Dimeric Human β‑Defensin 3 as a Universal Platform for Intracellular Delivery of Nucleic Acid Cargos

Functional nucleic acids including siRNA, mRNA, and plasmid DNA are promising bioactive molecules to regulate cellular functions uncontrollable by conventional small molecule regulators. To realize successful cellular applications of these nucleic acids, an intracellular gene delivery vehicle with high efficiency and low cytotoxicity is required. Here, we report the dimerization of human β-defensin 3 (DhBD3) promoted by the interaction between β-strands and the application of DhBD3 for efficient delivery of various nucleic acid cargos. DhBD3 with multiple cationic residues could be complexed with various types of polyanionic DNA and RNA. DhBD3 could intracellularly deliver both small and large nucleic acid cargos loaded by complexation to regulate the expression level of target proteins, showing its potential as a universal platform for nucleic acid delivery. In addition, as DhBD3 is a human-derived material with high biocompatibility and can be robustly prepared by an inexpensive method, it is a promising gene delivery system that can be employed for biomedical purposes

Influence of Cation Substitutions Based on ABO₃ Perovskite Materials, Sr_1–<i>x</i>Y_<i>x</i>Ti_1–<i>y</i>Ru_<i>y</i>O_3−δ, on Ammonia Dehydrogenation

In order to screen potential catalytic materials for synthesis and decomposition of ammonia, a series of ABO₃ perovskite materials, Sr_1–<i>x</i>Y_<i>x</i>Ti_1–<i>y</i>Ru_<i>y</i>O_3−δ (<i>x</i> = 0, 0.08, and 0.16; <i>y</i> = 0, 0.04, 0.07, 0.12, 0.17, and 0.26) were synthesized and tested for ammonia dehydrogenation. The influence of A or B site substitution on the catalytic ammonia dehydrogenation activity was determined by varying the quantity of either A or B site cation, producing <b>Sr</b>_{<b>1</b>–<b><i>x</i></b>}<b>Y</b>_{<b><i>x</i></b>}Ti_0.92Ru_0.08O_3−δ and Sr_0.92Y_0.08<b>Ti</b>_{<b>1</b>–<i><b>y</b></i>}<b>Ru</b>_{<b><i>y</i></b>}O_3−δ, respectively. Characterizations of the as-synthesized materials using different analytical techniques indicated that a new perovskite phase of SrRuO₃ was produced upon addition of large amounts of Ru (≥12 mol %), and the surface Ru⁰ species were formed simultaneously to ultimately yield <b>Ru</b>_{<b><i>z</i></b>}(surface)/Sr_0.92Y_0.08<b>Ti</b>_{<b>1</b>–<b><i>y</i></b>}<b>Ru</b>_{<i><b>y</b></i>–<b><i>z</i></b>}O_3−δ and/or <b>Ru</b>_{<b><i>z</i></b>–<b><i>w</i></b>}(surface)/Sr_<i>w</i>Ru_<i>w</i>O₃/Sr_{0.92–<i>w</i>}Y_0.08<b>Ti</b>_{<b>1</b>–<b><i>y</i></b>}<b>Ru</b>_{<b><i>y</i></b>–<b><i>z</i></b>}O_3−δ. The newly generated surface Ru⁰ species at the perovskite surfaces accelerated ammonia dehydrogenation under different conditions, and Sr_0.84Y_0.16Ti_0.92Ru_0.08O_3−δ exhibited a NH₃ conversion of ca. 96% at 500 °C with a gas hourly space velocity (GHSV) of 10 000 mL g_cat^–1 h^–1. In addition, Sr_0.84Y_0.16Ti_0.92Ru_0.08O_3−δ further proved to be highly active and stable toward ammonia decomposition at different reaction temperatures and GHSVs for >275 h