发明名称 RAPID, HIGHLY-SENSITIVE, AND HIGHLY-SPECIFIC NUCLEIC ACID DETECTION
摘要 A nucleic acid (NA) detection method combines ultra-specific probe, on-chip isotachophoresis (ITP) which can separate single strand and double strand NAs, and enzyme amplification. The ITP device has a sieving matrix between the LE (leading electrolyte) and TE (trailing electrolyte) reservoirs, for separating double-strand and single-strand NAs. The LE or TE reservoir also contains a spacer ion having a mobility between the LE and the TE. The sample and a double-strand NA probe is added to the TE reservoir, the probe being formed of a protector strand modified with a fluorescent molecule and a complement strand, where the protector strand is released in the presence of the target NA. Fluorescent signal is detected downstream of the sieving matrix. Alternatively, the protector strand is modified with an enzyme and a single-strand NA modified with a substrate of the enzyme is added to the reaction mixture downstream of the sieving matrix.
申请公布号 US2016299100(A1) 申请公布日期 2016.10.13
申请号 US201615063355 申请日期 2016.03.07
申请人 KONICA MINOLTA LABORATORY U.S.A., INC. 发明人 Yamamoto Noriaki
分类号 G01N27/447;B01L3/00;C12Q1/68 主分类号 G01N27/447
代理机构 代理人
主权项 1. A method for detecting a target nucleic acid, comprising: providing an on-chip isotachophoresis (ITP) device, which has a first reservoir containing a leading electrolyte (LE), a second reservoir containing a trailing electrolyte (TE), and a microfluidic channel connecting the first and second reservoirs, wherein a region of the microfluidic channel is provided with a sieving matrix for separating double-strand and single-strand nucleic acids, wherein the first or second reservoirs further containing a spacer ion having a mobility between that of the LE and the TE; providing a probe which is a double-strand nucleic acid formed of a protector strand nucleic acid modified with a fluorescent molecule and a complement strand nucleic acid, wherein the protector strand nucleic acid is released in the presence of the target nucleic acid; adding the probe and a sample to the first reservoir; applying a voltage between the first and second reservoirs; and detecting a fluorescent signal in the microfluidic channel at an interface between the LE and the spacer ion.
地址 San Mateo CA US