Simulation and real-time monitoring of polymerase chain reaction for its higher efficiency

被引:12
作者
Lee, JY
Lim, HW
Yoo, SI
Zhang, BT
Park, TH
机构
[1] Seoul Natl Univ, Sch Chem & Biol Engn, Seoul 151744, South Korea
[2] Seoul Natl Univ, Sch Comp Sci & Engn, Seoul 151744, South Korea
关键词
bioreactions; DNA; enzyme inactivation; modeling; polymerase chain reaction (PCR); plateau;
D O I
10.1016/j.bej.2005.02.023
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
Polymerase chain reaction (PCR) is an important molecular biological tool for the amplification of nucleic acids. PCR process can be divided into three phases according to the amplification rate: exponential, quasi-linear, and plateau. We investigated the Cause of the plateau phenomenon through real-time monitoring of the amplification profile and computerized Simulation. Possible limiting components, Such its Taq DNA polymerase, primer pair, and dNTPs were added during quasi-linear phase, after which the differences in the amplification profiles were monitored. Modeling and computerized simulations were performed to look into the complex mechanism of the reactions, such as renaturation of templates during temperature transition from denaturation to annealing step and effective enzyme concentration profiles within the cycle progress. The decrease of effective polymerase concentration clue to heat inactivation and product accumulation caused the PCR plateau. Addition of polymerase during the quasi-linear phase could increase the final product amount; however, the PCR process still reached the plateau phase in spite of polymerase addition. Simulation results suggest that renaturation of templates before competitive annealing reaction and decrease of effective enzyme concentration by non-specific binding of polymerase to double-stranded DNA is the main contribution to plateau forming. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:109 / 118
页数:10
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