1. Academic Validation
  2. Long-Term Monitoring of Enzymatic Activity at the Single-Organelle Level via Reversed Plasmonic Resonance Energy Transfer

Long-Term Monitoring of Enzymatic Activity at the Single-Organelle Level via Reversed Plasmonic Resonance Energy Transfer

  • ACS Nano. 2025 Oct 14;19(40):35901-35912. doi: 10.1021/acsnano.5c13054.
Dengyun Lu 1 2 He Wang 1 Yang Shi 1 Ting Pan 1 Qingsong Mei 3 Baojun Li 1 Luke P Lee 4 5 6 Hongbao Xin 1
Affiliations

Affiliations

  • 1 Guangdong Provincial Key Laboratory of Nanophotonic Manipulation, Institute of Nanophotonics, College of Physics & Optoelectronic Engineering, Jinan University, Guangzhou 511443, P. R. China.
  • 2 College of Electronic Information and Physics, Central South University of Forestry and Technology, Changsha 410004, P. R. China.
  • 3 Department of Medical Biochemistry and Molecular Biology, School of Medicine, Jinan University, Guangzhou 510632, P. R. China.
  • 4 Renal Division and Division of Engineering in Medicine, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Harvard University, Boston, Massachusetts 02115, United States.
  • 5 Department of Bioengineering and Department of Electrical Engineering and Computer Science, University of California, Berkeley, California 94720, United States.
  • 6 Institute of Quantum Biophysics, Department of Biophysics, Sungkyunkwan University, Suwon 16419, Korea.
Abstract

Observing and comprehending enzymatic activity in interorganelle communication can yield critical insights into the intricate mechanisms that govern cellular metabolism. However, real-time and long-term monitoring of enzymatic activity at the single-organelle level is challenging, especially during interorganelle communications. Here, we present an optical technique to track oxygen-dependent enzymatic activity in real-time over several hours, concentrating on endosomal-lysosomal interactions at the single-organelle level through reversed plasmonic resonance energy transfer (rPRET). We created urchin-shaped gold nanoparticles as optical nanoantennas by interfacing with resonating black hole quencher molecules to detect azoreductase in individual lysosomes, revealing differences in enzyme activity within Cancer and noncancerous cells. Upon entering the lysosome, the rPRET nanoantenna acts as a hypoxic nanoprobe, effectively detecting oxygen signals within the cell. Noninvasive optical monitoring of oxygen-related enzyme activity during prolonged endosome-lysosome interactions enables the identification of differences in enzymatic activities between intact and apoptotic cells. The rPRET nanoantenna offers a method for examining enzymatic regulation during interorganelle interactions in cellular metabolism, focusing on both single-cell and single-organelle levels.

Keywords

enzymatic activity; interorganelle interactions; molecular imaging; nanoplasmonics; reversed plasmonic resonance energy transfer.

Figures
Products