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Biology subjects

Garden, P. M.

Publications and source records attributed to Garden, P. M..

2 recordsLinked to original sources

Rapid Isothermal Detection of Heavy Metals via Transcription-Factor-Gated DNA Strand Synthesis

Conventional methods for monitoring toxic heavy metals typically require sophisticated laboratory instrumentation and leave a critical gap for rapid, on-site detection. Herein we present Transcription-factor-Occluded Nick Extension or TONE, a rapid, isothermal biosensing platform for heavy metal detection that exploits allosteric transcription factor (aTF) regulation to gate DNA strand-displacement amplification. In this approach, operator sequences modified with deoxyinosine (dI) substitutions are employed. When bound by an aTF, the dI sites are shielded from cleavage by Endonuclease V. Upon exposure to target heavy metals, the aTF dissociates, permitting the enzyme to nick the DNA and trigger a strand-displacement reaction. The amplified DNA is then detected via an instrument-free lateral flow assay, delivering a visual readout within 25 minutes at room temperature. We demonstrate the utility of TONE using the TetR aTF and further adapt the assay for copper and lead detection through the transcription factors CsoR and CadC, respectively, achieving detection limits as low as 40 nM and 80 nM, respectively. TONE offers a sensitive, low-cost, and field-deployable solution for environmental monitoring and other applications requiring rapid heavy metal analysis.

synthetic biology↗

A Rapid and Modular Nanobody Assay for Plug-and-Play Antigen Detection

Rapid and portable antigen detection is essential for managing infectious diseases and responding to toxic exposures, yet current methods face significant limitations. Highly sensitive platforms like the Enzyme-Linked Immunosorbent Assay (ELISA) are time- and cost-prohibitive for point-of-need detection, while portable options like lateral flow assays (LFAs) require systemic overhauls for new targets. Furthermore, the complex infrastructure, high production costs, and extended timelines for assay development constrain manufacturing of traditional diagnostic platforms in low-resource settings. To address these challenges, we describe the Rapid and Modular Nanobody Assay (RAMONA) as a versatile antigen detection platform that leverages nanobody-coiled coil fusion proteins for modular integration with downstream readout methods. RAMONA merges the portability of LFAs with the benefits of nanobodies, such as their smaller size, improved solubility, and compatibility with cell-free protein synthesis systems, enabling on-demand biomanufacturing and rapid adaptation for diverse targets. We demonstrate assay generalizability through the detection of three distinct protein targets, robustness across various temperatures and incubation periods, and compatibility with saliva samples and cell-free synthesis. Detection occurs in under 30 minutes, with results strongly and positively correlating to ELISA data while requiring minimal resources. Moreover, RAMONA supports multiplexed detection of three antigens simultaneously using orthogonal capture probes. By overcoming several limitations of traditional immunoassays, RAMONA represents a significant advancement in rapid, adaptable, and field-deployable antigen detection technologies.

bioengineering↗