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Targeting multiprotein receptor complexes, rather than receptors directly, is a promising concept in drug discovery. This is particularly relevant to the GABA B receptor complex, which plays a prominent role in many brain functions and diseases. Here, we provide the first studies targeting a key protein–protein interaction of the GABA B receptor complex—the interaction with KCTD proteins. By employing the μSPOT technology, we first defined the GABA B receptor-binding epitope mediating the KCTD interaction. Subsequently, we developed a highly potent peptide-based inhibitor that interferes with the KCTD/GABA B receptor complex and efficiently isolates endogenous KCTD proteins from mouse brain lysates. X-ray crystallography and SEC-MALS revealed inhibitor induced oligomerization of KCTD16 into a distinct hexameric structure. Thus, we provide a template for modulating the GABA B receptor complex, revealing a fundamentally novel approach for targeting GABA B receptor-associated neuropsychiatric disorders.
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Sereikaité et al. (2019) studied this question.
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