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量化环境敏感探针的荧光寿命响应用于测量膜流动性。

Quantifying Fluorescence Lifetime Responsiveness of Environment-Sensitive Probes for Membrane Fluidity Measurements.

机构信息

Department of Women's and Children's Health, Science for Life Laboratory, Karolinska Institutet, 17165 Solna, Sweden.

Weatherall Institute of Molecular Medicine, University of Oxford, OX39DS Oxford, United Kingdom.

出版信息

J Phys Chem B. 2024 Mar 7;128(9):2154-2167. doi: 10.1021/acs.jpcb.3c07006. Epub 2024 Feb 28.

Abstract

The structural diversity of different lipid species within the membrane defines its biophysical properties such as membrane fluidity, phase transition, curvature, charge distribution, and tension. Environment-sensitive probes, which change their spectral properties in response to their surrounding milieu, have greatly contributed to our understanding of such biophysical properties. To realize the full potential of these probes and avoid misinterpretation of their spectral responses, a detailed investigation of their fluorescence characteristics in different environments is necessary. Here, we examined the fluorescence lifetime of two newly developed membrane order probes, NR12S and NR12A, in response to alterations in their environments such as the degree of lipid saturation, cholesterol content, double bond position and configuration, and phospholipid headgroup. As a comparison, we investigated the lifetime sensitivity of the membrane tension probe Flipper in these environments. Applying fluorescence lifetime imaging microscopy (FLIM) in both model membranes and biological membranes, all probes distinguished membrane phases by lifetime but exhibited different lifetime sensitivities to varying membrane biophysical properties (e.g., cholesterol). While the lifetime of Flipper is particularly sensitive to the membrane cholesterol content, the NR12S and NR12A lifetimes are moderately sensitive to both the cholesterol content and lipid acyl chains. Moreover, all of the probes exhibit longer lifetimes at longer emission wavelengths in membranes of any complexity. This emission wavelength dependency results in varying lifetime resolutions at different spectral regions, which are highly relevant for FLIM data acquisition. Our data provide valuable insights on how to perform FLIM with these probes and highlight both their potential and limitations.

摘要

不同膜内脂质种类的结构多样性决定了其生物物理特性,如膜流动性、相变、曲率、电荷分布和张力。环境敏感探针会根据周围环境改变其光谱特性,这极大地促进了我们对这些生物物理特性的理解。为了充分发挥这些探针的潜力并避免对其光谱响应的误解,有必要详细研究它们在不同环境中的荧光特性。在这里,我们研究了两种新开发的膜有序探针 NR12S 和 NR12A 的荧光寿命,以响应其环境的变化,如脂质饱和度、胆固醇含量、双键位置和构型以及磷脂头部基团。作为比较,我们研究了膜张力探针 Flipper 在这些环境中的寿命灵敏度。通过在模型膜和生物膜中应用荧光寿命成像显微镜(FLIM),所有探针都通过寿命区分了膜相,但对不同的膜生物物理性质(如胆固醇)表现出不同的寿命灵敏度。虽然 Flipper 的寿命对膜胆固醇含量特别敏感,但 NR12S 和 NR12A 的寿命对胆固醇含量和脂质酰基链都有一定的敏感性。此外,所有探针在任何复杂性的膜中,随着发射波长的增加,寿命都会延长。这种发射波长依赖性导致在不同光谱区域的寿命分辨率不同,这对 FLIM 数据采集非常重要。我们的数据提供了有关如何使用这些探针进行 FLIM 的有价值的见解,并强调了它们的潜力和局限性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e8c/10926104/9abfa6a69a0f/jp3c07006_0001.jpg

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