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Diagnostic TR-FRET assays for detection of antibodies in patient samples.
Yue, Hong; Nowak, Radoslaw P; Overwijn, Daan; Payne, N Connor; Fischinger, Stephanie; Atyeo, Caroline; Lam, Evan C; St Denis, Kerri; Brais, Lauren K; Konishi, Yoshinobu; Sklavenitis-Pistofidis, Romanos; Baden, Lindsey R; Nilles, Eric J; Karlson, Elizabeth W; Yu, Xu G; Li, Jonathan Z; Woolley, Ann E; Ghobrial, Irene M; Meyerhardt, Jeffrey A; Balazs, Alejandro B; Alter, Galit; Mazitschek, Ralph; Fischer, Eric S.
  • Yue H; Department of Cancer Biology, Dana-Farber Cancer Institute, Boston, MA 02215, USA.
  • Nowak RP; Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Boston, MA 02115, USA.
  • Overwijn D; Department of Cancer Biology, Dana-Farber Cancer Institute, Boston, MA 02215, USA.
  • Payne NC; Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Boston, MA 02115, USA.
  • Fischinger S; Department of Cancer Biology, Dana-Farber Cancer Institute, Boston, MA 02215, USA.
  • Atyeo C; Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Boston, MA 02115, USA.
  • Lam EC; Department of Chemistry & Chemical Biology, Harvard University, Cambridge, MA 02138, USA.
  • St Denis K; Center for Systems Biology, Massachusetts General Hospital (MGH), Boston, MA 02114, USA.
  • Brais LK; Ragon Institute of MGH, Massachusetts Institute of Technology (MIT), and Harvard, Cambridge, MA 02139, USA.
  • Konishi Y; Ragon Institute of MGH, Massachusetts Institute of Technology (MIT), and Harvard, Cambridge, MA 02139, USA.
  • Sklavenitis-Pistofidis R; Ragon Institute of MGH, Massachusetts Institute of Technology (MIT), and Harvard, Cambridge, MA 02139, USA.
  • Baden LR; Ragon Institute of MGH, Massachusetts Institute of Technology (MIT), and Harvard, Cambridge, MA 02139, USA.
  • Nilles EJ; Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA 02215, USA.
  • Karlson EW; Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA 02215, USA.
  • Yu XG; Broad Institute of MIT and Harvard, Cambridge, MA 02142, USA.
  • Li JZ; Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA 02215, USA.
  • Woolley AE; Broad Institute of MIT and Harvard, Cambridge, MA 02142, USA.
  • Ghobrial IM; Division of Infectious Diseases, Brigham and Women's Hospital, Boston, MA 02115, USA.
  • Meyerhardt JA; Department of Emergency Medicine, Brigham and Women's Hospital, Boston, MA 02115, USA.
  • Balazs AB; Department of Medicine, Brigham and Women's Hospital, Boston, MA 02115, USA.
  • Alter G; Ragon Institute of MGH, Massachusetts Institute of Technology (MIT), and Harvard, Cambridge, MA 02139, USA.
  • Mazitschek R; Division of Infectious Diseases, Brigham and Women's Hospital, Boston, MA 02115, USA.
  • Fischer ES; Division of Infectious Diseases, Brigham and Women's Hospital, Boston, MA 02115, USA.
Cell Rep Methods ; 3(3): 100421, 2023 Mar 27.
Article in English | MEDLINE | ID: covidwho-2246639
ABSTRACT
Serological assays are important diagnostic tools for surveying exposure to the pathogen, monitoring immune response post vaccination, and managing spread of the infectious agent among the population. Current serological laboratory assays are often limited because they require the use of specialized laboratory technology and/or work with a limited number of sample types. Here, we evaluate an alternative by developing time-resolved Förster resonance energy transfer (TR-FRET) homogeneous assays that exhibited exceptional versatility, scalability, and sensitivity and outperformed or matched currently used strategies in terms of sensitivity, specificity, and precision. We validated the performance of the assays measuring total immunoglobulin G (IgG) levels; antibodies against severe acute respiratory syndrome coronavirus (SARS-CoV) or Middle Eastern respiratory syndrome (MERS)-CoV spike (S) protein; and SARS-CoV-2 S and nucleocapsid (N) proteins and applied it to several large sample sets and real-world applications. We further established a TR-FRET-based ACE2-S competition assay to assess the neutralization propensity of the antibodies. Overall, these TR-FRET-based serological assays can be rapidly extended to other antigens and are compatible with commonly used plate readers.
Keywords

Full text: Available Collection: International databases Database: MEDLINE Type of study: Diagnostic study / Experimental Studies / Observational study / Prognostic study Topics: Vaccines Language: English Journal: Cell Rep Methods Year: 2023 Document Type: Article Affiliation country: J.crmeth.2023.100421

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Full text: Available Collection: International databases Database: MEDLINE Type of study: Diagnostic study / Experimental Studies / Observational study / Prognostic study Topics: Vaccines Language: English Journal: Cell Rep Methods Year: 2023 Document Type: Article Affiliation country: J.crmeth.2023.100421