bioRxivBioinformaticsPreprint
The Virtual Lab: AI Agents Design New SARS-CoV-2 Nanobodies with Experimental Validation
Kyle SwansoniD, Wesley C. H. WuiD, Nash L. Bulaong, John E. PakiD, James ZouiD
Abstract
Science frequently benefits from teams of interdisciplinary researchers. However, most scientists dont have access to experts from multiple fields. Fortunately, large language models (LLMs) have recently shown an impressive ability to aid researchers across diverse domains by answering scientific questions. Here, we expand the capabilities of LLMs for science by introducing the Virtual Lab, an AI-human research collaboration to perform sophisticated, interdisciplinary science research. The Virtual Lab consists of an LLM principal investigator agent guiding a team of LLM agents with different scientific backgrounds (e.g., a chemist agent, a computer scientist agent, a critic agent), with a human researcher providing high-level feedback. We design the Virtual Lab to conduct scientific research through a series of team meetings, where all the agents discuss a scientific agenda, and individual meetings, where an agent accomplishes a specific task. We demonstrate the power of the Virtual Lab by applying it to design nanobody binders to recent variants of SARS-CoV-2, which is a challenging, open-ended research problem that requires reasoning across diverse fields from biology to computer science. The Virtual Lab creates a novel computational nanobody design pipeline that incorporates ESM, AlphaFold-Multimer, and Rosetta and designs 92 new nanobodies. Experimental validation of those designs reveals a range of functional nanobodies with promising binding profiles across SARS-CoV-2 variants. In particular, two new nanobodies exhibit improved binding to the recent JN.1 or KP.3 variants of SARS-CoV-2 while maintaining strong binding to the ancestral viral spike protein, suggesting exciting candidates for further investigation. This demonstrates the ability of the Virtual Lab to rapidly make impactful, real-world scientific discovery.
Abstract summary
Claude Opus 5.5 · xhigh effort · 18 Oct 2026 · from the abstract · CC BY-NC 4.0
Role-specialised LLM agents under an LLM principal investigator, with light human steering, assembled an ESM/AlphaFold-Multimer/Rosetta pipeline and designed 92 SARS-CoV-2 nanobodies; two bound recent variants better.
Interdisciplinary teams are out of reach for most labs, and language models have so far mainly answered scientific questions rather than driven a project end to end. The Virtual Lab organises several role-playing LLM agents into meetings under a human's high-level feedback, and checks the output with wet-lab binding results instead of benchmark scores alone.
Key results
ClaimedThe agent team put together a computational nanobody design pipeline built on ESM, AlphaFold-Multimer and Rosetta, and produced 92 candidate designs.
92 new nanobodies against recent SARS-CoV-2 variants; the abstract describes neither the pipeline steps, the filtering criteria, nor which model backed the agents. · Abstract
SuggestedExperimental testing of the designs found functional nanobodies with binding across SARS-CoV-2 variants.
Reported as a range of binding profiles, with no hit rate out of 92, no affinities and no assay named in the abstract. · Abstract
SuggestedTwo designs improved binding to the JN.1 or KP.3 variant while still binding the ancestral spike protein.
Stated as improved binding to a recent variant with strong binding retained to ancestral spike; no affinity values or comparator nanobodies are given. · Abstract
Methods, data and reproducibility
An LLM principal investigator agent directs role-playing LLM agents (chemist, computer scientist, critic) through team meetings that set the agenda and individual meetings for single tasks, with a human giving high-level feedback. Applied to nanobody design, the agents specified a pipeline around ESM, AlphaFold-Multimer and Rosetta whose outputs were tested experimentally.
- computationally designed nanobody binders to recent SARS-CoV-2 variants, characterised experimentally for binding · SARS-CoV-2 (virus) · n = 92 nanobodies designed
- Methods & tools
- Virtual Lab, ESM, AlphaFold-Multimer, Rosetta
- Reproducibility gaps
- The abstract names no repository, no underlying language model or version, no prompts and no sequence deposition for the 92 designs.
Limitations (2)
- No affinities, assay details or success rate among the 92 designs are reported, so how many were functional and how strongly cannot be judged from the abstract. · noted in this summary
- A single application with no control arm: the abstract reports no comparison against the same design pipeline run without the agent team, or against existing nanobodies. · noted in this summary
Read this if you are weighing multi-agent LLM workflows for real projects, or want a case where agent-specified binder design was carried through to wet-lab validation.
- Citations
- 56
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