Camilo Calvache

This paper develops bioluminescent plants that detect viral infections through spectral changes, using a protease-responsive circuit triggered by viral proteases.

The paper develops a high-throughput, quantitative bioluminescence reporter system for plant synthetic biology with improved dynamic range and application in synthetic gene circuit optimization.

The paper introduces GB_SynP, a synthetic promoter collection for controlled gene expression in plants, demonstrating its utility in analyzing enzymatic pathways.

This study shows AcrIIA4 strongly inhibits CRISPR/Cas9 and CRISPRa in plants, with tunable control via auxin-regulated fusion.