| Literature DB >> 33275650 |
Yujing Song1, Erin Sandford2, Yuzi Tian3,4, Qingtian Yin5, Andrew G Kozminski1, Shiuan-Haur Su1, Tao Cai1, Yuxuan Ye1, Meng Ting Chung1, Ryan Lindstrom2, Annika Goicochea2, Jenny Barabas2, Mary Olesnavich2, Michelle Rozwadowski6, Yongqing Li3, Hasan B Alam3, Benjamin H Singer7,8, Monalisa Ghosh2, Sung Won Choi6,8,9, Muneesh Tewari2,9,10,11, Katsuo Kurabayashi1,8,12.
Abstract
Digital protein assays have great potential to advance immunodiagnostics because of their single-molecule sensitivity, high precision, and robust measurements. However, translating digital protein assays to acute clinical care has been challenging because it requires deployment of these assays with a rapid turnaround. Herein, we present a technology platform for ultrafast digital protein biomarker detection by using single-molecule counting of immune-complex formation events at an early, pre-equilibrium state. This method, which we term "pre-equilibrium digital enzyme-linked immunosorbent assay" (PEdELISA), can quantify a multiplexed panel of protein biomarkers in 10 µL of serum within an unprecedented assay incubation time of 15 to 300 seconds over a 104 dynamic range. PEdELISA allowed us to perform rapid monitoring of protein biomarkers in patients manifesting post-chimeric antigen receptor T-cell therapy cytokine release syndrome, with ∼30-minute sample-to-answer time and a sub-picograms per mL limit of detection. The rapid, sensitive, and low-input volume biomarker quantification enabled by PEdELISA is broadly applicable to timely monitoring of acute disease, potentially enabling more personalized treatment.Entities:
Year: 2021 PMID: 33275650 PMCID: PMC8065241 DOI: 10.1182/blood.2019004399
Source DB: PubMed Journal: Blood ISSN: 0006-4971 Impact factor: 22.113