

Award ID
R15GM154243
Recipient
Awarding agency
Obligated
$441,108

Award facts

Assistance listing
93.859 Biomedical Research and Research Training
Completion date 71% complete
Place of performance
Baton Rouge, LA 70803, USA

Award details come from USAspending.gov.

About this award

This federal Project Grant award, provided by the National Institute of General Medical Sciences (NIGMS) under the Biomedical Research and Research Training Program (CFDA 93.859), supports research to investigate the phase behavior of proteins in crowded cellular environments. The $441,108 award, spanning from Sep 2024 to Aug 2027, will enable researchers at Louisiana State University to: 1) Study the effects of molecular crowding on the phase transition of model protein/polymer systems; 2) Characterize the physical properties of the resulting phase-separated protein/polymer complexes; 3) Measure the conformation of individual protein and polymer molecules in different crowding environments; and 4) Probe the effects of crowding on protein-protein and protein-polymer interactions. The research aims to enhance the understanding of how the crowded conditions within living cells impact protein conformation and intermolecular interactions, which regulate the formation, function, and fate of biomolecular condensates. This work is expected to lay the groundwork for a comprehensive understanding of protein phase behavior in crowded cellular environments at the molecular level.

Description

Abstract
Current research proposes protein phase separation as a key mechanism underlying the formation of liquid-like biomolecular condensates, which play an integral role in numerous cellular processes and age-related disorders. The interior of a living cell is a highly crowded environment, therefore, to fully comprehend the phase behaviors and biological functions of proteins, IT is critical to consider the densely populated environment of cells, where proteins coexist with a wide variety of molecules possessing diverse physical and chemical properties. To this end, researchers have utilized various molecules as crowding agents to study protein phase behavior in this context. While the effects of crowding on proteins have been studied to some extent, many open questions remain to be addressed. The long-term goal of the proposed research is to unravel the mechanism underlying the phase separation of proteins in living cells. Our previous research explored the impact of two types of crowding agents on a model protein/polymer system, revealing that they lead to distinct phase-separated complexes due to their different effects on individual protein and polymer molecules. Therefore, based on the previous results, our central hypothesis is that the observed macroscopic crowding phenomena are directly linked to how the crowding agents affect the conformation and behavior of individual protein and polymer molecules at the molecular level. The overall objectives of this study are to enhance our understanding of the changes in conformation and intermolecular interactions that regulate protein phase behavior in crowded environments, and how these changes impact the properties of the phase separated proteins. The central hypothesis and objectives of this application will be tested and attained by pursuing four specific aims: 1) investigate the effects of crowing on the phase transition of a model protein/polymer system; 2) characterize the physical properties of the phase separated protein/polymer complexes; 3) measure the conformation of individual protein and polymer molecules in different crowding environments; 4) probe the effects of crowding on the protein- protein and protein-polymer interactions. The proposed research is anticipated to have a significant positive impact, as a detailed understanding on the protein phase behavior in crowded environments will shed light on the formation, function, and fate of biomolecular condensates. The contribution is significant because IT marks the first step in a series of investigations expected to lead to a comprehensive understanding of protein phase behavior in crowded environments at the molecular level.

Quick answers

Who received award R15GM154243?

R15GM154243 was awarded to Louisiana State University by National Institute of General Medical Sciences (National Institutes of Health) on September 20, 2024.

How much is award R15GM154243 worth?

$441,108 has been obligated on R15GM154243.

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