Current Methods for Detecting Cell Membrane Transient Interactions.

Current Methods for Detecting Cell Membrane Transient Interactions.
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DOI:
10.3389/fchem.2020.603259
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发表时间:
2020
影响因子:
5.5
通讯作者:
You M
You M
中科院分区:
化学3区
文献类型:
--
作者:
Bagheri Y;Ali AA;You M

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短寿命细胞膜复合物在调节细胞信号和通讯中起着关键作用。许多这些复合物是基于各种脂质和蛋白质之间的低亲和力和短暂相互作用而形成的。研究这些以前被忽视的膜瞬态相互作用的新技术已经出现。这些短暂相互作用的令人兴奋的功能已经在细胞事件中被发现,如免疫信号、宿主-病原体相互作用和癌症等疾病。在这篇综述中,我们总结了目前的实验方法,使我们能够检测和分析短寿命细胞膜蛋白-蛋白,脂质-蛋白和脂质-脂质相互作用。这些方法可以提供有关膜瞬态相互作用的强度、动力学和/或空间模式的有用信息。然而,每种方法也有其自身的局限性。我们希望这篇综述可以作为指导,帮助读者选择合适的方法来研究不同的膜运输和细胞信号事件中的膜瞬态相互作用。
Short-lived cell membrane complexes play a key role in regulating cell signaling and communication. Many of these complexes are formed based on low-affinity and transient interactions among various lipids and proteins. New techniques have emerged to study these previously overlooked membrane transient interactions. Exciting functions of these transient interactions have been discovered in cellular events such as immune signaling, host–pathogen interactions, and diseases such as cancer. In this review, we have summarized current experimental methods that allow us to detect and analyze short-lived cell membrane protein–protein, lipid–protein, and lipid–lipid interactions. These methods can provide useful information about the strengths, kinetics, and/or spatial patterns of membrane transient interactions. However, each method also has its own limitations. We hope this review can be used as a guideline to help the audience to choose proper approaches for studying membrane transient interactions in different membrane trafficking and cell signaling events.
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