In order to improve the sensitivity and specificity of the diagnosis of Parkinson 's disease ( PD ), we selected three biomarkers, namely amyloid Aβ42, neurofilament light chain ( NF-L ), and α-synuclein ( α-syn ). On this basis, we designed the following composite parts, and overexpressed the corresponding three proteins in E.coli by means of genetic engineering. The accuracy of the obtained proteins was verified by ELISA, which can lay a foundation for the acquisition of specific antibodies and the construction of early screening kits. See the following table for detailed component composition. (Table 1).

Table1.The parts Collection
Part Number Part Name Part Type Description
BBa_K613000 lac promoter basic part Regulatory
BBa_K3521000 T7 promoter basic part Regulatory
BBa_K3521002 T7 terminator basic part Terminator
BBa_K3521004 pET28a-backbone basic part Plasmid_Backbone
BBa_K3822002 mCherry basic part Reporter
BBa_K5533000 NF-L basic part Coding
BBa_K5533001 Aβ42 basic part Coding
BBa_K5533002 α-syn basic part Coding
BBa_K5533003 pET28a-NF-L composite part Plasmid
BBa_K5533004 pET28a-NF-L-mCherry composite part Plasmid
BBa_K5533005 pET28a-Aβ42 composite part Plasmid
BBa_K5533006 pET28a-Aβ42-mCherry composite part Plasmid
BBa_K5533007 pET28a-α-syn composite part Plasmid
BBa_K5533008 pET28a-α-syn-mCherry composite part Plasmid