한빛사논문
Kyung Ho Kima,1, Seon Joo Parka,1, Chul Soon Parka, Sung Eun Seoa, Jiyeon Leea, Jinyeong Kima, Seung Hwan Leeb, Soohyun Leea, Jun-Seob Kima, Choong-Min Ryua, Dongeun Yongc, Hyeonseok Yoond, Hyun Seok Songe, Sang Hun Leef,*, Oh Seok Kwona,g,*
aInfectious Disease Research Center, Korea Research Institute of Bioscience and Biotechnology (KRIBB), Daejeon, 34141, Republic of Korea
bDepartment of Bionano Engineering, Hanyang University, Ansan, Republic of Korea
cDepartment of Laboratory Medicine and Research Institute of Bacterial Resistance, Yonsei University College of Medicine, Seoul, Republic of Korea
dSchool of Polymer Science and Engineering and Department of Polymer Engineering, Graduate School, Chonnam National University, Gwangju, 61186, Republic of Korea
eSensor System Research Center, Korea Institute of Science and Technology, Seoul, 02792, Republic of Korea
fDepartment of Bioengineering, University of California Berkeley, CA, 94720, USA
gDepartment of Nanobiotechnology, Korea University of Science and Technology (UST), Republic of Korea
1These authors contributed equally to this work.
*Corresponding author
Abstract
Current techniques for Gram-typing and for diagnosing a pathogen at the early infection stage rely on Gram stains, cultures, Enzyme linked immunosorbent assay (ELISA), polymerase chain reaction (PCR), and gene microarrays, which are labor-intensive and time-consuming approaches. In addition, a delayed or imprecise diagnosis of clinical pathogenic bacteria leads to a life-threatening emergency or overuse of antibiotics and a high-rate occurrence of antimicrobial-resistance microbes. Herein, we report high-performance antibiotics (as bioprobes) conjugated graphene micropattern field-effect transistors (ABX-GMFETs) to facilitate on-site Gram-typing and help in the detection of the presence or absence of Gram-negative and -positive bacteria in the samples. The ABX-GMFET platform, which consists of recognition probes and GM transistors conjugated with novel interfacing chemical compounds, was integrated into the microfluidics to minimize the required human intervention and facilitate automation. The mechanism of binding of ABX-GMFET was based on a charge or chemical moiety interaction between the bioprobes and target bacteria. Subsequently, ABX-GMFETs exhibited unprecedented high sensitivity with a limit of detection (LOD) of 100 CFU/mL (1–9 CFU/mL), real-time target specificity.
Keywords : Portable biosensor; Graphene field-effect transistor; Interfacing chemistry; Microfluidics; Real-time monitoring; Bioprobes
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