Switchable multi-functional broadband polarization converter in terahertz band.

In this work, we propose a multi-functional broadband terahertz polarization converter based on graphene-VO hybrid metamaterial, which can switch between transmissive linear-to-linear conversion and reflective linear-to-circular conversion. The function of the metamaterial can be controlled by both the temperature and the Fermi energy of the graphene. At 298K, the metamaterial converts the y-polarized wave into x-polarized wave in 0.

Function switchable broadband wave plate based on the Au-VO hybrid metasurface.

In recent years, the integration of active materials into a metasurface to achieve tunable devices has attracted much attention. Here, we design an Au-VO hybrid metasurface, which can switch between quarter-wave plate and half-wave plate due to the phase transition of VO. At 298 K, the proposed structure acts as a quarter-wave plate in the 0.

Molecular basis for hierarchical histone de-β-hydroxybutyrylation by SIRT3.

Chemical modifications on histones constitute a key mechanism for gene regulation in chromatin context. Recently, histone lysine β-hydroxybutyrylation (Kbhb) was identified as a new form of histone acylation that connects starvation-responsive metabolism to epigenetic regulation. Sirtuins are a family of NAD-dependent deacetylases.

Interplay between the bacterial protein deacetylase CobB and the second messenger c-di-GMP.

As a ubiquitous bacterial secondary messenger, c-di-GMP plays key regulatory roles in processes such as bacterial motility and transcription regulation. CobB is the Sir2 family protein deacetylase that controls energy metabolism, chemotaxis, and DNA supercoiling in many bacteria. Using an Escherichia coli proteome microarray, we found that c-di-GMP strongly binds to CobB.

Beyond histone acetylation-writing and erasing histone acylations.

Histone post-translational modifications are crucial epigenetic mechanisms regulating a variety of biological events. Besides histone lysine acetylation, a repertoire of acylation types have been identified, including formylation, propionylation, butyrylation, crotonylation, 2-hydroxyisobutyrylation, β-hydroxybutyrylation, succinylation, malonylation, glutarylation and benzoylation. From a structural perspective, here we summarize the writers and erasers of histone acylations and explain the molecular basis of these enzymes catalyzing non-acetyl histone acylations with a focus on histone crotonylation and β-hydroxybutyrylation.

Conserved TCP domain of Sas-4/CPAP is essential for pericentriolar material tethering during centrosome biogenesis.

Pericentriolar material (PCM) recruitment to centrioles forms a key step in centrosome biogenesis. Deregulation of this process leads to centrosome aberrations causing disorders, one of which is autosomal recessive primary microcephaly (MCPH), a neurodevelopmental disorder where brain size is reduced. During PCM recruitment, the conserved centrosomal protein Sas-4/CPAP/MCPH6, known to play a role in centriole formation, acts as a scaffold for cytoplasmic PCM complexes to bind and then tethers them to centrioles to form functional centrosomes.