Tuning Surface Plasmon Resonance Responses through Size and Crosslinking Control of Multivalent Protein Binding-Capable Nanoscale Hydrogels
- 6 June 2022
- journal article
- research article
- Published by American Chemical Society (ACS) in ACS Biomaterials Science & Engineering
- Vol. 8 (7) , 2878-2889
Abstract
Surface plasmon resonance (SPR) phenomena have been widely studied to detect biomolecules because of their high sensitivity and ability to determine biomolecular interactions with kinetic information. However, highly selective detection in specific concentration ranges relevant to target biomolecules is still a challenging task. Recently, we developed bioresponsive nanoscale hydrogels to selectively intensify SPR signals through multivalent protein binding (MPB) events with target biomolecules, including IL-2, where we were able to demonstrate exceptional selectivity for target biomolecules with minimal responses to nonspecific and monovalent binding events. In this work, we systematically explored the relationship between the physical properties of MPB-capable nanoscale hydrogels and their SPR response induced in the presence of the programmed cell death protein 1 antibody (PD-1Ab) as a model target biomolecule. First, we developed a synthetic protocol by controlling various reaction parameters to construct a library of nanoscale poly(N-isopropylacrylamide-co-acrylic acid) hydrogels (NHs) with different sizes (from 400 nm to 1 μm) and degrees of crosslinking (from 2 to 8%). Then, by incorporating MPB-capable PD-1 receptors onto the surface of NHs to form PD-1-responsive nanoscale hydrogels (PNHs), the hydrogel size and crosslinking dependency of their SPR responses were investigated. Our results reveal the appropriate hydrogel size regime and degree of crosslinking for effective PD-1Ab detection at specific concentrations range between a few nM and 1 μM. Overall, our study demonstrates that by tuning the physical properties of the nanoscale hydrogel matrix, the sensitivity and detection range of MPB-based SPR sensors can be modulated to potentially benefit clinical applications such as monitoring diverse therapeutic biomolecules.Keywords
Funding Information
- National Research Foundation of Korea (NRF-2018M3A7B4071204, NRF-2019R1I1A1A01057356, NRF2018R1D1A1A02086125)
- Ministry of Health & Welfare of Korea (HR14C0007, HV20C0054)
- Research Resettlement Fund for new faculty of Seoul National University
This publication has 49 references indexed in Scilit:
- Active Control of SPR by Thermoresponsive Hydrogels for Biosensor ApplicationsThe Journal of Physical Chemistry C, 2013
- A Simple Point-of-Care Microfluidic Immunomagnetic Fluorescence Assay for PathogensAnalytical Chemistry, 2013
- Safety, Activity, and Immune Correlates of Anti–PD-1 Antibody in CancerNew England Journal of Medicine, 2012
- Semibatch emulsion copolymerization of butyl acrylate and glycidyl methacrylate: Effect of operating variablesJournal of Applied Polymer Science, 2010
- Synthesis of multifunctional nanogels using a protected macromonomer approachColloid and Polymer Science, 2008
- Size-controlled synthesis of monodisperse core/shell nanogelsColloid and Polymer Science, 2007
- Influence of Ancillary Binding and Nonspecific Adsorption on Bioresponsive Hydrogel MicrolensesBiomacromolecules, 2007
- Preparation and Characterization of Photo-Cross-Linked Thermosensitive PNIPAAm NanogelsMacromolecules, 2006
- Influence of Reaction Conditions on the Synthesis of Self-Cross-Linked N-Isopropylacrylamide MicrogelsLangmuir, 2003
- Uniform polymer particles by dispersion polymerization in alcoholJournal of Polymer Science Part A: Polymer Chemistry, 1986