Single-molecule conductance of double-stranded RNA oligonucleotides

RNA oligonucleotides are crucial for a range of biological functions and in many biotechnological applications. Herein, we measured, for the first time, the conductance of individual double-stranded (ds)RNA molecules and compared it with the conductance of single DNA:RNA hybrids. The average conductance values are similar for both biomolecules, but the distribution of conductance values shows an order of magnitude higher variability for dsRNA, indicating higher molecular flexibility of dsRNA. Microsecond Molecular Dynamics simulations explain this difference and provide structural insights into the higher stability of DNA:RNA duplex with the atomic level of detail. The rotations of 2’-OH groups of the ribose rings and the bases in RNA strands destabilize the duplex structure by weakening base stacking interactions, affecting charge transport, and making single-molecule conductance of dsRNA more variable (dynamic disorder). The results demonstrate that a powerful combination of state-of-the-art biomolecular electronics techniques and computational approaches can provide valuable insights into biomolecules’ biophysics with unprecedented spatial resolution.

The duplex structure of modern political extremism

The article focuses on the identification of common grounds in the system of political extremism and making a distinction between the goals pursued by its left- and right-wing directions. The main results: detection of the wide and narrow approaches to the interpretation of the definition of political extremism, synthesis of its universal features, authorial understanding of the category of political extremism, and identification of the unity and struggle of opposites in the essence of political extremism.

Microstructure and Mechanical Properties of High Relative Density γ-TiAl Alloy Using Irregular Pre-Alloyed Powder

Preparing high relative density γ-TiAl alloy by pressure-less sintering at low-cost has always been a challenge. Therefore, a new kind of non-spherical pre-alloyed TiAl powder was prepared by the reaction of TiH2 powder and Al powder at 800 °C to fabricate high-density Ti-48Al alloy via pressure-less sintering. The oxygen content was controlled to below 1800 ppm by using coarse Al powder (~120 μm). The sintered densities ranged from 92.1% to 97.5% with sintering temperature varying from 1300 °C to 1450 °C. The microstructure of the sintered compact was greatly influenced by the sintering temperature. The as-sintered samples had a near-γ structure at 1350 °C, a duplex structure at 1400 °C, and a nearly lamellar structure at 1450 °C. To achieve full densification, non-capsule hot isostatic pressing was performed on the 1350 °C and 1400 °C sintered samples. As a result, high compressive strengths of 2241 MPa and 1931MPa were obtained, which were higher than the existing Ti-48Al alloys.

Thermal Stability Changes in Telomeric G-Quadruplex Structures Due to N6-Methyladenine Modification

N6-methyladenine modification (m6dA) has recently been identified in eukaryote genomic DNA. The methylation destabilizes the duplex structure when the adenine forms a Watson–Crick base pair, whereas the methylation on a terminal unpaired adenine stabilizes the duplex structure by increasing the stacking interaction. In this study, the effects of m6dA modification on the thermal stability of four distinct telomeric G-quadruplex (G4) structures were investigated. The m6dA-modified telomeric oligonucleotide d[AGGG(TTAGGG)3] that forms a basket-type G4 in Na+, d[(TTAGGG)4TT] that forms a hybrid-type G4 in K+ (Form-2), d[AAAGGG(TTAGGG)3AA] that forms a hybrid-type G4 in K+ (Form-1), and d[GGG(TTAGGG)3T] that forms a basket-type G4 with two G-tetrads in K+ (Form-3) were analyzed. Circular dichroism melting analysis demonstrated that (1) A7- and A19-methylation destabilized the basket-type G4 structure that formed in Na+, whereas A13-methylation stabilized the structure; (2) A15-methylation stabilized the Form-2 G4 structure; (3) A15- and A21-methylations stabilized the Form-1 G4 structure; and (4) A12-methylation stabilized the Form-3 G4 structure. These results suggest that m6dA modifications may affect the thermal stability of human telomeric G4 structures in regulating the biological functions.