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Updated: Jan 8, 2026

From Constructs to Crystals – Towards Structure Determination of β-barrel Outer Membrane Proteins
Published on: July 4, 2016
From gatekeepers to mitochondrial mischief: how bacterial outer membrane proteins crash the host cell party
Paloma Osset-Trenor1,2,3, Markus Proft2,3, Amparo Pascual-Ahuir1
1Grupo de Ingeniería Biomolecular y Biosensores, Centro de Investigación e Innovación en Bioingeniería Ci2B, Universitat Politècnica de València, Ciudad Politécnica de la Innovación, Edificio 8B, Camino de Vera s/n, 46022 Valencia, Spain.
Abstract:
Gram-negative bacteria are equipped with a unique cell envelope structure that includes an outer membrane populated by diverse outer membrane proteins (OMPs). These OMPs are not only essential for bacterial survival, mediating critical functions such as nutrient transport, antibiotic resistance, and structural integrity, but they also play pivotal roles as virulence factors during host-pathogen interactions. Recent research highlights the ability of OMPs to manipulate host cellular processes, often targeting mitochondria to induce cell death or modulate immune responses. This review explores the multifunctional roles of bacterial OMPs, emphasizing their structural features, biogenesis, and pathogenic mechanisms. Furthermore, it delves into how bacterial OMPs exploit host cell machinery, particularly mitochondria, to promote infection, as well as their potential as targets for innovative antimicrobial strategies. Specifically, this review focuses on β-barrel OMPs that reach host mitochondria, detailing their delivery routes and mechanisms of organelle manipulation, while excluding non-β-barrel toxins and secretion-system effectors, to provide a defined perspective on mitochondria-targeting OMP virulence mechanisms.
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