PO.ET02.07 · 实验与分子治疗

配对 NanoLuc® 与红移 NanoPrism™ 荧光素酶的双色生物发光分析

Two-color bioluminescence analyses pairing NanoLuc® and red-shifted NanoPrism™ luciferases​

海报缩略图:配对 NanoLuc® 与红移 NanoPrism™ 荧光素酶的双色生物发光分析
编号 288 展板 6 时间 4/19 02:00–05:00 区域 Section 13 主讲 Juliano Alves, PhD
分会场 Innovative Therapeutic Modalities and Translational Platforms
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作者与单位 Authors & Affiliations

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

Promega Corporation, Madison, WI

摘要 Abstract

中文摘要
NanoLuc® 荧光素酶(NLuc)及其互补技术,包括 NanoBiT® LgBiT/HiBiT 系统,因其卓越的亮度、宽广的动态范围以及适于监测实时细胞过程的特性,被广泛应用于功能生物学。尽管用途多样,基于 NLuc 的报告基因主要在单一、蓝移波长(约 460 nm)处发光,限制了其在需要独立光谱通道的多重检测中的应用。为克服这一局限,我们开发了 NanoPrism™ 荧光素酶,这是一种经过改造的 NLuc 变体,利用高效的分子内能量转移使发射光谱红移。基于 BRET 策略,我们将环化重排的 NLuc 或 LgBiT 插入 HaloTag® 表面环内,使其相对于共价结合的荧光团处于最佳位置,从而实现卓越的 BRET 效率(约 90%)。通过将这些红移的 NanoPrism™ 报告基因与未经修饰的 NLuc® 或 NanoBiT® 配对,我们构建了一个稳健的双色生物发光平台,具有强信号强度和 >100 nm 的光谱分离。该双通道系统可在单一实验条件下实时同步监测两种蛋白或细胞事件,例如靶向蛋白降解、信号动力学或内参测量。
查看英文原文 English 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.
利益披露 Disclosure
J. Alves, Promega Corporation Employment. K. Porter, Promega Corporation Employment. M. Killoran, Promega Corporation Employment. R. Hurst, Promega Corporation Employment. M. Klein, Promega Corporation Employment. D. De Bakshi, Promega Corporation Employment. R. Esmatpour, Promega Corporation Employment. J. J. Cali, Promega Corporation Employment. T. Machleidt, Promega Corporation Employment. R. F. Ohana, Promega Corporation Employment. H. Zegzouti, Promega Corporation Employment.

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