Boccaccio Anna
Institute of Biophysics, Consiglio Nazionale delle Ricerche, Genoa, Italy.
RAISE Ecosystem, Genoa, Italy.
Methods Mol Biol. 2025;2888:119-132. doi: 10.1007/978-1-0716-4318-1_9.
In recent years, the elucidation of molecular mechanisms underlying lipid scrambling has raised significant attention to its implications in various physiological processes, such as blood coagulation, viral infection, cell fusion processes, and removal of apoptotic cells. This chapter focuses on a HEK293 cell-based assay tailored to assess the lipid scrambling activity of the Ca-activated scramblases of the TMEM16/Anoctamin family. It relies on the capacity of Annexin-V to detect the presence of negatively charged lipids and, in particular, phosphatidylserine, on the extracellular surface of the plasma membrane. Although most TMEM16 scramblases, with the exception of TMEM16F, have an intracellular localization, some of them partially localize at the plasma membrane, allowing a direct functional characterization. Annexin-V-based scrambling assay offers a versatile platform for investigating the lipid scrambling properties of TMEM16 family members and their mutants associated with genetic diseases, facilitating the elucidation of their roles in cellular physiology and pathology.
近年来,对脂质翻转分子机制的阐明引发了人们对其在各种生理过程中影响的高度关注,这些生理过程包括血液凝固、病毒感染、细胞融合过程以及凋亡细胞的清除。本章重点介绍一种基于HEK293细胞的检测方法,该方法专门用于评估跨膜蛋白16/八聚体家族的钙激活翻转酶的脂质翻转活性。它依赖于膜联蛋白V检测质膜细胞外表面带负电荷脂质尤其是磷脂酰丝氨酸的能力。尽管除了跨膜蛋白16F之外,大多数跨膜蛋白16翻转酶定位于细胞内,但其中一些部分定位于质膜,从而可以进行直接的功能表征。基于膜联蛋白V的翻转检测为研究跨膜蛋白16家族成员及其与遗传疾病相关的突变体的脂质翻转特性提供了一个通用平台,有助于阐明它们在细胞生理和病理中的作用。