Highly robust and optimized conjugation of antibodies to nanoparticles using quantitatively validated protocols. Issue 7 (2nd February 2017)
- Record Type:
- Journal Article
- Title:
- Highly robust and optimized conjugation of antibodies to nanoparticles using quantitatively validated protocols. Issue 7 (2nd February 2017)
- Main Title:
- Highly robust and optimized conjugation of antibodies to nanoparticles using quantitatively validated protocols
- Authors:
- Jeong, Sinyoung
Park, Ji Yong
Cha, Myeong Geun
Chang, Hyejin
Kim, Yong-il
Kim, Hyung-Mo
Jun, Bong-Hyun
Lee, Dong Soo
Lee, Yoon-Sik
Jeong, Jae Min
Lee, Yun-Sang
Jeong, Dae Hong - Abstract:
- Abstract : The click chemistry-based antibody conjugation strategy offers proper orientation of the target binding sites in antibodies on nanoparticles (NPs) and a high density of antibodies per single NP, while preserving the intact target-binding capability. Abstract : Antibody-conjugated nanoparticles (NPs) have attracted great attention in diagnostic and therapeutic applications due to their high sensitivity and specificity for biotargets, as well as their wide applicability. Unfortunately, these features are significantly affected by antibody conjugation methods in terms of conjugation efficiency, orientation of the target binding site in the antibody, and denaturation during chemical conjugation reactions. Furthermore, the number of conjugated antibodies on each NP and the overall targeting efficacy are critical factors for a quantitative bioassay with antibody-conjugated NPs. Herein, we report a versatile and oriented antibody conjugation method using copper-free click chemistry. Moreover, the number of conjugated antibodies and their binding capacity were quantitatively and experimentally evaluated using fluorescently-labeled antibodies and antigens. The strong binding capability of antibody-conjugated NPs prepared using the copper-free click chemistry-based conjugation strategy was 8 times superior to the binding capability seen following the use of the EDC/NHS-coupling method. Additionally, the versatility of the developed antibody conjugation method was alsoAbstract : The click chemistry-based antibody conjugation strategy offers proper orientation of the target binding sites in antibodies on nanoparticles (NPs) and a high density of antibodies per single NP, while preserving the intact target-binding capability. Abstract : Antibody-conjugated nanoparticles (NPs) have attracted great attention in diagnostic and therapeutic applications due to their high sensitivity and specificity for biotargets, as well as their wide applicability. Unfortunately, these features are significantly affected by antibody conjugation methods in terms of conjugation efficiency, orientation of the target binding site in the antibody, and denaturation during chemical conjugation reactions. Furthermore, the number of conjugated antibodies on each NP and the overall targeting efficacy are critical factors for a quantitative bioassay with antibody-conjugated NPs. Herein, we report a versatile and oriented antibody conjugation method using copper-free click chemistry. Moreover, the number of conjugated antibodies and their binding capacity were quantitatively and experimentally evaluated using fluorescently-labeled antibodies and antigens. The strong binding capability of antibody-conjugated NPs prepared using the copper-free click chemistry-based conjugation strategy was 8 times superior to the binding capability seen following the use of the EDC/NHS-coupling method. Additionally, the versatility of the developed antibody conjugation method was also demonstrated by conjugation of the antibody to three kinds of silica-encapsulated NPs. … (more)
- Is Part Of:
- Nanoscale. Volume 9:Issue 7(2017)
- Journal:
- Nanoscale
- Issue:
- Volume 9:Issue 7(2017)
- Issue Display:
- Volume 9, Issue 7 (2017)
- Year:
- 2017
- Volume:
- 9
- Issue:
- 7
- Issue Sort Value:
- 2017-0009-0007-0000
- Page Start:
- 2548
- Page End:
- 2555
- Publication Date:
- 2017-02-02
- Subjects:
- Nanoscience -- Periodicals
Nanotechnology -- Periodicals
620.505 - Journal URLs:
- http://www.rsc.org/Publishing/Journals/NR/Index.asp ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/c6nr04683e ↗
- Languages:
- English
- ISSNs:
- 2040-3364
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 9830.266000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 1148.xml