Molecularly imprinted polymer-based extended-gate field-effect transistor (EG-FET) chemosensor for selective determination of matrix metalloproteinase-1 (MMP-1) protein

被引:29
作者
Bartold, Katarzyna [1 ]
Iskierko, Zofia [1 ]
Borowicz, Pawel [1 ]
Noworyta, Krzysztof [1 ]
Lin, Chu-Yun [2 ]
Kalecki, Jakub [1 ]
Sharma, Piyush Sindhu [1 ]
Lin, Hung-Yin [2 ]
Kutner, Wlodzimierz [1 ,3 ]
机构
[1] Polish Acad Sci, Inst Phys Chem, Kasprzaka 44-52, PL-01224 Warsaw, Poland
[2] Natl Univ Kaohsiung, Dept Chem & Mat Engn, Kaohsiung 81148, Taiwan
[3] Cardinal Stefan Wyszynski Univ Warsaw, Fac Math & Nat Sci, Sch Sci, Woycickiego 1-3, PL-01938 Warsaw, Poland
关键词
Epitope imprinting; Molecularly imprinted polymer; MIP; MMP-1; protein; Idiopathic pulmonary fibrosis; IPF; BLAST; Extended-gate field-effect transistor; EG-FET; Chemosensor; PULMONARY-FIBROSIS; TRIPHENYLAMINE; PATHOGENESIS; RECOGNITION; BIOMARKERS;
D O I
10.1016/j.bios.2022.114203
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
A conducting molecularly imprinted polymer (MIP) film was integrated with an extended-gate field-effect transistor (EG-FET) transducer to determine epitopes of matrix metalloproteinase-1 (MMP-1) protein biomarker of idiopathic pulmonary fibrosis (IPF) selectively. Most suitable epitopes for imprinting were selected with Basic Local Alignment Search Tool software. From a pool of MMP-1 epitopes, the two, i.e., MIAHDFPGIGHK and HGYPKDIYSS, the relatively short ones, most promising for MMP-1 determination, were selected, mainly considering their advantageous outermost location in the protein molecule and stability against aggregation. MIPs templated with selected epitopes of the MMP-1 protein were successfully prepared by potentiodynamic electropolymerization and simultaneously deposited as thin films on electrodes. The chemosensors, constructed of MIP films integrated with EG-FET, proved useful in determining these epitopes even in a medium as complex as a control serum. The limit of detection for the MIAHDFPGIGHK and HGYPKDIYSS epitope was ~60 and 20 nM, respectively. Moreover, the chemosensors selectively recognized whole MMP-1 protein in the 50-500 nM concentration range in buffered control serum samples.
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页数:9
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