| Literature DB >> 31242429 |
Oriol Ros1, Yvrick Zagar1, Solène Ribes1, Sarah Baudet1, Karine Loulier1, Sandrine Couvet1, Delphine Ladarre2, Alain Aghaie3, Alice Louail1, Christine Petit3, Yves Mechulam4, Zsolt Lenkei5, Xavier Nicol6.
Abstract
cGMP is critical to a variety of cellular processes, but the available tools to interfere with endogenous cGMP lack cellular and subcellular specificity. We introduce SponGee, a genetically encoded chelator of this cyclic nucleotide that enables in vitro and in vivo manipulations in single cells and in biochemically defined subcellular compartments. SponGee buffers physiological changes in cGMP concentration in various model systems while not affecting cAMP signals. We provide proof-of-concept strategies by using this tool to highlight the role of cGMP signaling in vivo and in discrete subcellular domains. SponGee enables the investigation of local cGMP signals in vivo and paves the way for therapeutic strategies that prevent downstream signaling activation.Entities:
Keywords: (T)hPDE5(VV); FRET; PKG; axon guidance; cGMP buffer; genetically encoded; lipid grafts; neuronal migration; single cell pharmacology; subcellular compartment
Year: 2019 PMID: 31242429 DOI: 10.1016/j.celrep.2019.05.102
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423