Shi Chanjuan, Eshleman Susan H, Jones Dana, Fukushima Noriyoshi, Hua Li, Parker Antony R, Yeo Charles J, Hruban Ralph H, Goggins Michael G, Eshleman James R
Department of Pathology, Johns Hopkins University School of Medicine, 720 Rutland Avenue, Baltimore, Maryland 21205, USA.
Nat Methods. 2004 Nov;1(2):141-7. doi: 10.1038/nmeth713. Epub 2004 Oct 21.
We developed the LigAmp assay for sensitive detection and accurate quantification of viruses and cells with single-base mutations. In LigAmp, two oligonucleotides are hybridized adjacently to a DNA template. One oligonucleotide matches the target sequence and contains a probe sequence. If the target sequence is present, the oligonucleotides are ligated together and detected using real-time PCR. LigAmp detected KRAS2 mutant DNA at 0.01% in mixtures of different cell lines. KRAS2 mutations were also detected in pancreatic duct juice from patients with pancreatic cancer. LigAmp detected the K103N HIV-1 drug resistance mutation at 0.01% in plasmid mixtures and at approximately 0.1% in DNA amplified from plasma HIV-1. Detection in both systems is linear over a broad dynamic range. Preliminary evidence indicates that reactions can be multiplexed. This assay may find applications in the diagnosis of genetic disorders and the management of patients with cancer and infectious diseases.
我们开发了LigAmp检测法,用于灵敏检测和准确定量具有单碱基突变的病毒和细胞。在LigAmp检测法中,两条寡核苷酸与DNA模板相邻杂交。一条寡核苷酸与靶序列匹配并包含一个探针序列。如果存在靶序列,寡核苷酸会连接在一起,并使用实时PCR进行检测。LigAmp在不同细胞系的混合物中能检测到0.01%的KRAS2突变DNA。在胰腺癌患者的胰管液中也检测到了KRAS2突变。LigAmp在质粒混合物中能检测到0.01%的K103N HIV-1耐药突变,在从血浆HIV-1扩增的DNA中能检测到约0.1%的该突变。在两个系统中的检测在很宽的动态范围内呈线性。初步证据表明反应可以进行多重检测。该检测法可能在遗传疾病诊断以及癌症和传染病患者的管理中找到应用。