High-throughput class IHLA genotyping using fluorescence resonance energy transfer (FRET) probes and sequence-specific primer-polymerase chain reaction (SSP-PCR)

被引:8
作者
Gelsthorpe, AR [1 ]
Wells, RS [1 ]
Lowe, AP [1 ]
Tonks, S [1 ]
Bodmer, JG [1 ]
Bodmer, WF [1 ]
机构
[1] John Radcliffe Hosp, Canc & Immunogenet Lab, Imperial Canc Res Fund, Inst Mol Med, Oxford OX3 9DS, England
来源
TISSUE ANTIGENS | 1999年 / 54卷 / 06期
关键词
HLA; genotyping; SSP-PCR; FRET; automation;
D O I
10.1034/j.1399-0039.1999.540611.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
We have developed a semi-automated HLA class I typing system utilising TET/TAMRA-labelled fluorescence resonance energy transfer (FRET) hydrolysis probes. The results from 87 individuals are in full concordance with serology and conventional gel-based systems. This assay replaces labour-intensive conventional gel-based DNA typing and has a higher allelic resolution than serology. Our approach differs from previously published fluorogenic probe typing protocols in that it provides simultaneous typing of HLA-A, -B and -C loci to medium resolution. Furthermore, by using equipment that is not specific to FRET probe analysis our system has in-built expansion capacity to 384 reactions per plate, thus making it applicable to high-throughput population screening. Automation is achieved through the use of computer software which analyses direct input from the fluorescence reader, allowing high throughput with a low inherent error rate.
引用
收藏
页码:603 / 614
页数:12
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