TY - JOUR
T1 - DNA-enrichment microfluidic chip for chromatin immunoprecipitation
AU - Oh, Hyun Jik
AU - Park, Joong Yull
AU - Park, Sung Eun
AU - Lee, Bo Yun
AU - Park, Jong Sung
AU - Kim, Suel Kee
AU - Yoon, Tae Joong
AU - Lee, Sang Hoon
PY - 2009/4/15
Y1 - 2009/4/15
N2 - Chromatin immunoprecipitation (ChIP) is a powerful and widely applied technique for detecting association of individual proteins with specific genomic regions; the technique requires several complex steps and is tedious. In this paper, we develop a microbead-packed microfluidic chip which eliminates most of the laborious, timeconsuming, and skill-dependent processes of the ChIP procedure. A computational fluid dynamics model was established to analyze fluidic behavior in a microbeadpacked microchannel. With the use of the new chip, a ChIP procedure was performed to purify the GAPDH (glyceraldehyde 3-phosphate dehydrogenase) gene from human embryonic kidney cells (cell line 293). The ChIP capability of the microfluidic chip was evaluated and compared with that of a commercial assay kit; the precipitation performance of both methods was almost identical as shown by quantitative measurement of DNA. However, our chip offers the advantage of low resin volume, and the experimental time is greatly reduced. In addition, our method is less dependent on individual technical skill. Therefore, we expect that our microfluidic chip-based ChIP method will be widely used in DNA-, gene-, and protein-related research and will improve experimental efficiency.
AB - Chromatin immunoprecipitation (ChIP) is a powerful and widely applied technique for detecting association of individual proteins with specific genomic regions; the technique requires several complex steps and is tedious. In this paper, we develop a microbead-packed microfluidic chip which eliminates most of the laborious, timeconsuming, and skill-dependent processes of the ChIP procedure. A computational fluid dynamics model was established to analyze fluidic behavior in a microbeadpacked microchannel. With the use of the new chip, a ChIP procedure was performed to purify the GAPDH (glyceraldehyde 3-phosphate dehydrogenase) gene from human embryonic kidney cells (cell line 293). The ChIP capability of the microfluidic chip was evaluated and compared with that of a commercial assay kit; the precipitation performance of both methods was almost identical as shown by quantitative measurement of DNA. However, our chip offers the advantage of low resin volume, and the experimental time is greatly reduced. In addition, our method is less dependent on individual technical skill. Therefore, we expect that our microfluidic chip-based ChIP method will be widely used in DNA-, gene-, and protein-related research and will improve experimental efficiency.
UR - http://www.scopus.com/inward/record.url?scp=65249161137&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=65249161137&partnerID=8YFLogxK
U2 - 10.1021/ac802034s
DO - 10.1021/ac802034s
M3 - Article
C2 - 19298056
AN - SCOPUS:65249161137
SN - 0003-2700
VL - 81
SP - 2832
EP - 2839
JO - Analytical Chemistry
JF - Analytical Chemistry
IS - 8
ER -