Constrained Multistate Sequence Design for Nucleic Acid Reaction Pathway EngineeringConstrained Multistate Sequence Design for Nucleic Acid Reaction Pathway Engineering

被引:74
|
作者
Wolfe, Brian R. [1 ]
Porubsky, Nicholas J. [2 ]
Zadeh, Joseph N. [1 ]
Dirks, Robert M. [1 ]
Pierce, Niles A. [1 ,3 ,4 ]
机构
[1] CALTECH, Div Biol & Biol Engn, Pasadena, CA 91125 USA
[2] CALTECH, Div Chem & Chem Engn, Pasadena, CA 91125 USA
[3] CALTECH, Div Engn & Appl Sci, Pasadena, CA 91125 USA
[4] Univ Oxford, Inst Mol Med, Oxford OX3 9DS, England
基金
美国国家科学基金会;
关键词
HYBRIDIZATION CHAIN-REACTION; RNA SECONDARY STRUCTURE; DNA STRAND DISPLACEMENT; THERMODYNAMIC PROPERTIES; GENE-EXPRESSION; LOGIC-CIRCUITS; ALGORITHM; SHAPE; AMPLIFICATION; REGULATORS;
D O I
10.1021/jacs.6b12693
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We describe a framework for designing the sequences of multiple nucleic acid strands intended to hybridize in solution via a prescribed reaction pathway. Sequence design is formulated as a multistate optimization problem using a set of target test tubes to represent reactant, intermediate, and product states of the system, as well as to model crosstalk between components. Each target test tube contains a set of desired "on -target" complexes, each with a target secondary structure and target concentration, and a set of undesired "off -target" complexes, each with vanishing target concentration. Optimization of the equilibrium ensemble properties of the target test tubes implements both a positive design paradigm, explicitly designing for on pathway elementary steps, and a negative design paradigm, explicitly designing against off -pathway crosstalk. Sequence design is performed subject to diverse user -specified sequence constraints including composition constraints, complementarity constraints, pattern prevention constraints, and biological constraints. Constrained multistate sequence design facilitates nucleic acid reaction pathway engineering for diverse applications in molecular programming and synthetic biology. Design jobs can be run online via the NUPACK web application.
引用
收藏
页码:3134 / 3144
页数:11
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