Pathogen Moonlighting Proteins

Moonlighting and multitasking proteins refer to proteins with two or more functions performed by a single polypeptide chain. An amazing example of the Gain of Function (GoF) phenomenon of these proteins is that 25% of the moonlighting functions of our Multitasking Proteins Database (MultitaskProtDB-...

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Detalles Bibliográficos
Autores: Franco Serrano, Luis|||0000-0002-7308-7333, Sánchez-Redondo, David, Nájar-García, Araceli, Hernández Ranzani, Sergio, Amela Abellan, Isaac, Pérez-Pons, Josep A.|||0000-0002-5062-2989, Piñol Ribas, Jaume|||0000-0002-9055-8934, Mozo-Villarias, Angel|||0000-0001-6559-7926, Cedano, Juan|||0000-0003-1380-8036, Querol Murillo, Enrique|||0000-0002-3658-3434
Tipo de recurso: artículo
Fecha de publicación:2021
País:España
Institución:Universitat Autònoma de Barcelona
Repositorio:Dipòsit Digital de Documents de la UAB
Idioma:inglés
OAI Identifier:oai:ddd.uab.cat:256445
Acceso en línea:https://ddd.uab.cat/record/256445
https://dx.doi.org/urn:doi:10.3390/microorganisms9061300
Access Level:acceso abierto
Palabra clave:Moonlighting proteins
Multitasking proteins
Microbial pathogens
Pathogen virulence factors
Vaccines
Descripción
Sumario:Moonlighting and multitasking proteins refer to proteins with two or more functions performed by a single polypeptide chain. An amazing example of the Gain of Function (GoF) phenomenon of these proteins is that 25% of the moonlighting functions of our Multitasking Proteins Database (MultitaskProtDB-II) are related to pathogen virulence activity. Moreover, they usually have a canonical function belonging to highly conserved ancestral key functions, and their moonlighting functions are often involved in inducing extracellular matrix (ECM) protein remodeling. There are three main questions in the context of moonlighting proteins in pathogen virulence: (A) Why are a high percentage of pathogen moonlighting proteins involved in virulence? (B) Why do most of the canonical functions of these moonlighting proteins belong to primary metabolism? Moreover, why are they common in many pathogen species? (C) How are these different protein sequences and structures able to bind the same set of host ECM protein targets, mainly plasminogen (PLG), and colonize host tissues? By means of an extensive bioinformatics analysis, we suggest answers and approaches to these questions. There are three main ideas derived from the work: first, moonlighting proteins are not good candidates for vaccines. Second, several motifs that might be important in the adhesion to the ECM were identified. Third, an overrepresentation of GO codes related with virulence in moonlighting proteins were seen.