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Kavalnyte, E.

Publications and source records attributed to Kavalnyte, E..

2 recordsLinked to original sources

Electrophysiological properties and synaptic activity of the mouse hippocampal CA1 neurons during postnatal development

Early postnatal development is a critical period for hippocampal circuit maturation. While postnatal hippocampal development has been mostly studied in rats, less is known about the developmental trajectory of electrophysiological properties in mice, despite the wide use of these animal models for molecular and genetic studies of nervous system. In this study, we investigated the postnatal maturation of hippocampal CA1 pyramidal neurons in male and female wild-type mice. Whole-cell patch-clamp recordings were performed in acute hippocampal slices to assess passive and active membrane properties as well as spontaneous excitatory synaptic activity. We found that maturation of neuronal firing properties was associated with faster responses to stimulation, higher-amplitude and shorter-duration action potentials, and more precise control of neuronal firing. Simultaneously, synaptic activity changed across development, with decreased sEPSC inter-event intervals and stable event amplitudes, suggesting enhanced functional connectivity without major changes in synaptic strength. Sex-dependent differences in electrophysiological properties were observed primarily during the first postnatal week, indicating that sex influences the early trajectory of neuronal maturation. Together, our findings provide a comprehensive electrophysiological baseline for mouse hippocampal CA1 pyramidal neurons during postnatal development.

biophysics↗

β-Barrel domain swapping in α-hemolysin enables enhanced single-molecule biomolecule sensing

Biological nanopores are powerful platforms for single-molecule analysis, yet rational strategies to tune their transport and sensing properties remain limited. Here we present a modular engineering approach based on {beta}-barrel domain swapping to reprogram the function of the prototypical nanopore -hemolysin. By replacing its native {beta}-barrel with {beta}-barrel domains from diverse pore-forming toxins, we generate a series of chimera nanopores that retain oligomerization capability while exhibiting reduced membrane-permeabilizing activity. Electrophysiological measurements show that selected chimera pores form stable, conductive channels with distinct ion transport properties. Notably, the HL_NetB chimera displays stable conductance, enhanced electroosmotic flow, and improved performance in nucleic acid and protein sensing. Single-molecule experiments demonstrate that this chimera markedly slows the translocation of single-stranded DNA, enabling discrimination by length and sequence, improves the resolution of intrinsically disordered proteins such as -synuclein, and enhances sensitivity to RNA conformational changes. Together, these results establish {beta}-barrel domain swapping as a general and effective strategy for engineering biological nanopores with tailored single-molecule sensing capabilities.

biochemistry↗