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

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 imprinti...

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Bibliographic Details
Main Authors: Bartold, K. (Author), Borowicz, P. (Author), Iskierko, Z. (Author), Kalecki, J. (Author), Kutner, W. (Author), Lin, C.-Y (Author), Lin, H.-Y (Author), Noworyta, K. (Author), Sharma, P.S (Author)
Format: Article
Language:English
Published: Elsevier Ltd 2022
Subjects:
IPF
MIP
Online Access:View Fulltext in Publisher
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001 0.1016-j.bios.2022.114203
008 220421s2022 CNT 000 0 und d
020 |a 09565663 (ISSN) 
245 1 0 |a Molecularly imprinted polymer-based extended-gate field-effect transistor (EG-FET) chemosensor for selective determination of matrix metalloproteinase-1 (MMP-1) protein 
260 0 |b Elsevier Ltd  |c 2022 
856 |z View Fulltext in Publisher  |u https://doi.org/10.1016/j.bios.2022.114203 
520 3 |a 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. © 2022 The Authors 
650 0 4 |a BLAST 
650 0 4 |a BLAST 
650 0 4 |a Chemosensor 
650 0 4 |a Chemosensor 
650 0 4 |a Chemo-sensors 
650 0 4 |a EG-FET 
650 0 4 |a Electropolymerization 
650 0 4 |a Epitope imprinting 
650 0 4 |a Epitope imprinting 
650 0 4 |a Epitopes 
650 0 4 |a Extended-gate field-effect transistor 
650 0 4 |a Extended-gate field-effect transistors 
650 0 4 |a Field effect transistors 
650 0 4 |a Idiopathic pulmonary fibrosis 
650 0 4 |a Idiopathic pulmonary fibrosis 
650 0 4 |a IPF 
650 0 4 |a Matrix metalloproteinase-1 
650 0 4 |a Matrix metalloproteinase-1 protein 
650 0 4 |a MIP 
650 0 4 |a MMP-1 protein 
650 0 4 |a Molecularly imprinted polymer 
650 0 4 |a Molecularly Imprinted Polymer 
650 0 4 |a Proteins 
650 0 4 |a Thin film circuits 
650 0 4 |a Thin films 
700 1 0 |a Bartold, K.  |e author 
700 1 0 |a Borowicz, P.  |e author 
700 1 0 |a Iskierko, Z.  |e author 
700 1 0 |a Kalecki, J.  |e author 
700 1 0 |a Kutner, W.  |e author 
700 1 0 |a Lin, C.-Y.  |e author 
700 1 0 |a Lin, H.-Y.  |e author 
700 1 0 |a Noworyta, K.  |e author 
700 1 0 |a Sharma, P.S.  |e author 
773 |t Biosensors and Bioelectronics