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分子转子——用于粘度和流量检测的荧光生物传感器

Molecular rotors--fluorescent biosensors for viscosity and flow.

作者信息

Haidekker Mark A, Theodorakis Emmanuel A

机构信息

Department of Biological Engineering, University of Missouri-Columbia, Columbia, MO 65211, USA.

出版信息

Org Biomol Chem. 2007 Jun 7;5(11):1669-78. doi: 10.1039/b618415d. Epub 2007 Apr 12.

Abstract

Viscosity is a measure of the resistance of a fluid against gradients in flow (shear rate). Both flow and viscosity play an important role in all biological systems from the microscopic (e.g., cellular) to the systemic level. Many methods to measure viscosity and flow have drawbacks, such as the tedious and time-consuming measurement process, expensive instrumentation, or the restriction to bulk sample sizes. Fluorescent environment-sensitive dyes are known to show high sensitivity and high spatial and temporal resolution. Molecular rotors are a group of fluorescent molecules that form twisted intramolecular charge transfer (TICT) states upon photoexcitation and therefore exhibit two competing deexcitation pathways: fluorescence emission and non-radiative deexcitation from the TICT state. Since TICT formation is viscosity-dependent, the emission intensity of molecular rotors depends on the solvent's viscosity. Furthermore, shear-stress dependency of the emission intensity was recently described. Although the photophysical processes are widely explored, the practical application of molecular rotors as sensors for viscosity and the fluid flow introduce additional challenges. Intensity-based measurements are influenced by fluid optical properties and dye concentration, and solvent-dye interaction requires calibration of the measurement system to a specific solvent. Ratiometric dyes and measurement systems help solve these challenges. In addition, the combination of molecular rotors with specific recognition groups allows them to target specific sites, for example the cell membrane or cytoplasm. Molecular rotors are therefore emerging as new biosensors for both bulk and local microviscosity, and for flow and fluid shear stress on a microscopic scale and with real-time response.

摘要

粘度是衡量流体抵抗流动梯度(剪切速率)的能力。从微观层面(如细胞)到系统层面,流动和粘度在所有生物系统中都起着重要作用。许多测量粘度和流动的方法都存在缺点,例如测量过程繁琐且耗时、仪器昂贵,或者仅限于大体积样本。众所周知,荧光环境敏感染料具有高灵敏度以及高空间和时间分辨率。分子转子是一类荧光分子,在光激发时形成扭曲的分子内电荷转移(TICT)态,因此呈现出两种相互竞争的去激发途径:荧光发射和从TICT态的非辐射去激发。由于TICT的形成取决于粘度,分子转子的发射强度取决于溶剂的粘度。此外,最近还描述了发射强度对剪切应力的依赖性。尽管对光物理过程进行了广泛研究,但将分子转子作为粘度和流体流动传感器的实际应用带来了额外的挑战。基于强度的测量受流体光学性质和染料浓度的影响,并且溶剂 - 染料相互作用需要将测量系统校准到特定溶剂。比率型染料和测量系统有助于解决这些挑战。此外,分子转子与特定识别基团的结合使它们能够靶向特定部位,例如细胞膜或细胞质。因此,分子转子正成为用于测量大体积和局部微粘度、以及微观尺度上的流动和流体剪切应力并具有实时响应的新型生物传感器。

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