A fully integrated microchip system for automated forensic short tandem repeat analysis

被引:18
|
作者
Han, Junping [1 ,2 ,3 ]
Gan, Wupeng [1 ]
Zhuang, Bin [1 ]
Sun, Jing [2 ]
Zhao, Lei [2 ]
Ye, Jian [2 ]
Liu, Yao [2 ]
Li, Cai-Xia [2 ]
Liu, Peng [1 ]
机构
[1] Tsinghua Univ, Dept Biomed Engn, Sch Med, Collaborat Innovat Ctr Diag & Treatment Infect Di, Beijing 100084, Peoples R China
[2] Inst Forens Sci, Key Lab Forens Genet, Beijing Engn Res Ctr Crime Scene Evidence Examina, Natl Engn Lab Crime Scene Evidence Examinat, Beijing 100038, Peoples R China
[3] Beijing Publ Secur Bur, Technol Dept Chaoyang Subbur, Beijing 100102, Peoples R China
关键词
MULTIPLEX PCR AMPLIFICATION; DNA ANALYSIS; HUMAN IDENTIFICATION; STR ANALYSIS; MICROFLUIDIC DEVICES; REFERENCE SAMPLES; RAPIDHIT(TM) 200; ELECTROPHORESIS; CAPILLARY; MICRODEVICE;
D O I
10.1039/c7an00295e
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
We have successfully developed an integrated microsystem that combines two plastic microchips for DNA extraction and PCR amplification with a glass capillary array electrophoresis chip together in a compact control and detection instrument for automated forensic short tandem repeat (STR) analysis. DNA extraction followed by an "in situ PCR" was conducted in a single reaction chamber of the microchip based on a filter paper-based extraction methodology. PCR products were then mixed with sizing standards by an injection electrode and injected into the electrophoresis chip for four-color confocal fluorescence detection. The entire STR analysis can be completed in about two hours without any human intervention. Since the 15-plex STR system has a more stringent requirement for PCR efficiency, we optimized the structure of the plastic DNA extraction and amplification chip, in which the reaction chamber was formed by sandwiching a hollow structure layer with two blank cover layers, to reduce the adsorption of PCR reagents to the surfaces. In addition, PCR additives, bovine serum albumin, poly(ethylene glycol), and more magnesium chloride were included into the on-chip multiplex STR system. The limit-of-detection study demonstrated that our microsystem was able to produce full 15-plex STR profiles from 3.75 ng standard K562 DNA. Buccal swab and whole blood samples were also successfully typed by our system, validating the feasibility of performing rapid DNA typing in a "sample-in-answer-out" manner for on-site forensic human identification.
引用
收藏
页码:2004 / 2012
页数:9
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