Controllability Analysis and Control Synthesis for the Ribosome Flow Model

被引:3
|
作者
Zarai, Yoram [1 ]
Margaliot, Michael [2 ,3 ]
Sontag, Eduardo D. [4 ,5 ]
Tuller, Tamir [1 ,3 ]
机构
[1] Tel Aviv Univ, Dept Biomed Engn, IL-69978 Tel Aviv, Israel
[2] Tel Aviv Univ, Sch Elect Engn, IL-69978 Tel Aviv, Israel
[3] Tel Aviv Univ, Sagol Sch Neurosci, IL-69978 Tel Aviv, Israel
[4] Rutgers State Univ, Dept Math, Piscataway, NJ 08854 USA
[5] Rutgers State Univ, Canc Ctr New Jersey, Piscataway, NJ 08854 USA
关键词
Systems biology; synthetic biology; gene translation; ribosomal density profile; controllability; asymptotic controllability; accessibility; control-affine systems; Lie-algebra; control synthesis; ribosome flow model; MESSENGER-RNA TRANSLATION; GENE-EXPRESSION; PROTEIN-SYNTHESIS; POLYMERASE; EFFICIENCY; INITIATION; MECHANISM; YEAST;
D O I
10.1109/TCBB.2017.2707420
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The ribosomal density along different parts of the coding regions of the mRNA molecule affects various fundamental intracellular phenomena including: protein production rates, global ribosome allocation and organismal fitness, ribosomal drop off, co-translational protein folding, mRNA degradation, and more. Thus, regulating translation in order to obtain a desired ribosomal profile along the mRNA molecule is an important biological problem. We study this problem by using a dynamical model for mRNA translation, called the ribosome flow model (RFM). In the RFM, the mRNA molecule is modeled as an ordered chain of n sites. The RFM includes n state-variables describing the ribosomal density profile along the mRNA molecule, and the transition rates from each site to the next are controlled by n + 1 positive constants. To study the problem of controlling the density profile, we consider some or all of the transition rates as time-varying controls. We consider the following problem: given an initial and a desired ribosomal density profile in the RFM, determine the time-varying values of the transition rates that steer the system to the desired density profile, if they exist. More specifically, we consider two control problems. In the first, all transition rates can be regulated separately, and the goal is to steer the ribosomal density profile and the protein production rate from a given initial value to a desired value. In the second problem, one or more transition rates are jointly regulated by a single scalar control, and the goal is to steer the production rate to a desired value within a certain set of feasible values. In the first case, we show that the system is controllable, i.e., the control is powerful enough to steer the system to any desired value in finite time, and provide simple closed-form expressions for constant positive control functions (or transition rates) that asymptotically steer the system to the desired value. In the second case, we show that the system is controllable, and provide a simple algorithm for determining the constant positive control value that asymptotically steers the system to the desired value. We discuss some of the biological implications of these results.
引用
收藏
页码:1351 / 1364
页数:14
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