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5OCL

Nanobody-anti-VGLUT nanobody complex

Summary for 5OCL
Entry DOI10.2210/pdb5ocl/pdb
Descriptoranti-llama nanobody, anti-vglut nanobody (3 entities in total)
Functional Keywordsnanobody, vesicular glutamate transporter, inhibitor, immune system
Biological sourceVicugna pacos (Alpaca)
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Total number of polymer chains8
Total formula weight106646.69
Authors
Dutzler, R.,Schenck, S.,Kunz, L. (deposition date: 2017-07-03, release date: 2017-07-26, Last modification date: 2024-10-23)
Primary citationSchenck, S.,Kunz, L.,Sahlender, D.,Pardon, E.,Geertsma, E.R.,Savtchouk, I.,Suzuki, T.,Neldner, Y.,Stefanic, S.,Steyaert, J.,Volterra, A.,Dutzler, R.
Generation and Characterization of Anti-VGLUT Nanobodies Acting as Inhibitors of Transport.
Biochemistry, 56:3962-3971, 2017
Cited by
PubMed Abstract: The uptake of glutamate by synaptic vesicles is mediated by vesicular glutamate transporters (VGLUTs). The central role of these transporters in excitatory neurotransmission underpins their importance as pharmacological targets. Although several compounds inhibit VGLUTs, highly specific inhibitors were so far unavailable, thus limiting applications to in vitro experiments. Besides their potential in pharmacology, specific inhibitors would also be beneficial for the elucidation of transport mechanisms. To overcome this shortage, we generated nanobodies (Nbs) by immunization of a llama with purified rat VGLUT1 and subsequent selection of binders from a phage display library. All identified Nbs recognize cytosolic epitopes, and two of the binders greatly reduced the rate of uptake of glutamate by reconstituted liposomes and subcellular fractions enriched with synaptic vesicles. These Nbs can be expressed as functional green fluorescent protein fusion proteins in the cytosol of HEK cells for intracellular applications as immunocytochemical and biochemical agents. The selected binders thus provide valuable tools for cell biology and neuroscience.
PubMed: 28731329
DOI: 10.1021/acs.biochem.7b00436
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.2 Å)
Structure validation

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