Site-Directed Antibody Immobilization by Resorc[4]arene-Based Immunosensors.
immunosensor
macrocycles
resorc[4]arene
site directed immobilization
surface plasmon resonance
Journal
Chemistry (Weinheim an der Bergstrasse, Germany)
ISSN: 1521-3765
Titre abrégé: Chemistry
Pays: Germany
ID NLM: 9513783
Informations de publication
Date de publication:
08 Jul 2020
08 Jul 2020
Historique:
received:
24
02
2020
revised:
24
03
2020
pubmed:
3
4
2020
medline:
21
10
2020
entrez:
3
4
2020
Statut:
ppublish
Résumé
One of the main problems in the development of immunosensors is to overcome the complexity of binding antibodies to the sensor surface. Most immobilizing methods lead to a random orientation of antibodies with a lower binding site density and immunoaffinity. In order to control the orientation of antibody immobilization, several resorc[4]arene derivatives were designed and synthesized. After the spectroscopic characterization of resorc[4]arene self-assembled monolayers (SAMs) onto gold films, the surface coverage and the orientation of insulin antibody (Ab-Ins) were assessed by a surface plasmon resonance (SPR) technique and compared with a random immobilization method. Experimental results combined with theoretical studies confirmed the dipole-dipole interaction as an important factor in antibody orientation and demonstrated the importance of the upper rim functionalization of resorcarenes. Accordingly, resorcarene 5 showed a major binding force towards Ab-Ins thanks to the H-bond interactions with the amine protein groups. Based on these findings, the resorcarene-based immunosensor is a powerful system with improved sensitivity providing new insight into sensor development.
Identifiants
pubmed: 32240571
doi: 10.1002/chem.202000989
doi:
Substances chimiques
Antibodies
0
Antibodies, Immobilized
0
Gold
7440-57-5
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
8400-8406Subventions
Organisme : PON (Piano Operativo Nazionale)
ID : ARS01_00432 PROGEMA
Organisme : Ministero dell'Istruzione, dell'Università e della Ricerca
ID : PRIN 2017 - "Tar-geting Hedgehog pathway: Virtual screening identification and sustainable synthesis of novel Smo and Gli inhibitors and their pharmacological drug delivery strategies for im-proved therapeutic effects in tumors"
Organisme : Ministero dell'Istruzione, dell'Università e della Ricerca
ID : Dipartimenti di Eccellenza - L. 232/2016
Organisme : Sapienza Università di Roma
ID : project RM11816436113D8A
Organisme : Regione Lazio
ID : NanoBioPOCT25-OHD
Informations de copyright
© 2020 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.
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