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Microfluidic Protein Imaging Platform: Study of Tau Protein Aggregation and Alzheimer’s Drug Response

Tau protein aggregation is identified as one of the key phenomena associated with the onset and progression of Alzheimer’s disease. In the present study, we performed on-chip confocal imaging of tau protein aggregation and tau–drug interactions using a spiral-shaped passive micromixing platform. Num...

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Autores principales: Jain, Shubha, Swain, Sarpras, Das, Lopamudra, Swain, Sarita, Giri, Lopamudra, Kondapi, Anand Kumar, Narayanan Unni, Harikrishnan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7763324/
https://www.ncbi.nlm.nih.gov/pubmed/33322166
http://dx.doi.org/10.3390/bioengineering7040162
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author Jain, Shubha
Swain, Sarpras
Das, Lopamudra
Swain, Sarita
Giri, Lopamudra
Kondapi, Anand Kumar
Narayanan Unni, Harikrishnan
author_facet Jain, Shubha
Swain, Sarpras
Das, Lopamudra
Swain, Sarita
Giri, Lopamudra
Kondapi, Anand Kumar
Narayanan Unni, Harikrishnan
author_sort Jain, Shubha
collection PubMed
description Tau protein aggregation is identified as one of the key phenomena associated with the onset and progression of Alzheimer’s disease. In the present study, we performed on-chip confocal imaging of tau protein aggregation and tau–drug interactions using a spiral-shaped passive micromixing platform. Numerical simulations and experiments were performed in order to validate the performance of the micromixer design. We performed molecular modeling of adenosine triphosphate (ATP)-induced tau aggregation in order to successfully validate the concept of helical tau filament formation. Tau aggregation and native tau restoration were realized using an immunofluorescence antibody assay. The dose–response behavior of an Alzheimer’s drug, methylthioninium chloride (MTC), was monitored on-chip for defining the optimum concentration of the drug. The proposed device was tested for reliability and repeatability of on-chip tau imaging. The amount of the tau protein sample used in our experiments was significantly less than the usage for conventional techniques, and the whole protein–drug assay was realized in less than two hours. We identified that intensity-based tau imaging could be used to study Alzheimer’s drug response. In addition, it was demonstrated that cell-free, microfluidic tau protein assays could be used as potential on-chip drug evaluation tools for Alzheimer’s disease.
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spelling pubmed-77633242020-12-27 Microfluidic Protein Imaging Platform: Study of Tau Protein Aggregation and Alzheimer’s Drug Response Jain, Shubha Swain, Sarpras Das, Lopamudra Swain, Sarita Giri, Lopamudra Kondapi, Anand Kumar Narayanan Unni, Harikrishnan Bioengineering (Basel) Communication Tau protein aggregation is identified as one of the key phenomena associated with the onset and progression of Alzheimer’s disease. In the present study, we performed on-chip confocal imaging of tau protein aggregation and tau–drug interactions using a spiral-shaped passive micromixing platform. Numerical simulations and experiments were performed in order to validate the performance of the micromixer design. We performed molecular modeling of adenosine triphosphate (ATP)-induced tau aggregation in order to successfully validate the concept of helical tau filament formation. Tau aggregation and native tau restoration were realized using an immunofluorescence antibody assay. The dose–response behavior of an Alzheimer’s drug, methylthioninium chloride (MTC), was monitored on-chip for defining the optimum concentration of the drug. The proposed device was tested for reliability and repeatability of on-chip tau imaging. The amount of the tau protein sample used in our experiments was significantly less than the usage for conventional techniques, and the whole protein–drug assay was realized in less than two hours. We identified that intensity-based tau imaging could be used to study Alzheimer’s drug response. In addition, it was demonstrated that cell-free, microfluidic tau protein assays could be used as potential on-chip drug evaluation tools for Alzheimer’s disease. MDPI 2020-12-13 /pmc/articles/PMC7763324/ /pubmed/33322166 http://dx.doi.org/10.3390/bioengineering7040162 Text en © 2020 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 (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Communication
Jain, Shubha
Swain, Sarpras
Das, Lopamudra
Swain, Sarita
Giri, Lopamudra
Kondapi, Anand Kumar
Narayanan Unni, Harikrishnan
Microfluidic Protein Imaging Platform: Study of Tau Protein Aggregation and Alzheimer’s Drug Response
title Microfluidic Protein Imaging Platform: Study of Tau Protein Aggregation and Alzheimer’s Drug Response
title_full Microfluidic Protein Imaging Platform: Study of Tau Protein Aggregation and Alzheimer’s Drug Response
title_fullStr Microfluidic Protein Imaging Platform: Study of Tau Protein Aggregation and Alzheimer’s Drug Response
title_full_unstemmed Microfluidic Protein Imaging Platform: Study of Tau Protein Aggregation and Alzheimer’s Drug Response
title_short Microfluidic Protein Imaging Platform: Study of Tau Protein Aggregation and Alzheimer’s Drug Response
title_sort microfluidic protein imaging platform: study of tau protein aggregation and alzheimer’s drug response
topic Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7763324/
https://www.ncbi.nlm.nih.gov/pubmed/33322166
http://dx.doi.org/10.3390/bioengineering7040162
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