Searcharxiv⌕ Search

arXiv subjects

Troy Timmerman

Publications and source records attributed to Troy Timmerman.

2 recordsLinked to original sources

Building Barricades: Red-Teaming Agentic Biosynthesis Planning

The rapid democratization of biotechnology, enhanced by large language models (LLMs) and agentic software, is eroding longstanding barriers that have limited biosynthesis planning to experts. We present BioBulbul, an agentic system that couples LLMs with open-source biodesign tools for retrobiosynthesis, enzyme selection, gene cluster design, and DNA assembly planning. Using simple natural language prompts, BioBulbul autonomously generates plausible biosynthesis pathways and corresponding gene cluster sequences for several known small molecule toxins, demonstrating that non-experts could feasibly access them using an agentic system. Our red-teaming experiments confirm the technical viability of LLM-driven toxin biosynthesis while highlighting three principal barriers: scarcity of open-source biodesign tools, limited structured enzymatic reaction data, and the complexity of many small molecule toxin pathways. We argue that these barriers are likely to diminish within a decade, expanding the biological threat landscape. To mitigate emerging risks, we recommend expanding DNA synthesis screening to include chokepoint enzymes, extending chemical supplier controls to precursor compounds, establishing continuous AI-assisted threat surveillance pipelines, and developing robust LLM guardrails. Coordinated investment across government, industry, and AI developers is essential to safeguard against the misuse of agentic biosynthesis planning.

q-bio.OT↗

FAPS: A Fast Platform for Protein Structureomics Analysis

Protein quantification and analysis are well-accepted approaches for biomarker discovery but are limited to identification without structural information. High-throughput omics data (i.e., genomics, transcriptomics, and proteomics) have become pervasive in cancer biology studies and reach well beyond more specialized areas such as metabolomics, epigenomics, pharmacogenomics, and interact-omics. However, large-scale analysis based on the structure of the biomolecules, namely structure-omics, is still underexplored due to a lack of handy tools. In response, we developed the Fast Analysis of Protein Structure (FAPS) database, a platform designed to advance quantitative proteomics to structure-omics analysis, which significantly shortens large-scale structure-omics from weeks to seconds. FAPS can serve as a new protein secondary structure database, providing a centralized and functional database for both simulated and experimentally determined bioinformatics statistics relating to secondary structure. Stored data is generated both through the structure simulation, currently SWISS-MODEL and AlphaFold, performed by high-performance computers, and the pre-existing UniProt database. FAPS provides user-friendly features that create a straightforward and effective way of accessing accurate data on the proportion of secondary structure in different protein chains, providing a fast numerical and visual reference for protein structure calculations and analysis. FAPS is accessible through http://fapsdb.org.

q-bio.QM↗