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This study aims to enhance the signal-to-noise ratio (SNR) in chemiluminescence immunoassays (CLIA) by increasing the protein immobilization capacity on magnetic bead surfaces. Proteins are macromolecules with three-dimensional conformations where merely increasing the density of surface functional groups on magnetic beads is insufficient to substantially enhance protein immobilization. To address this limitation, we grafted polyamidoamine (PAMAM) dendrimers with three-dimensional architectures onto magnetic beads, simultaneously augmenting the functional group density and expanding the spatial distribution to improve protein loading capacity. PAMAMs were synthesized via iterative Michael addition and amidation cycles between ethylenediamine and methyl acrylate, with its grafting density and behavior on magnetic beads characterized by nuclear magnetic resonance (NMR) spectroscopy. Dynamic light scattering (DLS) analysis revealed an increased hydrodynamic radius of the PAMAM-grafted beads, confirming the successful expansion of protein-binding spatial domains. We investigated the impact of PAMAM grafting on the immobilization efficiency of bovine serum albumin (BSA) and mouse immunoglobulin G (IgG). Experimental results demonstrated that PAMAM grafting enhanced the protein immobilization capacity from 11.5 to 33.5 mg/g for BSA and from 8.3 to 19.2 mg/g for IgG, representing 2.9-fold and 2.3-fold improvements, respectively. The SNR improvement was evaluated by using a CLIA-based detection system for the creatine kinase-MB (CK-MB) biomarker. PAMAM grafting achieved 7.21-fold and 4.79-fold improvements in low-to-background and high-to-background ratios and reduced the limits of detection (LOD) from 52.58 to 7.73 pg/mL, respectively, and the optimized LOD fully meets the clinical sensitivity requirements for detecting CK-MB. This work demonstrates that grafting three-dimensional PAMAM dendrimer effectively enhances protein immobilization on magnetic beads, significantly improving CLIA SNR, thereby providing a novel strategy for optimizing immunoassay performance.
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http://dx.doi.org/10.1021/acs.langmuir.5c03451 | DOI Listing |
Protein Expr Purif
September 2025
Key Laboratory of Enzyme and Protein Technology, VNU University of Science, Vietnam National University, Hanoi, 334 Nguyen Trai, Thanh Xuan, Hanoi, Vietnam; Faculty of Biology, VNU University of Science, Vietnam National University, Hanoi, 334 Nguyen Trai, Thanh Xuan, Hanoi, Vietnam. Electronic addr
The 3C-like protease (3CLpro) of SARS-CoV-2 is a crucial target for antiviral drugs due to its essential role in viral polyprotein processing. In this study, we designed and produced a modular fluorescent recombinant substrate (6×His-ECFP-AVLQSGFRK-EYFP), which was then immobilized on Ni-NTA magnetic beads (Ni-NTA-6×His-ECFP-AVLQSGFRK-EYFP) for the assay of 3CLpro activity. Upon cleavage at the specific AVLQ↓SG motif, the EYFP fragment was released into the supernatant and quantified via fluorescence measurement (Ex/Em = 480/528 nm).
View Article and Find Full Text PDFTalanta
August 2025
School of Public Health &Jiangxi Provincial Key Laboratory of Disease Prevention and Public Health, Jiangxi Medical College, Nanchang University, Nanchang, Jiangxi, 330031, PR China. Electronic address:
Hemorrhagic fever with renal syndrome (HFRS), caused by Hantaan virus, poses a serious public health threat. Current diagnostic methods remain limited by low sensitivity, complex procedures, and high sample requirements. To address this, we developed a highly sensitive single-molecule biosensor using multi-fluorophore nucleic acid probes and STORM imaging for the detection of Hantaan virus RNA.
View Article and Find Full Text PDFSci Bull (Beijing)
August 2025
Key Laboratory for Micro/Nano Optoelectronic Devices of Ministry of Education & Hunan Provincial Key Laboratory of Low-Dimensional Structural Physics and Devices, School of Physics and Electronics, Hunan University, Changsha 410082, China. Electronic address:
Determining the number of photons in an incident light pulse at room temperature is the ultimate goal of photodetection. Herein, we report a plasmon-strain-coupled tens of photon level phototransistor by integrating monolayer MoS on top of Au nanowire (NW). Within this structure, Au NW can greatly enhance incident light intensity around MoS, and the large tensile strain can reduce the contact energy barrier between MoS and Au NW, so as to achieve efficient injection of plasmonic hot electrons into MoS.
View Article and Find Full Text PDFAnal Chim Acta
October 2025
Department of Chemistry, Federal University of São Carlos-UFSCar, Rod. Washington Luís km 235 - São Carlos, SP, 13565-905, Brazil. Electronic address:
Background: Magnetic particles (MPs) are widely used in bioanalytical systems to quickly separate specific targets from complex samples using a magnetic field. MPs can be easily functionalized with bioreceptors to capture, separate, and concentrate biomarkers like proteins, oligonucleotides, and cells. Combining MPs-separation capabilities with electrochemical sensors can greatly enhance the sensitivity of these devices, helping achieve ultralow limits of detection for biomarkers.
View Article and Find Full Text PDFAnal Chem
August 2025
Department of Chemical Sciences, University of Catania, Viale Andrea Doria 6, 95125 Catania, Italy.
In vitro fertilization (IVF) faces challenges in evaluating embryo quality and in determining the genetic health of embryos. Key biomarkers in the culture medium, including nucleic acids and proteins, offer promising avenues for noninvasive assessment. However, small sample volumes, low biomolecule concentrations, and potential contaminants complicate the reliable detection of genetic indicators.
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