Understanding complex signaling networks through models and metaphors

被引:60
作者
Bhalla, US [1 ]
机构
[1] Natl Ctr Biol Ctr, Bangalore 560065, Karnataka, India
关键词
biochemical pathways; computer simulation; logical networks; neural networks; databases; bioinformatics; INTERACTING PROTEINS; SOFTWARE ENVIRONMENT; CELL; PATHWAYS; DATABASE; MAP; ORGANIZATION; ACTIVATION; DYNAMICS; MODULES;
D O I
10.1016/S0079-6107(02)00046-9
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Signaling networks are complex both in terms of the chemical and biophysical events that underlie them, and in the sheer number of interactions. Computer models are powerful tools to deal with both aspects of complexity, but their utility goes beyond simply replicating signaling events in silicon. Their great advantage is as a tool to understanding. The completeness of the description demanded by computer models highlights gaps in knowledge. The quantitative description in models facilitates a mapping between different kinds of analysis methods for complex systems. Systems analysis methods can highlight stable states of signaling networks and describe the transitions between them. Modeling also reveals functional similarities between signaling network properties and other well-understood systems such as electronic devices and neural networks. These suggest various metaphors as a tool to understanding. Based on such descriptions, it is possible to regard signaling networks as systems that decode complex inputs in time, space and chemistry into combinatorial output patterns of signaling activity. This would provide a natural interface to the combinatorial input patterns required by genetic circuits. Thus, a combination of computer modeling methods to capture the complexity and details, and useful abstractions revealed by these models, is necessary to achieve both rigorous description as well as human understanding. (C) 2003 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:45 / 65
页数:21
相关论文
共 58 条
[1]   A quantitative analysis of the kinetics of the G2 DNA damage checkpoint system [J].
Aguda, BD .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (20) :11352-11357
[2]  
Arkin A, 1998, GENETICS, V149, P1633
[3]   BIND - The Biomolecular Interaction Network Database [J].
Bader, GD ;
Donaldson, I ;
Wolting, C ;
Ouellette, BFF ;
Pawson, T ;
Hogue, CWV .
NUCLEIC ACIDS RESEARCH, 2001, 29 (01) :242-245
[4]   Homogeneous and spatio-temporal chaos in biochemical reactions with feedback inhibition [J].
Baier, G ;
Sahle, S .
JOURNAL OF THEORETICAL BIOLOGY, 1998, 193 (02) :233-242
[5]   Strategies for the physiome project [J].
Bassingthwaighte, JB .
ANNALS OF BIOMEDICAL ENGINEERING, 2000, 28 (08) :1043-1058
[6]   Interaction with the NMDA receptor locks CaMKII in an active conformation [J].
Bayer, KU ;
De Koninck, P ;
Leonard, AS ;
Hell, JW ;
Schulman, H .
NATURE, 2001, 411 (6839) :801-805
[7]  
Bhalla US, 2001, NOVART FDN SYMP, V239, P4
[8]   MAP kinase phosphatase as a locus of flexibility in a mitogen-activated protein kinase signaling network [J].
Bhalla, US ;
Ram, PT ;
Iyengar, R .
SCIENCE, 2002, 297 (5583) :1018-1023
[9]   Biochemical signaling networks decode temporal patterns of synaptic input [J].
Bhalla, US .
JOURNAL OF COMPUTATIONAL NEUROSCIENCE, 2002, 13 (01) :49-62
[10]   Mechanisms for temporal tuning and filtering by postsynaptic signaling pathways [J].
Bhalla, US .
BIOPHYSICAL JOURNAL, 2002, 83 (02) :740-752