A multi-enzyme model for pyrosequencing

被引:39
作者
Agah, A
Aghajan, M
Mashayekhi, F
Amini, S
Davis, RW
Plummer, JD
Ronaghi, M [1 ]
Griffin, PB
机构
[1] Stanford Univ, Stanford Genome Technol Ctr, Palo Alto, CA 94304 USA
[2] Stanford Univ, Ctr Integrated Syst, Palo Alto, CA 94304 USA
[3] Univ Tehran, Inst Biochem & Biophys, Tehran, Iran
关键词
D O I
10.1093/nar/gnh159
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
Pyrosequencing is a DNA sequencing technique based on sequencing-by-synthesis enabling rapid real-time sequence determination. This technique employs four enzymatic reactions in a single tube to monitor DNA synthesis. Nucleotides are added iteratively to the reaction and in case of incorporation, pyrophosphate (PPi) is released. PPi triggers a series of reactions resulting in production of light, which is proportional to the amount of DNA and number of incorporated nucleotides. Generated light is detected and recorded by a detector system in the form of a peak signal, which reflects the activity of all four enzymes in the reaction. We have developed simulations to model the kinetics of the enzymes. These simulations provide a full model for the Pyrosequencing four-enzyme system, based on which the peak height and shape can be predicted depending on the concentrations of enzymes and substrates. Simulation results are shown to be compatible with experimental data. Based on these simulations, the rate-limiting steps in the chain can be determined, and K-M and k(cat) of all four enzymes in Pyrosequencing can be calculated.
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页数:15
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共 31 条
  • [1] A NOVEL METHOD FOR NUCLEIC-ACID SEQUENCE DETERMINATION
    BAINS, W
    SMITH, GC
    [J]. JOURNAL OF THEORETICAL BIOLOGY, 1988, 135 (03) : 303 - 307
  • [2] Gene expression analysis by massively parallel signature sequencing (MPSS) on microbead arrays
    Brenner, S
    Johnson, M
    Bridgham, J
    Golda, G
    Lloyd, DH
    Johnson, D
    Luo, SJ
    McCurdy, S
    Foy, M
    Ewan, M
    Roth, R
    George, D
    Eletr, S
    Albrecht, G
    Vermaas, E
    Williams, SR
    Moon, K
    Burcham, T
    Pallas, M
    DuBridge, RB
    Kirchner, J
    Fearon, K
    Mao, J
    Corcoran, K
    [J]. NATURE BIOTECHNOLOGY, 2000, 18 (06) : 630 - 634
  • [3] BROVKO LY, 1994, BIOCHEMISTRY-MOSCOW+, V59, P195
  • [4] Sensitive and quantitative universal Pyrosequencing™ methylation analysis of CpG sites
    Colella, S
    Shen, L
    Baggerly, KA
    Issa, JPJ
    Krahe, R
    [J]. BIOTECHNIQUES, 2003, 35 (01) : 146 - +
  • [5] KINETIC MECHANISM OF DNA-POLYMERASE-I (KLENOW FRAGMENT) - IDENTIFICATION OF A 2ND CONFORMATIONAL CHANGE AND EVALUATION OF THE INTERNAL EQUILIBRIUM-CONSTANT
    DAHLBERG, ME
    BENKOVIC, SJ
    [J]. BIOCHEMISTRY, 1991, 30 (20) : 4835 - 4843
  • [6] ATP SULFURYLASE-DEPENDENT ASSAYS FOR INORGANIC PYROPHOSPHATE - APPLICATIONS TO DETERMINING THE EQUILIBRIUM-CONSTANT AND REVERSE DIRECTION KINETICS OF THE PYROPHOSPHATASE REACTION, MAGNESIUM BINDING TO ORTHO-PHOSPHATE, AND UNKNOWN CONCENTRATIONS OF PYROPHOSPHATE
    DALEY, LA
    RENOSTO, F
    SEGEL, IH
    [J]. ANALYTICAL BIOCHEMISTRY, 1986, 157 (02) : 385 - 395
  • [7] DEAMER DW, 2002, ELECTROPHORESIS, V23, P2583
  • [8] DRMANAC R, 1989, GENOMICS, V4, P114
  • [9] Pyrosequencing™:: An accurate detection platform for single nucleotide polymorphisms
    Fakhrai-Rad, H
    Pourmand, N
    Ronaghi, M
    [J]. HUMAN MUTATION, 2002, 19 (05) : 479 - 485
  • [10] Mutation detection by pyrosequencing:: sequencing of exons 5-8 of the p53 tumor suppressor gene
    Garcia, CA
    Ahmadian, A
    Gharizadeh, B
    Lundeberg, J
    Ronaghi, M
    Nyrén, P
    [J]. GENE, 2000, 253 (02) : 249 - 257