Publications by authors named "Zane Fink"

Article Synopsis
  • - PepSeq is an advanced technique for conducting comprehensive proteomic assays using DNA-barcoded peptides, allowing researchers to study the interactions and specificities of proteins in a highly multiplexed manner.
  • - The process involves synthesizing a library of peptide/DNA conjugates from a small serum or plasma sample, enabling epitope-level analysis of antibodies and providing insights into pathogen exposure history.
  • - The protocol consists of two key parts: designing and creating the DNA-barcoded peptide libraries and employing these libraries for high-throughput serological testing, with analysis supported by user-friendly software tools for efficient data handling.
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The SARS-CoV-2 proteome shares regions of conservation with endemic human coronaviruses (CoVs), but it remains unknown to what extent these may be cross-recognized by the antibody response. Here, we study cross-reactivity using a highly multiplexed peptide assay (PepSeq) to generate an epitope-resolved view of IgG reactivity across all human CoVs in both COVID-19 convalescent and negative donors. PepSeq resolves epitopes across the SARS-CoV-2 Spike and Nucleocapsid proteins that are commonly targeted in convalescent donors, including several sites also recognized in some uninfected controls.

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A high-resolution understanding of the antibody response to SARS-CoV-2 is important for the design of effective diagnostics, vaccines and therapeutics. However, SARS-CoV-2 antibody epitopes remain largely uncharacterized, and it is unknown whether and how the response may cross-react with related viruses. Here, we use a multiplexed peptide assay ('PepSeq') to generate an epitope-resolved view of reactivity across all human coronaviruses.

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