In the present opinion article we highlight evidence from different laboratories to drive the attention of the scientific community on the role played by endo-lysosomal Two-Pore Channels (TPCs) in viral infection. In particular, cross linking our recent data and existing literature, we focus on evidence indicating that virus intracellular pathway could be targeted by a novel occurring TPCs inhibitor, the flavonoid Naringenin. A conceptual framework is presented for considering such a strategy as a promising approach to limit the infection mediated by the novel coronavirus SARS-CoV-2. Our hypothesis offers a perspective on a novel molecular target, TPCs, which could be exploited for a pharmacological blockade of SARS-CoV-2 infectivity.
Could the Inhibition of Endo-Lysosomal Two-Pore Channels (TPCs) by the Natural Flavonoid Naringenin Represent an Option to Fight SARS-CoV-2 Infection?
Carpaneto Armando
2020
Abstract
In the present opinion article we highlight evidence from different laboratories to drive the attention of the scientific community on the role played by endo-lysosomal Two-Pore Channels (TPCs) in viral infection. In particular, cross linking our recent data and existing literature, we focus on evidence indicating that virus intracellular pathway could be targeted by a novel occurring TPCs inhibitor, the flavonoid Naringenin. A conceptual framework is presented for considering such a strategy as a promising approach to limit the infection mediated by the novel coronavirus SARS-CoV-2. Our hypothesis offers a perspective on a novel molecular target, TPCs, which could be exploited for a pharmacological blockade of SARS-CoV-2 infectivity.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.
