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Immuno-Sensing at Ultra-Low Concentration of TG2 Protein by Organic Electrochemical Transistors
Transglutaminase 2 (TG2) is a ubiquitously expressed member of the transglutaminase family with Ca2+-dependent protein crosslinking activity. Its subcellular localization is crucial in determining its function, and indeed, TG2 is found in the extracellular matrix, mitochondria, recycling endosomes,...
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Published in: | Biosensors (Basel) 2023-03, Vol.13 (4), p.448 |
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description | Transglutaminase 2 (TG2) is a ubiquitously expressed member of the transglutaminase family with Ca2+-dependent protein crosslinking activity. Its subcellular localization is crucial in determining its function, and indeed, TG2 is found in the extracellular matrix, mitochondria, recycling endosomes, plasma membrane, cytosol, and nucleus because it is associated with cell growth, differentiation, and apoptosis. It is involved in several pathologies, such as celiac disease, cardiovascular, hepatic, renal, and fibrosis diseases, carrying out opposite functions of up and down regulation in the progression of the same pathology. Therefore, this fine regulation requires a very sensitive and specific method of identification of TG2, which is to be detected in very small quantities in a deregulated condition. Here, we demonstrate the possibility of detecting TG2 down to attomolar concentration by using organic electrochemical transistors driven by gold electrodes functionalized with anti-TG2 antibodies. In particular, a direct correlation between the TG2 concentration and the transistor transconductance values, as extracted from typical transfer curves, was found. Overall, our findings highlight the potentialities of this new biosensing approach for the detection of TG2 in the context of pathological diseases, offering a rapid and cost-effective alternative to traditional methods. |
doi_str_mv | 10.3390/bios13040448 |
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Its subcellular localization is crucial in determining its function, and indeed, TG2 is found in the extracellular matrix, mitochondria, recycling endosomes, plasma membrane, cytosol, and nucleus because it is associated with cell growth, differentiation, and apoptosis. It is involved in several pathologies, such as celiac disease, cardiovascular, hepatic, renal, and fibrosis diseases, carrying out opposite functions of up and down regulation in the progression of the same pathology. Therefore, this fine regulation requires a very sensitive and specific method of identification of TG2, which is to be detected in very small quantities in a deregulated condition. Here, we demonstrate the possibility of detecting TG2 down to attomolar concentration by using organic electrochemical transistors driven by gold electrodes functionalized with anti-TG2 antibodies. In particular, a direct correlation between the TG2 concentration and the transistor transconductance values, as extracted from typical transfer curves, was found. Overall, our findings highlight the potentialities of this new biosensing approach for the detection of TG2 in the context of pathological diseases, offering a rapid and cost-effective alternative to traditional methods.</description><identifier>ISSN: 2079-6374</identifier><identifier>EISSN: 2079-6374</identifier><identifier>DOI: 10.3390/bios13040448</identifier><identifier>PMID: 37185523</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>Analysis ; Antibodies ; Antigens ; Apoptosis ; Autoimmune diseases ; Biosensors ; Calcium ; Calcium ions ; Celiac disease ; Cell differentiation ; Chemical properties ; Crosslinking ; Cytosol ; Deregulation ; diagnostic devices ; Disease ; Electric properties ; Electrochemical analysis ; Electrochemistry ; Electrodes ; Endosomes ; Equipment and supplies ; Ethanol ; Extracellular matrix ; Fibrosis ; functionalization ; GTP-Binding Proteins - metabolism ; Identification methods ; Immunosensors ; Liver ; Liver diseases ; Localization ; Methods ; Mitochondria ; organic electrochemical transistors ; Plasma etching ; Protein Glutamine gamma Glutamyltransferase 2 ; Protein turnover ; Proteins ; Semiconductor devices ; specificity ; TG2 protein ; Transconductance ; Transglutaminase 2 ; Transglutaminases ; Transglutaminases - metabolism ; Transistors</subject><ispartof>Biosensors (Basel), 2023-03, Vol.13 (4), p.448</ispartof><rights>COPYRIGHT 2023 MDPI AG</rights><rights>2023 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). 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Its subcellular localization is crucial in determining its function, and indeed, TG2 is found in the extracellular matrix, mitochondria, recycling endosomes, plasma membrane, cytosol, and nucleus because it is associated with cell growth, differentiation, and apoptosis. It is involved in several pathologies, such as celiac disease, cardiovascular, hepatic, renal, and fibrosis diseases, carrying out opposite functions of up and down regulation in the progression of the same pathology. Therefore, this fine regulation requires a very sensitive and specific method of identification of TG2, which is to be detected in very small quantities in a deregulated condition. Here, we demonstrate the possibility of detecting TG2 down to attomolar concentration by using organic electrochemical transistors driven by gold electrodes functionalized with anti-TG2 antibodies. In particular, a direct correlation between the TG2 concentration and the transistor transconductance values, as extracted from typical transfer curves, was found. Overall, our findings highlight the potentialities of this new biosensing approach for the detection of TG2 in the context of pathological diseases, offering a rapid and cost-effective alternative to traditional methods.</description><subject>Analysis</subject><subject>Antibodies</subject><subject>Antigens</subject><subject>Apoptosis</subject><subject>Autoimmune diseases</subject><subject>Biosensors</subject><subject>Calcium</subject><subject>Calcium ions</subject><subject>Celiac disease</subject><subject>Cell differentiation</subject><subject>Chemical properties</subject><subject>Crosslinking</subject><subject>Cytosol</subject><subject>Deregulation</subject><subject>diagnostic devices</subject><subject>Disease</subject><subject>Electric properties</subject><subject>Electrochemical analysis</subject><subject>Electrochemistry</subject><subject>Electrodes</subject><subject>Endosomes</subject><subject>Equipment and supplies</subject><subject>Ethanol</subject><subject>Extracellular matrix</subject><subject>Fibrosis</subject><subject>functionalization</subject><subject>GTP-Binding Proteins - 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Its subcellular localization is crucial in determining its function, and indeed, TG2 is found in the extracellular matrix, mitochondria, recycling endosomes, plasma membrane, cytosol, and nucleus because it is associated with cell growth, differentiation, and apoptosis. It is involved in several pathologies, such as celiac disease, cardiovascular, hepatic, renal, and fibrosis diseases, carrying out opposite functions of up and down regulation in the progression of the same pathology. Therefore, this fine regulation requires a very sensitive and specific method of identification of TG2, which is to be detected in very small quantities in a deregulated condition. Here, we demonstrate the possibility of detecting TG2 down to attomolar concentration by using organic electrochemical transistors driven by gold electrodes functionalized with anti-TG2 antibodies. In particular, a direct correlation between the TG2 concentration and the transistor transconductance values, as extracted from typical transfer curves, was found. Overall, our findings highlight the potentialities of this new biosensing approach for the detection of TG2 in the context of pathological diseases, offering a rapid and cost-effective alternative to traditional methods.</abstract><cop>Switzerland</cop><pub>MDPI AG</pub><pmid>37185523</pmid><doi>10.3390/bios13040448</doi><orcidid>https://orcid.org/0000-0002-1990-0119</orcidid><orcidid>https://orcid.org/0000-0002-3506-216X</orcidid><orcidid>https://orcid.org/0000-0003-4858-4853</orcidid><orcidid>https://orcid.org/0000-0003-4570-2674</orcidid><orcidid>https://orcid.org/0000-0002-9247-6852</orcidid><orcidid>https://orcid.org/0000-0002-5866-223X</orcidid><orcidid>https://orcid.org/0000-0002-8852-5703</orcidid><orcidid>https://orcid.org/0000-0002-4500-4457</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Analysis Antibodies Antigens Apoptosis Autoimmune diseases Biosensors Calcium Calcium ions Celiac disease Cell differentiation Chemical properties Crosslinking Cytosol Deregulation diagnostic devices Disease Electric properties Electrochemical analysis Electrochemistry Electrodes Endosomes Equipment and supplies Ethanol Extracellular matrix Fibrosis functionalization GTP-Binding Proteins - metabolism Identification methods Immunosensors Liver Liver diseases Localization Methods Mitochondria organic electrochemical transistors Plasma etching Protein Glutamine gamma Glutamyltransferase 2 Protein turnover Proteins Semiconductor devices specificity TG2 protein Transconductance Transglutaminase 2 Transglutaminases Transglutaminases - metabolism Transistors |
title | Immuno-Sensing at Ultra-Low Concentration of TG2 Protein by Organic Electrochemical Transistors |
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