Molecular Architecture of Contactin-associated Protein-like 2 (CNTNAP2) and its Interaction with Contactin 2 (CNTN2).
Research paper by
Zhuoyang Z Lu, M V V V Sekhar MV Reddy, Jianfang J Liu, Ana A Kalichava, Jiankang J Liu, Lei L Zhang, Fang F Chen, Yun Y Wang, Luis Marcelo F LM Holthauzen, Mark A MA White, Suchithra S Seshadrinathan, Xiaoying X Zhong, Gang G Ren, Gabby G Rudenko
Contactin-associated protein-like 2 (CNTNAP2) is a large multi-domain neuronal adhesion molecule implicated in a number of neurological disorders, including epilepsy, schizophrenia, autistic spectrum disorder (ASD), intellectual disability, and language delay. We reveal here by electron microscopy that the architecture of CNTNAP2 is composed of a large, medium, and small lobe that flex with respect to each other. Using epitope labeling and fragments, we assign the F58C, L1, and L2 domains to the large lobe, the FBG and L3 domains to the middle lobe, and the L4 domain to the small lobe of the CNTNAP2 molecular envelop. Our data reveal that CNTNAP2 has a very different architecture compared to neurexin 1alpha, a fellow member of the neurexin superfamily and a prototype, suggesting that CNTNAP2 uses a different strategy to integrate into the synaptic protein network. We show that the ectodomains of CNTNAP2 and contactin 2 (CNTN2) bind directly and specifically, with low nanomolar affinity. We show further that mutations in CNTNAP2 implicated in ASD are not segregated, but are distributed over the whole ectodomain. The molecular shape and dimensions of CNTNAP2 place constraints on how CNTNAP2 integrates in the cleft of axo-glial and neuronal contact sites and how it functions as an organizing and adhesive molecule.