# A rapid test for protein–DNA interactions

**Authors:** Casey J Toft, Holly M Radford, Alanna E Sorenson, Patrick M Schaeffer

PMC · DOI: 10.1093/nar/gkag142 · Nucleic Acids Research · 2026-02-18

## TL;DR

A new rapid test called R-PNAI-T detects protein-DNA interactions quickly and without equipment, making it useful for various biological studies.

## Contribution

The R-PNAI-T assay introduces a fast, instrument-free method for detecting protein-DNA interactions with high sensitivity and versatility.

## Key findings

- The R-PNAI-T detects protein-DNA complexes in about 15 minutes using a dipstick format.
- It achieved a detection sensitivity of ~0.7 fmol with the Escherichia coli Tus protein.
- The assay works in complex biological samples like human serum and bacterial lysates.

## Abstract

The characterization of protein–DNA interactions underpinning fundamental biological processes requires methods that are laborious and time-consuming. Here, we introduce a rapid and instrument-free assay leveraging on GFP-tagged proteins and the lateral flow assay principle to examine protein–DNA interactions. The rapid protein–DNA interaction test (R-PNAI-T) detects complexes using a dipstick in ∼15 min. Validation of the R-PNAI-T with bacterial proteins involved in replication and transcription demonstrated its applicability for diverse protein–DNA interactions, achieving a remarkable detection sensitivity of ∼0.7 fmol with the Escherichia coli Tus protein. Analysis of these protein interactions with their specific target DNA sequences highlighted the capability of the R-PNAI-T to discern subtle differences in affinity, providing valuable comparative data. The R-PNAI-T is robust, retaining functionality in human serum and bacterial lysates. The assay showed tolerance towards biotin contaminants, expanding its use for quality control in protein purification processes and tracking complexes in biological samples. To demonstrate versatility, we applied the R-PNAI-T with polymerase chain reaction-amplified DNA to probe the putative origin of replication in Burkholderia pseudomallei, confirming a functional interaction between the DnaA initiator protein and the DnaA box in this bacterium. Overall, the R-PNAI-T is versatile, cost-effective, and user-friendly, offering broad applications in biological research and biotechnology.

Graphical Abstract

## Linked entities

- **Species:** Escherichia coli (taxon 562), Burkholderia pseudomallei (taxon 28450)

## Full-text entities

- **Genes:** Polr2I (RNA polymerase II subunit I) [NCBI Gene 41741] {aka CG3284, Dmel\CG3284, H5, Pol II, PolII, RNA Pol II}, Tus [NCBI Gene 8094938], LCT (lactase) [NCBI Gene 3938] {aka LAC, LPH, LPH1}, LYZ (lysozyme) [NCBI Gene 4069] {aka AMYLD5, LYZF1, LZM}, DNA-binding protein [NCBI Gene 18157783]
- **Diseases:** cancer (MESH:D009369), COVID-19 (MESH:D000086382)
- **Chemicals:** MgCl2 (MESH:D015636), FAM (MESH:C031179), gold (MESH:D006046), NaCl (MESH:D012965), acid (MESH:D000143), salt (MESH:D012492), FITC (MESH:D016650), nickel (MESH:D009532), cytosine (MESH:D003596), C (6) (MESH:C117224), biotin (MESH:D001710), oligonucleotide (MESH:D009841), LB agar (-), glycerol (MESH:D005990), sodium phosphate (MESH:C018279), fluorescein (MESH:D019793), R- (MESH:D001120), ATP (MESH:D000255), sucrose (MESH:D013395), agarose (MESH:D012685), chloramphenicol (MESH:D002701), magnesium (MESH:D008274), fluo (MESH:C097499), poly(A) (MESH:D011061)
- **Species:** Middle East respiratory syndrome-related coronavirus (no rank) [taxon 1335626], Escherichia coli (E. coli, species) [taxon 562], Saccharomyces cerevisiae (baker's yeast, species) [taxon 4932], Severe acute respiratory syndrome coronavirus 2 (no rank) [taxon 2697049], Burkholderia pseudomallei (species) [taxon 28450], Homo sapiens (human, species) [taxon 9606], Musicola paradisiaca (species) [taxon 69223], Drosophila melanogaster (fruit fly, species) [taxon 7227]
- **Cell lines:** BL21(DE3)RIPL — Mus musculus (Mouse), Hybridoma (CVCL_B7HM)

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12914326/full.md

## References

80 references — full list in the complete paper: https://tomesphere.com/paper/PMC12914326/full.md

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Source: https://tomesphere.com/paper/PMC12914326