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Title:
High-throughput multiplexed serology via the mass-spectrometric analysis of isotopically barcoded beads | Nature Biomedical Engineering
Description:
In serology, each sample is typically tested individually, one antigen at a time. This is costly and time consuming. Serology techniques should ideally allow recurrent measurements in parallel in small sample volumes and be inexpensive and fast. Here we show that mass cytometry can be used to scale up multiplexed serology testing by leveraging polystyrene beads uniformly loaded with combinations of stable isotopes. We generated 18,480 unique isotopically barcoded beads to simultaneously detect, in a single tube with 924 serum samples, the levels of immunoglobulins G and M against 19 proteins from SARS-CoV-2 (a total of 36,960 tests in 400 nl of sample volume and 30 μl of reaction volume). As a rapid, high-throughput and cost-effective technique, serology by mass cytometry may contribute to the effective management of public health emergencies originating from infectious diseases. Mass cytometry can be used to scale up multiplexed serology testing, as shown for the simultaneous detection of antibody levels against multiple SARS-CoV-2 proteins in hundreds of serum samples.
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nature portfolio privacy policy wild-type sars-cov-2 trimer advertising anti-sars-cov-2 igg antibodies detect anti-sars-cov-2 antibodies elisa kits powerful tools nature 595 nature social media confirmed sars-cov-2-positive tests sars-cov-2 spike trimer biomedical engineering mrna-1273 sars-cov-2 vaccine undiagnosed sars-cov-2 seropositivity solutions reprints anti-sars-cov-2 antibodies quantify sars-cov-2 rna wild-type trimer quantified sars-cov-2 omicron sublineages full sars-cov-2 spike sars-cov-2 variant biology sars-cov-2 spike s1 confirmed sars-cov-2 infection sars-cov-2 infected households sars-cov-2 antibody profiles positive sars-cov-2 tests human anti-spike s1 multiplexed bead-based immunoassays ucsf-affiliated health facility single-cell deconvolution algorithm enzyme-linked immunosorbent assay secondary anti-igg antibody engineering luminescent biosensors ultrasensitive high-resolution profiling isotope-conjugated biotinylated proteins high-throughput serology testing pid2023-152897oa-i00 funded government-sponsored serology surveillance xavier rovira-clav� isotope-based serology assay streptavidin-coated polystyrene beads anti-igg magnetic beads magnetic anti-igg beads high-throughput multiplexed serology bead-based serology assays sars-cov-2 infection mass cytometry-based serology
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headline:High-throughput multiplexed serology via the mass-spectrometric analysis of isotopically barcoded beads
description:In serology, each sample is typically tested individually, one antigen at a time. This is costly and time consuming. Serology techniques should ideally allow recurrent measurements in parallel in small sample volumes and be inexpensive and fast. Here we show that mass cytometry can be used to scale up multiplexed serology testing by leveraging polystyrene beads uniformly loaded with combinations of stable isotopes. We generated 18,480 unique isotopically barcoded beads to simultaneously detect, in a single tube with 924 serum samples, the levels of immunoglobulins G and M against 19 proteins from SARS-CoV-2 (a total of 36,960 tests in 400ânl of sample volume and 30âμl of reaction volume). As a rapid, high-throughput and cost-effective technique, serology by mass cytometry may contribute to the effective management of public health emergencies originating from infectious diseases. Mass cytometry can be used to scale up multiplexed serology testing, as shown for the simultaneous detection of antibody levels against multiple SARS-CoV-2 proteins in hundreds of serum samples.
datePublished:2025-02-12T00:00:00Z
dateModified:2025-02-12T00:00:00Z
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ELISA
Mass spectrometry
Prognostic markers
SARS-CoV-2
Biomedicine
general
Biomedical Engineering/Biotechnology
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headline:High-throughput multiplexed serology via the mass-spectrometric analysis of isotopically barcoded beads
description:In serology, each sample is typically tested individually, one antigen at a time. This is costly and time consuming. Serology techniques should ideally allow recurrent measurements in parallel in small sample volumes and be inexpensive and fast. Here we show that mass cytometry can be used to scale up multiplexed serology testing by leveraging polystyrene beads uniformly loaded with combinations of stable isotopes. We generated 18,480 unique isotopically barcoded beads to simultaneously detect, in a single tube with 924 serum samples, the levels of immunoglobulins G and M against 19 proteins from SARS-CoV-2 (a total of 36,960 tests in 400ânl of sample volume and 30âμl of reaction volume). As a rapid, high-throughput and cost-effective technique, serology by mass cytometry may contribute to the effective management of public health emergencies originating from infectious diseases. Mass cytometry can be used to scale up multiplexed serology testing, as shown for the simultaneous detection of antibody levels against multiple SARS-CoV-2 proteins in hundreds of serum samples.
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Mass spectrometry
Prognostic markers
SARS-CoV-2
Biomedicine
general
Biomedical Engineering/Biotechnology
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