The detection and identification of nanoscale molecules are crucial, but traditional technology comes with a high cost and requires skilled operators. Solid-state nanopores are new powerful tools for discerning the three-dimensional shape and size of molecules, enabling the translation of molecular structural information into electric signals. Here, DNA molecules with different shapes were designed to explore the effects of electroosmotic forces (EOF), electrophoretic forces (EPF), and volume exclusion on electric signals within solid-state nanopores. Our results revealed that the electroosmotic force was the main driving force for single-stranded DNA (ssDNA), whereas double-stranded DNA (dsDNA) was primarily dominated by electrophoretic forces in nanopores. Moreover, dsDNA caused greater amplitude signals and moved faster through the nanopore due to its larger diameter and carrying more charges. Furthermore, at the same charge level and amount of bases, circular dsDNA exhibited a tighter structure compared to brush DNA, resulting in a shorter length. Consequently, circular dsDNA caused higher current-blocking amplitudes and faster passage speeds. The characterization approach based on nanopores allows researchers to get molecular information about size and shape in real time. These findings suggest that nanopore detection has the potential to streamline nanoscale characterization and analysis, potentially reducing both the cost and complexity.
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http://dx.doi.org/10.1021/acs.langmuir.4c00401 | DOI Listing |
Anal Chem
March 2025
Department of Electrical Engineering, Pennsylvania State University, University Park, Pennsylvania 16802, United States.
Loop-mediated isothermal amplification (LAMP) is a promising method for point-of-care nucleic acid testing due to its simplicity, rapidity, and high sensitivity. Coupling LAMP with solid-state nanopores enables label-free, single-molecule sensing, enhancing diagnostic accuracy. However, conventional LAMP-coupled nanopore protocols require high-salt buffers (>1 M) to improve signal strength and translocation frequency, complicating workflows and increasing contamination risks.
View Article and Find Full Text PDFBiosens Bioelectron
February 2025
School of Biomedical and Pharmaceutical Sciences, Guangdong University of Technology, Guangzhou, Guangdong, China; Guangdong Provincial Key Laboratory of Research on Emergency in TCM, Guangzhou, Guangdong, China; Chinese Medicine Guangdong Laboratory, Zhuhai, Guangdong, China. Electronic address:
Nanopore technology is a promising single-molecule sensing platform that can identify substances through the precise monitoring of changes in ion currents. However, protein detection in clinical samples using solid-state nanopores remains challenging due to their heterogeneously charged spherical structure, which results in signals with extremely low signal-to-noise ratios (SNR) and low capture rates that are difficult to analyze. In this study, we employed a double-antibody sandwich technique to specifically capture and amplify the target antigen, which significantly improves the SNR and effectively distinguishes the target signal from background interference.
View Article and Find Full Text PDFInorg Chem
March 2025
Guizhou Key Laboratory of Macrocyclic and Supramolecular Chemistry, Guizhou University, Guiyang 550025, China.
The design and preparation of super proton conducting metal-organic frameworks (MOFs) are of great significance for the advancement of proton exchange membrane fuel cells (PEMFCs). An effective approach to increase the sulfonic acid density and control the hydrogen bonding networks within MOFs involves incorporating polymer chains that contain sulfonic acid groups into their pore structures. In this work, we report the synthesis of a polyvinyl sulfonic acid (PVS) cross-linked polymer within the nanopores of MIL-101-SOH, resulting in the PVS@MIL-101-SOH composite.
View Article and Find Full Text PDFAnalyst
March 2025
State Key Laboratory of Digital Medical Engineering, School of Biological Science and Medical Engineering, Southeast University, Nanjing, 210096, China.
Solid-state nanopores represent a powerful platform for the detection and characterization of a wide range of biomolecules and particles, including proteins, viruses, and nanoparticles, for clinical and biochemical applications. Typically, nanopores operate by measuring transient pulses of ionic current during translocation events of molecules passing through the pore. Given the strong noise and stochastic fluctuations in ionic current recordings during nanopore experiments, signal processing based on the statistical analysis of numerous translocation events remains a crucial issue for nanopore sensing.
View Article and Find Full Text PDFSci Adv
February 2025
Department of Chemical and Environmental Engineering, Yale University, New Haven, CT 06520-8286, USA.
As the gap between lithium supply and demand continues to widen, the need to develop ion-selective technologies, which can efficiently extract lithium from unconventional water sources, grows increasingly crucial. In this study, we investigated the fundamentals of applying a solid-state electrolyte (SSE), typically used in battery technologies, as a membrane material for aqueous lithium extraction. We find that the anhydrous hopping of lithium ions through the ordered and confined SSE lattice is highly distinct from ion migration through the hydrated free volumes of conventional nanoporous membranes, thus culminating in unique membrane transport properties.
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