Sanchez Colline, Ramirez Andrea, Hodgson Louis
Gruss-Lipper Biophotonics Center, Albert Einstein College of Medicine, Bronx, New York, USA.
Department of Molecular Pharmacology, Albert Einstein College of Medicine, Bronx, New York, USA.
J Microsc. 2025 May;298(2):123-184. doi: 10.1111/jmi.13270. Epub 2024 Feb 15.
Genetically encoded, fluorescent protein (FP)-based Förster resonance energy transfer (FRET) biosensors are microscopy imaging tools tailored for the precise monitoring and detection of molecular dynamics within subcellular microenvironments. They are characterised by their ability to provide an outstanding combination of spatial and temporal resolutions in live-cell microscopy. In this review, we begin by tracing back on the historical development of genetically encoded FP labelling for detection in live cells, which lead us to the development of early biosensors and finally to the engineering of single-chain FRET-based biosensors that have become the state-of-the-art today. Ultimately, this review delves into the fundamental principles of FRET and the design strategies underpinning FRET-based biosensors, discusses their diverse applications and addresses the distinct challenges associated with their implementation. We place particular emphasis on single-chain FRET biosensors for the Rho family of guanosine triphosphate hydrolases (GTPases), pointing to their historical role in driving our understanding of the molecular dynamics of this important class of signalling proteins and revealing the intricate relationships and regulatory mechanisms that comprise Rho GTPase biology in living cells.
基于基因编码荧光蛋白(FP)的荧光共振能量转移(FRET)生物传感器是用于精确监测和检测亚细胞微环境中分子动力学的显微镜成像工具。它们的特点是能够在活细胞显微镜中提供出色的空间和时间分辨率组合。在本综述中,我们首先追溯基因编码FP标记在活细胞中检测的历史发展,这使我们发展出早期生物传感器,最终发展出基于单链FRET的生物传感器,这些传感器已成为当今的先进技术。最终,本综述深入探讨了FRET的基本原理以及基于FRET的生物传感器的设计策略,讨论了它们的各种应用,并解决了与它们的实施相关的独特挑战。我们特别强调针对鸟苷三磷酸水解酶(GTPases)的Rho家族的单链FRET生物传感器,指出它们在推动我们对这一重要信号蛋白类别的分子动力学理解方面的历史作用,并揭示了构成活细胞中Rho GTPase生物学的复杂关系和调控机制。