Fat traffic control: S-acylation in axonal transport.

IF 3.2 3区 医学 Q2 PHARMACOLOGY & PHARMACY
Amelia H Doerksen, Nisandi N Herath, Shaun S Sanders
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引用次数: 0

Abstract

Neuronal axons serve as a conduit for the coordinated transport of essential molecular cargo between structurally and functionally distinct subcellular compartments via axonal molecular machinery. Long-distance, efficient axonal transport of membrane-bound organelles enables signal transduction and neuronal homeostasis. Efficient axonal transport is conducted by dynein and kinesin ATPase motors that use a local ATP supply from metabolic enzymes tethered to transport vesicles. Molecular motor adaptor proteins promote the processive motility and cargo selectivity of fast axonal transport. Axonal transport impairments are directly causative or associated with many neurodegenerative diseases and neuropathologies. Cargo specificity, cargo-adaptor proteins, and posttranslational modifications of cargo, adaptor proteins, microtubules, or the motor protein subunits all contribute to the precise regulation of vesicular transit. One posttranslational lipid modification that is particularly important in neurons in regulating protein trafficking, protein-protein interactions, and protein association with lipid membranes is S-acylation. Interestingly, many fast axonal transport cargos, cytoskeletal-associated proteins, motor protein subunits, and adaptors are S-acylated to modulate axonal transport. Here, we review the established regulatory role of S-acylation in fast axonal transport and provide evidence for a broader role of S-acylation in regulating the motor-cargo complex machinery, adaptor proteins, and metabolic enzymes from low-throughput studies and S-acyl-proteomic data sets. We propose that S-acylation regulates fast axonal transport and vesicular motility through localization of the proteins required for the motile cargo-complex machinery and relate how perturbed S-acylation contributes to transport impairments in neurological disorders. SIGNIFICANCE STATEMENT: This review investigates the regulatory role of S-acylation in fast axonal transport and its connection to neurological diseases, with a focus on the emerging connections between S-acylation and the molecular motors, adaptor proteins, and metabolic enzymes that make up the trafficking machinery.

脂肪运输控制:轴突运输中的s -酰化。
神经元轴突通过轴突分子机制在结构和功能不同的亚细胞间协调运输必需的分子货物。膜结合细胞器的远距离、高效的轴突运输使信号转导和神经元稳态成为可能。有效的轴突运输是由动力蛋白和动力蛋白ATP酶马达进行的,它们利用连接在运输囊泡上的代谢酶提供的局部ATP供应。分子马达接头蛋白促进快速轴突运输的过程运动性和货物选择性。轴突运输损伤是许多神经退行性疾病和神经病理的直接病因或相关因素。货物特异性、货物衔接蛋白和货物、衔接蛋白、微管或马达蛋白亚基的翻译后修饰都有助于精确调节水泡运输。一种翻译后的脂质修饰在神经元中调节蛋白质运输、蛋白质-蛋白质相互作用和蛋白质与脂质膜的关联方面特别重要,即s -酰化。有趣的是,许多快速轴突运输货物、细胞骨架相关蛋白、运动蛋白亚基和接头都被s酰化以调节轴突运输。在这里,我们回顾了s -酰化在快速轴索运输中的调节作用,并从低通量研究和s -酰化蛋白质组学数据集提供了s -酰化在调节发动机-货物复合物机械、衔接蛋白和代谢酶方面的更广泛作用的证据。我们提出s -酰化调节快速轴突运输和水泡运动通过定位所需的蛋白质的运动货物-复杂机制,并涉及如何干扰s -酰化有助于运输障碍在神经系统疾病。意义声明:本综述研究了s -酰化在快速轴突运输中的调节作用及其与神经系统疾病的联系,重点关注了s -酰化与构成运输机制的分子马达、接头蛋白和代谢酶之间的新联系。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Molecular Pharmacology
Molecular Pharmacology 医学-药学
CiteScore
7.20
自引率
2.80%
发文量
50
审稿时长
3-6 weeks
期刊介绍: Molecular Pharmacology publishes findings derived from the application of innovative structural biology, biochemistry, biophysics, physiology, genetics, and molecular biology to basic pharmacological problems that provide mechanistic insights that are broadly important for the fields of pharmacology and toxicology. Relevant topics include: Molecular Signaling / Mechanism of Drug Action Chemical Biology / Drug Discovery Structure of Drug-Receptor Complex Systems Analysis of Drug Action Drug Transport / Metabolism
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