Design of a dimeric‐nanobody specific for Aß_1‐42 oligomers: the Dimeric‐DesAb‐O

Abstract Background Small, soluble oligomers, rather than mature fibrils, are the major neurotoxic agents in Alzheimer’s disease (AD). In the last few years, Aprile and co‐workers designed and purified a single‐domain antibody (sdAb), called DesAb‐O, with high specificity for Aβ 1‐42 oligomeric conformers. Recently, Cascella and co‐workers showed that DesAb‐O can selectively detect synthetic Aβ 1‐42 oligomers both in vitro and in cultured cells, neutralizing their associated neuronal dysfunction. DesAb‐O can also identify Aβ 1‐42 oligomers in the cerebrospinal fluid (CSF) of AD patients, with respect to healthy individuals, preventing cell dysfunction induced by the administration of CSFs to neuronal cells. Given the extraodinary potentialities of this nanobody, we design a dimeric‐structure of DesAb‐O, with the aim to increase its avidity and affinity for toxic Aβ 1‐42 oligomers. Method We designed the dimeric‐DesAb‐O structure by linking two DesAb‐O monomeric domains with a flexible linker region (GGGGS) 3. Once expressed and purified the protein, we characterised its molecular weight by mass spectrometry and its secondary structure by Circular Dichroism. Then, we performed an aggregation assay to monitor its ability to interfere with the Aβ 1‐42 aggregation process and a Real‐Time based ELISA assay to study its binding for Aβ 1‐42 oligomers. Result The Dimeric‐DesAb‐O is able to interfere with the Aβ 1‐42 aggregation process to a greater extent than DesAb‐O. Furthermore, the dimeric structure of DesAb‐O showed a higher specificity and affinity for Aβ 1‐42 oligomers compared to DesAb‐O. Conclusion The Dimeric‐DesAb‐O appears to be a promising tool for the future development of sdAbs‐based immunodiagnostic tests for the early diagnosis of AD.