Genre
Post-printDate
2021-03-23Author
Gunaratne, Gihan S.Brailoiu, Eugen
He, Shijun
UNTERWALD, ELLEN
Patel, Sandip
Slama, James T
Walseth, Timothy F.
Marchant, Jonathan S.
Group
Center for Substance Abuse Research (Temple University)Department
Neural SciencesPermanent link to this record
http://hdl.handle.net/20.500.12613/7032
Metadata
Show full item recordDOI
https://doi.org/10.1126/scisignal.abd5605Abstract
Nicotinic acid adenine dinucleotide phosphate (NAADP) is a second messenger that releases Ca2+ from acidic organelles through the activation of two-pore channels (TPCs) to regulate endolysosomal trafficking events. NAADP action is mediated by NAADP-binding protein(s) of unknown identity that confer NAADP sensitivity to TPCs. Here, we used a “clickable” NAADP-based photoprobe to isolate human NAADP-binding proteins and identified Jupiter microtubule-associated homolog 2 (JPT2) as a TPC accessory protein required for endogenous NAADP-evoked Ca2+ signaling. JPT2 was also required for the translocation of a severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) pseudovirus through the endolysosomal system. Thus, JPT2 is a component of the NAADP receptor complex that is essential for TPC-dependent Ca2+ signaling and control of coronaviral entry.Citation to related work
American Association for the Advancement of ScienceHas part
Science Signaling, Vol. 14ADA compliance
For Americans with Disabilities Act (ADA) accommodation, including help with reading this content, please contact scholarshare@temple.eduae974a485f413a2113503eed53cd6c53
http://dx.doi.org/10.34944/dspace/7013