Structural characterization of two nanobodies targeting the ligand-binding pocket of human Arc

Godoy Munoz, J. M.; Neset, L.; Markusson, S.; Weber, S.; Krokengen, O. C.; Sutinen, A.; Christakou, E.; Lopez Moreno, A. J.; Bramham, C.; Kursula, P.

doi:10.1101/2023.09.06.556498

bioRxiv · 10.1101/2023.09.06.556498

Structural characterization of two nanobodies targeting the ligand-binding pocket of human Arc

Godoy Munoz, J. M.·Neset, L.·Markusson, S.·Weber, S.·Krokengen, O. C.·Sutinen, A.·Christakou, E.·Lopez Moreno, A. J.·Bramham, C.·Kursula, P.

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Abstract

The activity-regulated cytoskeleton-associated protein (Arc) is a complex regulator of synaptic plasticity in glutamatergic neurons. Understanding its molecular function is key to elucidate the neurobiology of memory and learning, stress regulation, and multiple neurological and psychiatric diseases. The recent development of anti-Arc nanobodies has promoted the characterization of the molecular structure and function of Arc. This study aimed to validate two anti-Arc nanobodies, E5 and H11, as selective modulators of the human Arc N-lobe (Arc-NL), a domain that mediates several molecular functions of Arc through its peptide ligand binding site. The structural characteristics of recombinant Arc-NL-nanobody complexes were solved at atomic resolution using X-ray crystallography. The structures revealed that both anti-Arc nanobodies specifically bind to the multi-peptide binding site of Arc-NL. Isothermal titration calorimetry showed that the Arc-NL-nanobody interactions occur at nanomolar affinity, and that the nanobodies can displace a TARP{gamma}2-derived peptide from the Arc-NL binding site. Thus, both anti-Arc-NL nanobodies can be used in vitro as competitive inhibitors of endogenous Arc ligands. Differences in the CDR3 loops between the two nanobodies indicate that the spectrum of short linear motifs recognized by the Arc-NL should be expanded. We provide a robust biochemical background to support the use of anti-Arc nanobodies in attempts to target Arc-dependent synaptic plasticity. Function-blocking anti-Arc nanobodies could eventually help unravel the complex neurobiology of synaptic plasticity and help diagnose and treat Arc-associated synaptic disorders.

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Godoy Munoz, J. M., Neset, L., Markusson, S., Weber, S., Krokengen, O. C., Sutinen, A., Christakou, E., Lopez Moreno, A. J., Bramham, C., Kursula, P.. 2023-09-06. Structural characterization of two nanobodies targeting the ligand-binding pocket of human Arc. https://doi.org/10.1101/2023.09.06.556498

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