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Human Coronavirus Cell Receptors Provide Challenging Therapeutic Targets.
López-Cortés, Georgina I; Palacios-Pérez, Miryam; Hernández-Aguilar, Margarita M; Veledíaz, Hannya F; José, Marco V.
Afiliação
  • López-Cortés GI; Facultad de Química, Universidad Nacional Autónoma de México (UNAM), México City C.P. 04510, Mexico.
  • Palacios-Pérez M; Theoretical Biology Group, Instituto de Investigaciones Biomédicas, Universidad Nacional Autónoma de México (UNAM), México City C.P. 04510, Mexico.
  • Hernández-Aguilar MM; Network of Researchers on the Chemical Evolution of Life (NoRCEL), Leeds LS7 3RB, UK.
  • Veledíaz HF; Theoretical Biology Group, Instituto de Investigaciones Biomédicas, Universidad Nacional Autónoma de México (UNAM), México City C.P. 04510, Mexico.
  • José MV; Network of Researchers on the Chemical Evolution of Life (NoRCEL), Leeds LS7 3RB, UK.
Vaccines (Basel) ; 11(1)2023 Jan 13.
Article em En | MEDLINE | ID: mdl-36680018
Coronaviruses interact with protein or carbohydrate receptors through their spike proteins to infect cells. Even if the known protein receptors for these viruses have no evolutionary relationships, they do share ontological commonalities that the virus might leverage to exacerbate the pathophysiology. ANPEP/CD13, DPP IV/CD26, and ACE2 are the three protein receptors that are known to be exploited by several human coronaviruses. These receptors are moonlighting enzymes involved in several physiological processes such as digestion, metabolism, and blood pressure regulation; moreover, the three proteins are expressed in kidney, intestine, endothelium, and other tissues/cell types. Here, we spot the commonalities between the three enzymes, the physiological functions of the enzymes are outlined, and how blocking either enzyme results in systemic deregulations and multi-organ failures via viral infection or therapeutic interventions is addressed. It can be difficult to pinpoint any coronavirus as the target when creating a medication to fight them, due to the multiple processes that receptors are linked to and their extensive expression.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Vaccines (Basel) Ano de publicação: 2023 Tipo de documento: Article País de afiliação: México País de publicação: Suíça

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Vaccines (Basel) Ano de publicação: 2023 Tipo de documento: Article País de afiliação: México País de publicação: Suíça