Fluorescence Masking Based Multifunctional Quantum Dots’ Assay for HSP90α Interactions Detection

Research output: Contribution to journalArticleResearchpeer review

Authors

  • Anusha Kishore
  • Lu Fan
  • Frank Stahl
  • Thomas Reichel
  • Karsten Krüger
  • Carsten Zeilinger

External Research Organisations

  • Justus Liebig University Giessen
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Details

Original languageEnglish
Article number2957
JournalApplied Sciences (Switzerland)
Volume13
Issue number5
Publication statusPublished - 25 Feb 2023

Abstract

Featured Application: The quantum dots-based assay described here uses fluorescence masking to detect protein–ligand and protein–protein interactions on a glass slide in a multifunctional way. This is used here for the stress protein HSP90α in purified form and in cell lysate. It can be further used for other different proteins. HSP90α is one of the most common stress proteins in cells; hence, it is a good target for developing drugs and testing systems for cancer or physical stress levels in humans. Streptavidin conjugated quantum dots (Sav-QDs) are widely used as fluorophores for biosensing to overcome chemical labelling problems. In this work, we have attempted to develop a multifunctional and robust assay for HSP90α. The detection technique was based on the masking of the fluorescence of spotted Sav-QDs on nitrocellulose chips (NC). Biotinylated ligand/antibody attaches to the spotted Sav-QD and then HSP90α is attached, which causes the masking of fluorescence. The masking of fluorescence was used to detect protein–ligand interactions, the effect of inhibitors, protein–protein interactions, and the presence of protein in the biological sample. The load of detection (LoD) of the assay lies in the nano molar range, making it a sensitive assay. The results from the experiments suggest that the used approach is promising for developing a multifunctional, robust, and sensitive assay for proteins that can be used for point-of-care detection in complex biological samples.

Keywords

    biotin-ATP, biotin-HSP90 antibody, fluorescence masking, HSP90α, quantum dots, Sav-QD

ASJC Scopus subject areas

Sustainable Development Goals

Cite this

Fluorescence Masking Based Multifunctional Quantum Dots’ Assay for HSP90α Interactions Detection. / Kishore, Anusha; Fan, Lu; Stahl, Frank et al.
In: Applied Sciences (Switzerland), Vol. 13, No. 5, 2957, 25.02.2023.

Research output: Contribution to journalArticleResearchpeer review

Kishore A, Fan L, Stahl F, Reichel T, Krüger K, Zeilinger C. Fluorescence Masking Based Multifunctional Quantum Dots’ Assay for HSP90α Interactions Detection. Applied Sciences (Switzerland). 2023 Feb 25;13(5):2957. doi: 10.3390/app13052957
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abstract = "Featured Application: The quantum dots-based assay described here uses fluorescence masking to detect protein–ligand and protein–protein interactions on a glass slide in a multifunctional way. This is used here for the stress protein HSP90α in purified form and in cell lysate. It can be further used for other different proteins. HSP90α is one of the most common stress proteins in cells; hence, it is a good target for developing drugs and testing systems for cancer or physical stress levels in humans. Streptavidin conjugated quantum dots (Sav-QDs) are widely used as fluorophores for biosensing to overcome chemical labelling problems. In this work, we have attempted to develop a multifunctional and robust assay for HSP90α. The detection technique was based on the masking of the fluorescence of spotted Sav-QDs on nitrocellulose chips (NC). Biotinylated ligand/antibody attaches to the spotted Sav-QD and then HSP90α is attached, which causes the masking of fluorescence. The masking of fluorescence was used to detect protein–ligand interactions, the effect of inhibitors, protein–protein interactions, and the presence of protein in the biological sample. The load of detection (LoD) of the assay lies in the nano molar range, making it a sensitive assay. The results from the experiments suggest that the used approach is promising for developing a multifunctional, robust, and sensitive assay for proteins that can be used for point-of-care detection in complex biological samples.",
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note = "Funding Information: The project was funded by the German Federal Institute of Sport Science (Bundesinstitut f{\"u}r Sportwissenschaft, BISP), project {\textquoteleft}Definition of valid and reliable biomarkers including innovative measurement methods for training control in long-distance running{\textquoteright} (grant number 070503/20-21. Funding Information: We would like to acknowledge Institute of Technical Chemistry, Gottfried-Wilhelm-Leibniz University Hannover for providing infrastructural support and Department of Exercise Physiology and Sports Therapy, Institute of Sports Science, JUSTUS-LIEBIG University, Giessen, Germany, for providing materialistic and financial support. ",
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AU - Kishore, Anusha

AU - Fan, Lu

AU - Stahl, Frank

AU - Reichel, Thomas

AU - Krüger, Karsten

AU - Zeilinger, Carsten

N1 - Funding Information: The project was funded by the German Federal Institute of Sport Science (Bundesinstitut für Sportwissenschaft, BISP), project ‘Definition of valid and reliable biomarkers including innovative measurement methods for training control in long-distance running’ (grant number 070503/20-21. Funding Information: We would like to acknowledge Institute of Technical Chemistry, Gottfried-Wilhelm-Leibniz University Hannover for providing infrastructural support and Department of Exercise Physiology and Sports Therapy, Institute of Sports Science, JUSTUS-LIEBIG University, Giessen, Germany, for providing materialistic and financial support.

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