Modelling biological modularity with CellML

被引:29
作者
Cooling, M. T. [1 ]
Hunter, P. [1 ]
Crampin, E. J. [1 ]
机构
[1] Univ Auckland, Auckland Bioengn Inst, Auckland 1, New Zealand
基金
英国惠康基金;
关键词
D O I
10.1049/iet-syb:20070020
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
In recent years advances in the construction of mathematical models of biological systems have yielded an array of valuable constructs. The authors seek to provide a 'leading practice' method for implementing modularised kinetic mass-action models in order to obtain a number of advantages in model construction, validation and derived insights. The authors advocate the consideration of 'accounting cycles' or 'chains' to define 'functional' components and the separate consideration of 'messenger' components for mobile or diffusive molecular species. From a conceptual modularisation the authors illustrate, with an example drawn from signal transduction, a component-based formulation in the model exchange format cellular modelling markup language (CellML) 1.1 - demonstrating loose coupling between functionally-focused reusable components. Finally, the authors discuss the dilemmas associated with modelling protein-to-protein interactions, and the vision for using future CellML enhancements to resolve potential duplications when combining independently developed models.
引用
收藏
页码:73 / 79
页数:7
相关论文
共 13 条
[1]   Biological networks: The tinkerer as an engineer [J].
Alon, U .
SCIENCE, 2003, 301 (5641) :1866-1867
[2]  
Alon U, 2007, INTRO SYSTEMS BIOL D
[3]   Emergent properties of networks of biological signaling pathways [J].
Bhalla, US ;
Iyengar, R .
SCIENCE, 1999, 283 (5400) :381-387
[4]   Modeling hypertrophic IP3 transients in the cardiac myocyte [J].
Cooling, Michael ;
Hunter, Peter ;
Crampin, Edmund J. .
BIOPHYSICAL JOURNAL, 2007, 93 (10) :3421-3433
[5]   From molecular to modular cell biology [J].
Hartwell, LH ;
Hopfield, JJ ;
Leibler, S ;
Murray, AW .
NATURE, 1999, 402 (6761) :C47-C52
[6]   Integration from proteins to organs: the Physiome Project [J].
Hunter, PJ ;
Borg, TK .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2003, 4 (03) :237-243
[7]   Systems biology: A brief overview [J].
Kitano, H .
SCIENCE, 2002, 295 (5560) :1662-1664
[8]   Minimum information requested in the annotation of biochemical models (MIRIAM) [J].
Le Novère, N ;
Finney, A ;
Hucka, M ;
Bhalla, US ;
Campagne, F ;
Collado-Vides, J ;
Crampin, EJ ;
Halstead, M ;
Klipp, E ;
Mendes, P ;
Nielsen, P ;
Sauro, H ;
Shapiro, B ;
Snoep, JL ;
Spence, HD ;
Wanner, BL .
NATURE BIOTECHNOLOGY, 2005, 23 (12) :1509-1515
[9]   CeIIML: its future, present and past [J].
Lloyd, CM ;
Halstead, MDB ;
Nielsen, PF .
PROGRESS IN BIOPHYSICS & MOLECULAR BIOLOGY, 2004, 85 (2-3) :433-450
[10]   A signal transduction pathway model prototype I: From agonist to cellular endpoint [J].
Lukas, TJ .
BIOPHYSICAL JOURNAL, 2004, 87 (03) :1406-1416