| Literature DB >> 34035500 |
Lutz Gieselmann1,2, Christoph Kreer1, Meryem Seda Ercanoglu1, Nathalie Lehnen1, Matthias Zehner1, Philipp Schommers1,2,3, Julian Potthoff1, Henning Gruell1,2, Florian Klein4,5,6.
Abstract
As exemplified by the ongoing severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) pandemic, there is a strong demand for rapid high-throughput isolation pipelines to identify potent neutralizing antibodies for prevention and therapy of infectious diseases. However, despite substantial progress and extensive efforts, the identification and production of antigen-specific antibodies remains labor- and cost-intensive. We have advanced existing concepts to develop a highly efficient high-throughput protocol with proven application for the isolation of potent antigen-specific antibodies against human immunodeficiency virus 1, hepatitis C virus, human cytomegalovirus, Middle East respiratory syndrome coronavirus, SARS-CoV-2 and Ebola virus. It is based on computationally optimized multiplex primer sets (openPrimeR), which guarantee high coverage of even highly mutated immunoglobulin gene segments as well as on optimized antibody cloning and production strategies. Here, we provide the detailed protocol, which covers all critical steps from sample collection to antibody production within 12-14 d.Entities:
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Year: 2021 PMID: 34035500 DOI: 10.1038/s41596-021-00554-w
Source DB: PubMed Journal: Nat Protoc ISSN: 1750-2799 Impact factor: 13.491