Author: Haljasmägi, Liis; Remm, Anu; Rumm, Anna Pauliina; Krassohhina, Ekaterina; Sein, Hanna; Tamm, Anu; Kisand, Kai; Peterson, Pärt
Title: LIPS method for the detection of SARSâ€CoVâ€2 antibodies to spike and nucleocapsid proteins Cord-id: nn7itiys Document date: 2020_7_6
ID: nn7itiys
Snippet: Profiling antibodies to SARSâ€CoVâ€2 can help to assess potential immune response after COVIDâ€19 disease. Luciferase IP system (LIPS) assay is a sensitive method for quantitative detection of antibodies to antigens in their native conformation. We here describe LIPS to detect antibody responses to SARSâ€CoVâ€2 spike (S) and nucleocapsid (N) proteins in COVIDâ€19 patients. The antibodies targeted both S and N fragments and gave a high assay sensitivity by identifying 26 out of 26 COVIDâ€1
Document: Profiling antibodies to SARSâ€CoVâ€2 can help to assess potential immune response after COVIDâ€19 disease. Luciferase IP system (LIPS) assay is a sensitive method for quantitative detection of antibodies to antigens in their native conformation. We here describe LIPS to detect antibody responses to SARSâ€CoVâ€2 spike (S) and nucleocapsid (N) proteins in COVIDâ€19 patients. The antibodies targeted both S and N fragments and gave a high assay sensitivity by identifying 26 out of 26 COVIDâ€19 patients with N antigen or with three protein fragments when combined into a single reaction. The assay correlated well with ELISA method and was specific to COVIDâ€19 as we saw no reactivity among uninfected healthy controls. Our results show that LIPS is a rapid and measurable method to screen antibody responses against SARSâ€CoVâ€2 antigens.
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