A Versatile Synaptotagmin‐1 Nanobody Provides Perturbation‐Free Live Synaptic Imaging And Low Linkage‐Error in Super‐Resolution Microscopy

Imaging of living synapses has relied for over two decades on the overexpression of synaptic proteins fused to fluorescent reporters. This strategy alters the stoichiometry of synaptic components and ultimately affects synapse physiology. To overcome these limitations, here a nanobody is presented t...

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Published inSmall methods Vol. 7; no. 10; p. e2300218
Main Authors Queiroz Zetune Villa Real, Karine, Mougios, Nikolaos, Rehm, Ronja, Sograte‐Idrissi, Shama, Albert, László, Rahimi, Amir Mohammad, Maidorn, Manuel, Hentze, Jannik, Martínez‐Carranza, Markel, Hosseini, Hassan, Saal, Kim‐Ann, Oleksiievets, Nazar, Prigge, Matthias, Tsukanov, Roman, Stenmark, Pål, Fornasiero, Eugenio F., Opazo, Felipe
Format Journal Article
LanguageEnglish
Published Germany 01.10.2023
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ISSN2366-9608
2366-9608
DOI10.1002/smtd.202300218

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Summary:Imaging of living synapses has relied for over two decades on the overexpression of synaptic proteins fused to fluorescent reporters. This strategy alters the stoichiometry of synaptic components and ultimately affects synapse physiology. To overcome these limitations, here a nanobody is presented that binds the calcium sensor synaptotagmin‐1 (NbSyt1). This nanobody functions as an intrabody (iNbSyt1) in living neurons and is minimally invasive, leaving synaptic transmission almost unaffected, as suggested by the crystal structure of the NbSyt1 bound to Synaptotagmin‐1 and by the physiological data. Its single‐domain nature enables the generation of protein‐based fluorescent reporters, as showcased here by measuring spatially localized presynaptic Ca 2+ with a NbSyt1‐ jGCaMP8 chimera. Moreover, the small size of NbSyt1 makes it ideal for various super‐resolution imaging methods. Overall, NbSyt1 is a versatile binder that will enable imaging in cellular and molecular neuroscience with unprecedented precision across multiple spatiotemporal scales.
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ISSN:2366-9608
2366-9608
DOI:10.1002/smtd.202300218