Soft constraints-based multiobjective framework for flux balance analysis

被引:33
作者
Nagrath, Deepak [3 ]
Avila-Elchiver, Marco [1 ,2 ,4 ]
Berthiaume, Francois [1 ,2 ,6 ]
Tilles, Arno W. [1 ,2 ]
Messac, Achille [5 ]
Yarmush, Martin L. [1 ,2 ,6 ]
机构
[1] Harvard Univ, Massachusetts Gen Hosp, Sch Med, Ctr Engn Med Surg Serv, Boston, MA 02114 USA
[2] Shriners Hosp Children, Boston, MA 02114 USA
[3] Rice Univ, Dept Chem & Biomol Engn, Houston, TX 77005 USA
[4] MIT, Harvard Mit Div Hlth Sci & Technol, Cambridge, MA 02139 USA
[5] Rensselaer Polytech Inst, Dept Mech Engn, Troy, NY USA
[6] Rutgers State Univ, Dept Biomed Engn, Piscataway, NJ 08854 USA
基金
美国国家卫生研究院;
关键词
Bioartificial liver; Hepatocytes/linear physical programming; Metabolic networks; Multiobjective optimization; Pareto optimality; OPTIMIZATION; IDENTIFICATION; HEPATOCYTES; CELLS; METABOLISM; GLUTAMINE; SELECTION; INSULIN; ENERGY; EMU;
D O I
10.1016/j.ymben.2010.05.003
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The current state of the art for linear optimization in Flux Balance Analysis has been limited to single objective functions. Since mammalian systems perform various functions, a multiobjective approach is needed when seeking optimal flux distributions in these systems. In most of the available multiobjective optimization methods, there is a lack of understanding of when to use a particular objective, and how to combine and/or prioritize mutually competing objectives to achieve a truly optimal solution. To address these limitations we developed a soft constraints based linear physical programming-based flux balance analysis (LPPFBA) framework to obtain a multiobjective optimal solutions. The developed framework was first applied to compute a set of multiobjective optimal solutions for various pairs of objectives relevant to hepatocyte function (urea secretion, albumin, NADPH, and glutathione syntheses) in bioartificial liver systems. Next, simultaneous analysis of the optimal solutions for three objectives was carried out. Further, this framework was utilized to obtain true optimal conditions to improve the hepatic functions in a simulated bioartificial liver system. The combined quantitative and visualization framework of LPPFBA is applicable to any large-scale metabolic network system, including those derived by genomic analyses. (C) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:429 / 445
页数:17
相关论文
共 30 条
[1]   Metabolic flux analysis in a nonstationary system:: Fed-batch fermentation of a high yielding strain of E. coli producing 1,3-propanediol [J].
Antoniewicz, Maciek R. ;
Kraynie, David F. ;
Laffend, Lisa A. ;
Gonzalez-Lergier, Joanna ;
Kelleher, Joanne K. ;
Stephanopoulos, Gregory .
METABOLIC ENGINEERING, 2007, 9 (03) :277-292
[2]   Elementary metabolite units (EMU): A novel framework for modeling isotopic distributions [J].
Antoniewicz, Maciek R. ;
Kelleher, Joanne K. ;
Stephanopoulos, Gregory .
METABOLIC ENGINEERING, 2007, 9 (01) :68-86
[3]   Quantitative effects of thermal injury and insulin on the metabolism of the skeletal muscle using the perfused rat hindquarter preparation [J].
Banta, S ;
Yokoyama, T ;
Berthiaume, F ;
Yarmush, ML .
BIOTECHNOLOGY AND BIOENGINEERING, 2004, 88 (05) :613-629
[4]   Effect of extracellular matrix topology on cell structure, function, and physiological responsiveness: Hepatocytes cultured in a sandwich configuration [J].
Berthiaume, F ;
Moghe, PV ;
Toner, M ;
Yarmush, ML .
FASEB JOURNAL, 1996, 10 (13) :1471-1484
[5]   Optimization-based framework for inferring and testing hypothesized metabolic objective functions [J].
Burgard, AP ;
Maranas, CD .
BIOTECHNOLOGY AND BIOENGINEERING, 2003, 82 (06) :670-677
[6]   Metabolic flux analysis of cultured hepatocytes exposed to plasma [J].
Chan, C ;
Berthiaume, F ;
Lee, K ;
Yarmush, ML .
BIOTECHNOLOGY AND BIOENGINEERING, 2003, 81 (01) :33-49
[7]   Metabolic flux analysis of hepatocyte function in hormone- and amino acid-supplemented plasma [J].
Chan, C ;
Berthiaume, F ;
Lee, K ;
Yarmush, ML .
METABOLIC ENGINEERING, 2003, 5 (01) :1-15
[8]   Application of multivariate analysis to optimize function of cultured hepatocytes [J].
Chan, C ;
Hwang, D ;
Stephanopoulos, GN ;
Yarmush, ML ;
Stephanopoulos, G .
BIOTECHNOLOGY PROGRESS, 2003, 19 (02) :580-598
[9]   Metabolic pre-conditioning of cultured cells in physiological levels of insulin: Generating resistance to the lipid-accumulating effects of plasma in hepatocytes [J].
Chan, C ;
Berthiaume, F ;
Washizu, J ;
Toner, M ;
Yarmush, ML .
BIOTECHNOLOGY AND BIOENGINEERING, 2002, 78 (07) :753-760
[10]   Development of a metabolic network design and optimization framework incorporating implementation constraints: A succinate production case study [J].
Cox, SJ ;
Levanon, SS ;
Sanchez, A ;
Lin, H ;
Peercy, B ;
Bennett, GN ;
San, KY .
METABOLIC ENGINEERING, 2006, 8 (01) :46-57