Sanchez J Aquiles, Pierce Kenneth E, Rice John E, Wangh Lawrence J
Department of Biology, MS 008, Brandeis University, 415 South Street, Waltham, MA 02454-9110, USA.
Proc Natl Acad Sci U S A. 2004 Feb 17;101(7):1933-8. doi: 10.1073/pnas.0305476101. Epub 2004 Feb 9.
Conventional asymmetric PCR is inefficient and difficult to optimize because limiting the concentration of one primer lowers its melting temperature below the reaction annealing temperature. Linear-After-The-Exponential (LATE)-PCR describes a new paradigm for primer design that renders assays as efficient as symmetric PCR assays, regardless of primer ratio. LATE-PCR generates single-stranded products with predictable kinetics for many cycles beyond the exponential phase. LATE-PCR also introduces new probe design criteria that uncouple hybridization probe detection from primer annealing and extension, increase probe reliability, improve allele discrimination, and increase signal strength by 80-250% relative to symmetric PCR. These improvements in PCR are particularly useful for real-time quantitative analysis of target numbers in small samples. LATE-PCR is adaptable to high throughput applications in fields such as clinical diagnostics, biodefense, forensics, and DNA sequencing. We showcase LATE-PCR via amplification of the cystic fibrosis CFDelta508 allele and the Tay-Sachs disease TSD 1278 allele from single heterozygous cells.
传统的不对称PCR效率低下且难以优化,因为限制一种引物的浓度会使其解链温度降至反应退火温度以下。指数后线性(LATE)-PCR描述了一种新的引物设计范式,无论引物比例如何,该方法都能使检测效率与对称PCR检测一样高。LATE-PCR在指数期后的多个循环中产生具有可预测动力学的单链产物。LATE-PCR还引入了新的探针设计标准,使杂交探针检测与引物退火和延伸解耦,提高了探针的可靠性,改善了等位基因区分,并使信号强度相对于对称PCR提高了80%-250%。PCR的这些改进对于小样本中靶标数量的实时定量分析特别有用。LATE-PCR适用于临床诊断、生物防御、法医学和DNA测序等领域的高通量应用。我们通过从单个杂合细胞中扩增囊性纤维化CFDelta508等位基因和泰-萨克斯病TSD 1278等位基因来展示LATE-PCR。