Experimental investigation of confinement effect in single molecule amplification via real-time digital PCR on a multivolume droplet array SlipChip

被引:2
|
作者
Luo, Yang [1 ]
Hu, Qixin [1 ]
Yu, Yan [1 ]
Lyu, Weiyuan [1 ]
Shen, Feng [1 ]
机构
[1] Shanghai Jiao Tong Univ, Sch Biomed Engn, 1954 Hua Shan Rd, Shanghai 200030, Peoples R China
基金
中国国家自然科学基金; 上海市自然科学基金;
关键词
Digital PCR; Confinement; Microfluidics; SlipChip; Real-time; POLYMERASE-CHAIN-REACTION; ISOTHERMAL AMPLIFICATION; QUANTIFICATION; CHIP; DNA; ASSAY;
D O I
10.1016/j.aca.2024.342541
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Background: Digital polymerase chain reaction (digital PCR) is an important quantitative nucleic acid analysis method in both life science research and clinical diagnostics. One important hypothesis is that by physically constraining a single nucleic acid molecule in a small volume, the relative concentration can be increased therefore further improving the analysis performance, and this is commonly defined as the confinement effect in digital PCR. However, experimental investigation of this confinement effect can be challenging since it requires a microfluidic device that can generate partitions of different volumes and an instrument that can monitor the kinetics of amplification. (96). Results: Here, we developed a real-time digital PCR system with a multivolume droplet array SlipChip (MudaSlipChip) that can generate droplet of 125 nL, 25 nL, 5 nL, and 1 nL by a simple "load -slip" operation. In the digital region, by reducing the volume, the relative concentration is increased, the amplification kinetic can be accelerated, and the time to reach the fluorescence threshold, or Cq value, can be reduced. When the copy number per well is much higher than one, the relative concentration is independent of the partition volume, thus the amplification kinetics are similar in different volume partitions. This system is not limited to studying the kinetics of digital nucleic acid amplification, it can also extend the dynamic range of the digital nucleic acid analysis by additional three orders of magnitude by combining a digital and an analog quantification algorithm. (140). Significance: In this study, we experimentally investigated for the first time the confinement effect in the community of digital PCR via a new real-time digital PCR system with a multivolume droplet array SlipChip (MudaSlipChip). And a wider dynamic range of quantification methods compared to conventional digital PCR was validated by this system. This system provides emerging opportunities for life science research and clinical diagnostics. (63).
引用
收藏
页数:8
相关论文
共 50 条
  • [31] Performance of a real-time PCR-based approach and droplet digital PCR in detecting human parechovirus type 3 RNA
    Aizawa, Yuta
    Koyama, Akihide
    Ishihara, Tomohiko
    Onodera, Osamu
    Saitoh, Akihiko
    JOURNAL OF CLINICAL VIROLOGY, 2016, 84 : 27 - 31
  • [32] Optimised multiplex droplet digital PCR is more precise, but not more sensitive, than real-time PCR for the detection of allergenic peanut
    Eischeid, Anne C.
    FOOD ADDITIVES AND CONTAMINANTS PART A-CHEMISTRY ANALYSIS CONTROL EXPOSURE & RISK ASSESSMENT, 2022, 39 (11): : 1797 - 1805
  • [33] Increased Robustness of Single-Molecule Counting with Microfluidics, Digital Isothermal Amplification, and a Mobile Phone versus Real-Time Kinetic Measurements
    Selck, David A.
    Karymov, Mikhail A.
    Sun, Bing
    Ismagilov, Rustem F.
    ANALYTICAL CHEMISTRY, 2013, 85 (22) : 11129 - 11136
  • [34] Investigation of meat species adulteration in beef-based meat products via real-time PCR in Turkiye
    Ozlu, Hayrunnisa
    Cevik, Burak
    Atasever, Mustafa
    Sarialioglu, Muhammet Furkan
    Polat, Betul Alkan
    QUALITY ASSURANCE AND SAFETY OF CROPS & FOODS, 2023, 15 (04) : 42 - 48
  • [35] Comparison of Real-Time Quantitative PCR and Digital Droplet PCR for BCR-ABL1 Monitoring in Patients with Chronic Myeloid Leukemia
    Franke, Georg-Nikolaus
    Maier, Jacqueline
    Wildenberger, Kathrin
    Cross, Michael
    Giles, Francis J.
    Mueller, Martin C.
    Hochhaus, Andreas
    Niederwieser, Dietger
    Lange, Thoralf
    JOURNAL OF MOLECULAR DIAGNOSTICS, 2020, 22 (01): : 81 - 89
  • [36] Droplet Digital Polymerase Chain Reaction (PCR) Outperforms Real-Time PCR in the Detection of Environmental DNA from an Invasive Fish Species
    Doi, Hideyuki
    Takahara, Teruhiko
    Minamoto, Toshifumi
    Matsuhashi, Saeko
    Uchii, Kimiko
    Yamanaka, Hiroki
    ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2015, 49 (09) : 5601 - 5608
  • [37] Effect of Source of DNA on the Quantitative Analysis of Genetically Engineered Traits Using Digital PCR and Real-Time PCR
    Demeke, Tigst
    Malabanan, Jemima
    Holigroski, Michelle
    Eng, Monika
    JOURNAL OF AOAC INTERNATIONAL, 2017, 100 (02) : 492 - 498
  • [38] Quantitative real-time polymerase chain reaction (PCR) and droplet digital PCR duplex assays for detecting Zostera marina DNA in coastal sediments
    Hamaguchi, Masami
    Shimabukuro, Hiromori
    Hori, Masakazu
    Yoshida, Goro
    Terada, Tomoko
    Miyajima, Toshihiro
    LIMNOLOGY AND OCEANOGRAPHY-METHODS, 2018, 16 (04): : 253 - 264
  • [39] Quantification of BK Virus Standards by Quantitative Real-Time PCR and Droplet Digital PCR Is Confounded by Multiple Virus Populations in the WHO BKV International Standard
    Bateman, Allen C.
    Greninger, Alexander L.
    Atienza, Ederlyn E.
    Limaye, Ajit P.
    Jerome, Keith R.
    Cook, Linda
    CLINICAL CHEMISTRY, 2017, 63 (03) : 761 - 769
  • [40] Committed change of real-time quantitative PCR to droplet digital PCR for monitoring BCR::ABL1 transcripts in tyrosine kinase inhibitor treated CML
    Kongruang, Adcharee
    Limsuwanachot, Nittaya
    Magmuang, Sutada
    Areesirisuk, Prapatsorn
    Niparuck, Pimjai
    Siriboonpiputtana, Teerapong
    Rerkamnuaychoke, Budsaba
    HEMATOLOGY, 2023, 28 (01)