Transport between im/mobile fractions shapes the speed and profile of cargo distribution in neurons.

IF 2.4 Q3 BIOPHYSICS
Biophysical reports Pub Date : 2022-10-20 eCollection Date: 2022-12-14 DOI:10.1016/j.bpr.2022.100082
Adriano A Bellotti, Jonathan G Murphy, Timothy S O'Leary, Dax A Hoffman
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引用次数: 0

Abstract

Neuronal function requires continuous distribution of ion channels and other proteins throughout large cell morphologies. Protein distribution is complicated by immobilization of freely diffusing subunits such as on lipid rafts or in postsynaptic densities. Here, we infer rates of immobilization for the voltage-gated potassium channel Kv4.2. Fluorescence recovery after photobleaching quantifies protein diffusion kinetics, typically reported as a recovery rate and mobile fraction. We show that, implicit in the fluorescence recovery, are rates of particle transfer between mobile and immobile fractions (im/mobilization). We performed photobleaching of fluorescein-tagged ion channel Kv4.2-sGFP2 in over 450 dendrites of rat hippocampal cells. Using mass-action models, we infer rates of Kv4.2-sGFP2 im/mobilization. Using a realistic neuron morphology, we show how these rates shape the speed and profile of subunit distribution. The experimental protocol and model inference introduced here is widely applicable to other cargo and experimental systems.

Abstract Image

Abstract Image

Abstract Image

im/mobile fractions之间的运输塑造了神经元中货物分布的速度和轮廓。
神经元的功能需要离子通道和其他蛋白质在大细胞形态中的连续分布。自由扩散的亚基如脂筏或突触后密度的固定使蛋白质分布变得复杂。在这里,我们推断电压门控钾通道Kv4.2的固定率。光漂白后的荧光恢复量化了蛋白质扩散动力学,通常以回收率和移动分数报道。我们表明,隐含在荧光恢复,是粒子转移率之间的移动和不移动的部分(im/动员)。我们对450多个大鼠海马细胞树突中荧光素标记的离子通道Kv4.2-sGFP2进行了光漂白。使用质量-作用模型,我们推断Kv4.2-sGFP2 im/动员率。利用一个真实的神经元形态,我们展示了这些速率如何塑造亚单位分布的速度和轮廓。本文介绍的实验方案和模型推理可广泛适用于其他货物和实验系统。
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
Biophysical reports
Biophysical reports Biophysics
CiteScore
2.40
自引率
0.00%
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审稿时长
75 days
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