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本文引用的文献

1
Identifying parameter regions for multistationarity.确定多稳态的参数区域。
PLoS Comput Biol. 2017 Oct 3;13(10):e1005751. doi: 10.1371/journal.pcbi.1005751. eCollection 2017 Oct.
2
Intermediates and Generic Convergence to Equilibria.
Bull Math Biol. 2017 Jul;79(7):1662-1686. doi: 10.1007/s11538-017-0303-4. Epub 2017 Jun 15.
3
An all-encompassing global convergence result for processive multisite phosphorylation systems.关于持续性多位点磷酸化系统的一个全面的全局收敛结果。
Math Biosci. 2017 Sep;291:1-9. doi: 10.1016/j.mbs.2017.05.006. Epub 2017 Jun 29.
4
Numerical algebraic geometry for model selection and its application to the life sciences.用于模型选择的数值代数几何及其在生命科学中的应用。
J R Soc Interface. 2016 Oct;13(123). doi: 10.1098/rsif.2016.0256.
5
Intermediates, catalysts, persistence, and boundary steady states.中间体、催化剂、持久性和边界稳态。
J Math Biol. 2017 Mar;74(4):887-932. doi: 10.1007/s00285-016-1046-9. Epub 2016 Aug 1.
6
Long-term dynamics of multisite phosphorylation.多位点磷酸化的长期动力学
Mol Biol Cell. 2016 Jul 15;27(14):2331-40. doi: 10.1091/mbc.E16-03-0137. Epub 2016 May 25.
7
Graphical reduction of reaction networks by linear elimination of species.通过线性消除物种对反应网络进行图形简化。
J Math Biol. 2017 Jan;74(1-2):195-237. doi: 10.1007/s00285-016-1028-y. Epub 2016 May 24.
8
Algebraic Systems Biology: A Case Study for the Wnt Pathway.代数系统生物学:Wnt信号通路的一个案例研究
Bull Math Biol. 2016 Jan;78(1):21-51. doi: 10.1007/s11538-015-0125-1. Epub 2015 Dec 8.
9
Mixed mechanisms of multi-site phosphorylation.多位点磷酸化的混合机制
J R Soc Interface. 2015 Jun 6;12(107). doi: 10.1098/rsif.2014.1405.
10
MAPK's networks and their capacity for multistationarity due to toric steady states.丝裂原活化蛋白激酶(MAPK)网络及其由于环面稳态而产生的多稳态能力。
Math Biosci. 2015 Apr;262:125-37. doi: 10.1016/j.mbs.2014.12.010. Epub 2015 Jan 30.

翻译后修饰系统的动力学:最新进展与未来方向。

Dynamics of Posttranslational Modification Systems: Recent Progress and Future Directions.

机构信息

Department of Life Science Engineering, HTW Berlin, Berlin, Germany.

Department of Mathematics, Texas A&M University, College Station Texas, Texas.

出版信息

Biophys J. 2018 Feb 6;114(3):507-515. doi: 10.1016/j.bpj.2017.11.3787.

DOI:10.1016/j.bpj.2017.11.3787
PMID:29414696
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5985040/
Abstract

Posttranslational modification of proteins is important for signal transduction, and hence significant effort has gone toward understanding how posttranslational modification networks process information. This involves, on the theory side, analyzing the dynamical systems arising from such networks. Which networks are, for instance, bistable? Which networks admit sustained oscillations? Which parameter values enable such behaviors? In this Biophysical Perspective, we highlight recent progress in this area and point out some important future directions. Along the way, we summarize several techniques for analyzing general networks, such as eliminating variables to obtain steady-state parameterizations, and harnessing results on how incorporating intermediates affects dynamics.

摘要

蛋白质的翻译后修饰对于信号转导至关重要,因此人们付出了巨大努力来理解翻译后修饰网络是如何处理信息的。从理论角度来看,这涉及分析由此类网络产生的动态系统。例如,哪些网络是双稳态的?哪些网络允许持续振荡?哪些参数值能实现这些行为?在这篇《生物物理展望》中,我们重点介绍了该领域的最新进展,并指出了一些重要的未来方向。在此过程中,我们总结了几种分析一般网络的技术,比如消除变量以获得稳态参数化,以及利用关于纳入中间体如何影响动力学的结果。