Cupredoxin engineered upconversion nanoparticles for ratiometric luminescence sensing of Cu2+. Issue 7 (24th May 2019)
- Record Type:
- Journal Article
- Title:
- Cupredoxin engineered upconversion nanoparticles for ratiometric luminescence sensing of Cu2+. Issue 7 (24th May 2019)
- Main Title:
- Cupredoxin engineered upconversion nanoparticles for ratiometric luminescence sensing of Cu2+
- Authors:
- Liu, Chang
Yu, Yingjie
Chen, Daquan
Zhao, Jian
Yu, Yang
Li, Lele
Lu, Yi - Abstract:
- Abstract : The integration of zwitterion-coated UCNPs with azurin, a member of a family of redox-active copper proteins, can serve as an ideal platform for the label-free upconversion luminescence sensing of Cu 2+ with a ratiometric response. Abstract : The NIR excitation and large anti-Stokes shift of upconversion nanoparticles (UCNPs) have made them an ideal choice as biological nanoprobes. A key challenge in the field is to confer biorecognition units to UCNPs so that they can be used to probe specific targets in biological systems. While various agents have been combined with UCNPs to meet such a challenge, most studies are limited to small molecules, while biomolecules such as metalloproteins that possess much higher affinity and selectivity for metal ions have not been explored. Herein we demonstrate that fusion of zwitterion-coated UCNPs with azurin, a member of a family of redox-active copper proteins called cupredoxins that play important roles in diverse biological functions, can serve as an ideal platform for the label-free upconversion luminescence sensing of Cu 2+ with a ratiometric response. The selective binding of apo-azurin with Cu 2+ induces a significant absorbance at about 625 nm, and hence decreases the red emission of the UCNPs. In contrast, the green emission of the UCNPs remains constant and acts as an internal standard reference for the ratiometric sensing of Cu 2+ . This approach opens a new window for the development of assays for biosensing basedAbstract : The integration of zwitterion-coated UCNPs with azurin, a member of a family of redox-active copper proteins, can serve as an ideal platform for the label-free upconversion luminescence sensing of Cu 2+ with a ratiometric response. Abstract : The NIR excitation and large anti-Stokes shift of upconversion nanoparticles (UCNPs) have made them an ideal choice as biological nanoprobes. A key challenge in the field is to confer biorecognition units to UCNPs so that they can be used to probe specific targets in biological systems. While various agents have been combined with UCNPs to meet such a challenge, most studies are limited to small molecules, while biomolecules such as metalloproteins that possess much higher affinity and selectivity for metal ions have not been explored. Herein we demonstrate that fusion of zwitterion-coated UCNPs with azurin, a member of a family of redox-active copper proteins called cupredoxins that play important roles in diverse biological functions, can serve as an ideal platform for the label-free upconversion luminescence sensing of Cu 2+ with a ratiometric response. The selective binding of apo-azurin with Cu 2+ induces a significant absorbance at about 625 nm, and hence decreases the red emission of the UCNPs. In contrast, the green emission of the UCNPs remains constant and acts as an internal standard reference for the ratiometric sensing of Cu 2+ . This approach opens a new window for the development of assays for biosensing based on a combination of specific metalloproteins with UCNPs. … (more)
- Is Part Of:
- Nanoscale advances. Volume 1:Issue 7(2019)
- Journal:
- Nanoscale advances
- Issue:
- Volume 1:Issue 7(2019)
- Issue Display:
- Volume 1, Issue 7 (2019)
- Year:
- 2019
- Volume:
- 1
- Issue:
- 7
- Issue Sort Value:
- 2019-0001-0007-0000
- Page Start:
- 2580
- Page End:
- 2585
- Publication Date:
- 2019-05-24
- Subjects:
- 620.5
- Journal URLs:
- http://pubs.rsc.org/en/journals/journalissues/na#!recentarticles&adv ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/c9na00168a ↗
- Languages:
- English
- ISSNs:
- 2516-0230
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 12675.xml