用基于现象学的半物理模型描述了哺乳动物分泌途径中蛋白质的流动

IF 3.7 3区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Santiago Benavides-López , Laura M. Muñoz-Echeverri , Mauricio A. Trujillo-Roldán , Norma A. Valdez-Cruz
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引用次数: 0

摘要

在本研究中,我们使用基于现象学的半物理模型(PBSM)方法建立了蛋白质在分泌途径中的运输模型。该模型代表了蛋白质沿哺乳动物分泌途径细胞器的大量流动,并考虑了Ras GTPase家族循环在控制囊泡涂层组装、途径细胞器之间v-SNARE的循环以及由于囊泡在细胞器之间的恒定流动而导致的内质网和高尔基复合体体积之间的动态平衡中所起的作用。我们整合了来自人类、仓鼠和猴子细胞的文献动力学数据,以进行模型验证。该模型描述了管腔和膜蛋白的大量流动,遵循细胞器内水平的均匀混合假设和质量作用定律原理,在定量水平上揭示了分泌途径的信息。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The flow of proteins through the mammalian secretory pathway described by a phenomenological-based semi-physical model
In the present study, we developed a model for the transport of proteins across the secretory pathway using the Phenomenological Based Semi-Physical Model (PBSM) methodology. The model represents the bulk flow of proteins along the organelles of the mammalian secretory pathway and works considering the role played by the Ras GTPase family cycles in the control of the vesicle coat assembly, the recycle of v-SNARE between the organelles of the pathway, and the dynamical equilibrium between the endoplasmic reticulum and the Golgi complex volumes due to the constant flow of vesicle between organelles. We integrate literature kinetic data from human, hamster, and monkey cells for model validation. The model describes the bulk flow of luminal and membrane proteins, following the well-mixing assumption at the intra-organelle level and the mass action law principle, revealing information on the secretory pathway at a quantitative level.
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来源期刊
Biochemical Engineering Journal
Biochemical Engineering Journal 工程技术-工程:化工
CiteScore
7.10
自引率
5.10%
发文量
380
审稿时长
34 days
期刊介绍: The Biochemical Engineering Journal aims to promote progress in the crucial chemical engineering aspects of the development of biological processes associated with everything from raw materials preparation to product recovery relevant to industries as diverse as medical/healthcare, industrial biotechnology, and environmental biotechnology. The Journal welcomes full length original research papers, short communications, and review papers* in the following research fields: Biocatalysis (enzyme or microbial) and biotransformations, including immobilized biocatalyst preparation and kinetics Biosensors and Biodevices including biofabrication and novel fuel cell development Bioseparations including scale-up and protein refolding/renaturation Environmental Bioengineering including bioconversion, bioremediation, and microbial fuel cells Bioreactor Systems including characterization, optimization and scale-up Bioresources and Biorefinery Engineering including biomass conversion, biofuels, bioenergy, and optimization Industrial Biotechnology including specialty chemicals, platform chemicals and neutraceuticals Biomaterials and Tissue Engineering including bioartificial organs, cell encapsulation, and controlled release Cell Culture Engineering (plant, animal or insect cells) including viral vectors, monoclonal antibodies, recombinant proteins, vaccines, and secondary metabolites Cell Therapies and Stem Cells including pluripotent, mesenchymal and hematopoietic stem cells; immunotherapies; tissue-specific differentiation; and cryopreservation Metabolic Engineering, Systems and Synthetic Biology including OMICS, bioinformatics, in silico biology, and metabolic flux analysis Protein Engineering including enzyme engineering and directed evolution.
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