Abstract NanoLuc® luciferase (NLuc) and its complementation technologies, including the NanoBiT® LgBiT/HiBiT system, are widely applied in functional biology because of their exceptional brightness, broad dynamic range, and suitability for monitoring real-time cellular processes. Despite their versatility, NLuc-based reporters emit primarily at a single, blue-shifted wavelength (∼460 nm), restricting their use in multiplexed assays where independent spectral channels are required. To overcome this limitation, we developed NanoPrism™ luciferases, engineered NLuc variants that employ highly efficient intramolecular energy transfer to red-shift the emission. Building on BRET-based strategies, we inserted circularly permuted NLuc or LgBiT into a surface loop of HaloTag®, enabling optimal positioning to covalently bound fluorophores and achieving exceptional BRET efficiency (∼90%). By pairing these red-shifted NanoPrism™ reporters with unmodified NLuc® or NanoBiT®, we created a robust two-color bioluminescent platform with strong signal intensities and 100 nm spectral separation. This dual-channel system allows simultaneous monitoring of two proteins or cellular events, such as targeted protein degradation, signaling dynamics, or internal control measurements - in real time within a single experimental context. Citation Format: Juliano Alves, Karilyn Porter, Mike Killoran, Robin Hurst, Mark Klein, Debayan De Bakshi, Rahele Esmatpour, James J. Cali, Thomas Machleidt, Rachel F. Ohana, Hicham Zegzouti. Two-color bioluminescence analyses pairing NanoLuc® and red-shifted NanoPrism™ luciferases abstract. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 1 (Regular Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(7 Suppl):Abstract nr 288.
Alves et al. (Fri,) studied this question.