Franck Duong

This paper uses MM-TPP to show that cholesteryl hemisuccinate broadly stabilizes membrane proteins across different systems and membrane mimetics.

This paper introduces Peptergents, a detergent-free method for native membrane proteomics that preserves protein structure and function, enabling better analysis of membrane proteins and their interactions.

This paper introduces a detergent-free method using amphipathic peptides to extract and purify membrane proteins, enabling improved structural and mass spectrometry analysis.

This paper uses membrane-mimetic proteomics to show that AD-related membrane proteome changes are enriched in APP mice, and M1 receptor activation selectively affects disease-altered membrane networks.

This study compares seven membrane proteomic workflows, finding that solid-phase methods capture more total proteins while membrane mimetics enrich membrane proteins, with Peptidisc excelling in detecting dysregulated membrane proteins in diseased liver.

This study identifies YibN as a functional interactor of YidC, showing it enhances membrane protein insertion and lipid production in bacteria.

The paper introduces a method using peptidiscs to stabilize hydrophobic protein associations, enabling the production of multimeric and multispecific nanobody proteins.

This paper introduces MM-TPP, a method to map membrane protein-ligand interactions using Peptidisc and thermal proteome profiling, showing it detects specific ligand effects on ABC transporters and GPCRs better than detergent-based TPP.

This study identifies dysregulated membrane proteins in liver disease using peptidisc-based proteomics in mice, highlighting lipid metabolism and xenobiotic processing pathways.

The paper investigates the structural dynamics of SctV, a component of the Type III translocase export gate in E. coli, revealing its conformational changes and interactions with chaperones and ATPase.