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(Reference retrieved automatically from Web of Science through information on FAPESP grant and its corresponding number as mentioned in the publication by the authors.)

Peptide-Conjugated Silver Nanoparticle for Autoantibody Recognition

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Author(s):
Higa, Akemi M. [1, 2] ; Mambrini, Giovanni P. [2] ; Ierich, Jessica C. M. [1, 2] ; Garcia, Pamela S. [1, 2] ; Scramin, Juliana A. [2] ; Peroni, Luis A. [3] ; Okuda-Shinagawa, Nancy M. [4] ; Machini, M. Teresa [4] ; Trivinho-Strixino, Francisco [2] ; Leite, Fabio L. [2]
Total Authors: 10
Affiliation:
[1] Univ Sao Paulo, Inst Trop Med, BR-05403000 Sao Paulo - Brazil
[2] Univ Fed Sao Carlos, Dept Chem Phys & Math, BR-18052780 Sorocaba - Brazil
[3] Rheabiotech Lab Res & Dev, BR-13084791 Campinas, SP - Brazil
[4] Univ Sao Paulo, Inst Chem, Dept Biochem, BR-05508000 Sao Paulo - Brazil
Total Affiliations: 4
Document type: Journal article
Source: Journal of Nanoscience and Nanotechnology; v. 19, n. 12, p. 7564-7573, DEC 2019.
Web of Science Citations: 3
Abstract

In this work, we considered the autoantibodies proposed as putative biomarkers of demyelination taking into account their reactivity towards myelin oligodendrocyte glycoprotein (MOG) and myelin basic protein (MBP). These myelin proteins are among the most commonly researched targets in the immunopathology of demyelinating diseases. In this context, the development of assays for autoantibody detection can contribute as a predictive value for the early diagnosis of demyelinating diseases. Hence, we aimed to address the application of silver nanoparticles (AgNPs) as a sensing device of autoantibodies. AgNPs were synthesized via a chemical reduction method and characterized using atomic force microscopy (AFM), X-ray diffractometry, dynamic light scattering, and UV-visible spectrophotometry. The process of peptide conjugation on the nanoparticles was also analyzed. The autoantibody recognition by the peptide-conjugated AgNPs was evaluated with UV-visible spectrophotometry, atomic force spectroscopy (AFS), and color changing. AgNPs exhibited spherical morphology, low polydispersity, face-centered cubic crystal structure, and an average size of 29.3 +/- 3.0 nm. The hydrodynamic diameter variation and AFM showed that the MBP peptide induced greater agglomeration, compared to MOG peptide. The AFS measurements indicated the efficient binding of peptides to the AgNPs maintaining their activity, revealed by typical adhesion force and shapes of curves. The absorption spectrum features were more affected by the interaction with the specific autoantibodies, which also caused a visible color change in suspension providing a qualitative response. We described a preliminary study of MOG- and MBP-conjugated AgNPs which showed to be applicable in the autoantibody recognition. These have promising implication in the searching for biological markers for diagnostic purposes in the demyelination context, in which the nanoscale sensing exploitation is recent. (AU)

FAPESP's process: 14/12082-4 - Molecular modeling of the antigen-antibody complex to the investigations of autoimmune demyelinating diseases
Grantee:Jéssica Cristiane Magalhães Ierich
Support type: Scholarships in Brazil - Doctorate
FAPESP's process: 15/06847-0 - Synthesis and characterization of silver nanoparticles applied to immunoglobulins G detection
Grantee:Akemi Martins Higa
Support type: Scholarships in Brazil - Master
FAPESP's process: 14/21530-0 - Imnunonanosensors based on atomic force microscopy for multiple sclerosis studies
Grantee:Pâmela Soto Garcia
Support type: Scholarships in Brazil - Doctorate
FAPESP's process: 10/10813-0 - Preparation of nanostructures oxides films using electrochemical methods for sensor purposes
Grantee:Francisco Trivinho Strixino
Support type: Research Grants - Young Investigators Grants