4.0 Article

Bioluminescent detection of viral surface proteins using branched multivalent protein switches

Journal

RSC CHEMICAL BIOLOGY
Volume -, Issue -, Pages -

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d3cb00164d

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Fast and reliable virus diagnostics are crucial to prevent the spread of viruses. In this study, a new sensor platform called dark-LUX is introduced for detecting viral surface proteins. The platform utilizes a general bioluminescent framework that can be modified with different binding domains to enable detection of specific viral targets. The researchers used influenza A virus surface proteins as a proof of concept and optimized various parameters to improve the sensor's performance. The modular nature of the platform allows easy adaptation to detect newly emerging viral epitopes.
Fast and reliable virus diagnostics is key to prevent the spread of viruses in populations. A hallmark of viruses is the presence of multivalent surface proteins, a property that can be harnessed to control conformational switching in sensor proteins. Here, we introduce a new sensor platform (dark-LUX) for the detection of viral surface proteins consisting of a general bioluminescent framework that can be post-translationally functionalized with separately expressed binding domains. The platform relies on (1) plug-and-play bioconjugation of different binding proteins via SpyTag/SpyCatcher technology to create branched protein structures, (2) an optimized turn-on bioluminescent switch based on complementation of the split-luciferase NanoBiT upon target binding and (3) straightforward exploration of the protein linker space. The influenza A virus (IAV) surface proteins hemagglutinin (HA) and neuraminidase (NA) were used as relevant multivalent targets to establish proof of principle and optimize relevant parameters such as linker properties, choice of target binding domains and the optimal combination of the competing NanoBiT components SmBiT and DarkBiT. The sensor framework allows rapid conjugation and exchange of various binding domains including scFvs, nanobodies and de novo designed binders for a variety of targets, including the construction of a heterobivalent switch that targets the head and stem region of hemagglutinin. The modularity of the platform thus allows straightforward optimization of binding domains and scaffold properties for existing viral targets, and is well suited to quickly adapt bioluminescent sensor proteins to effectively detect newly evolving viral epitopes. Modular virus diagnostics is key to prevent virus spread. Here, we combine state-of-the-art synthetic biology tools to create a modular bioluminescent sensor platform of branched, multivalent protein switches for detecting viral surface proteins.

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