MBE Australasian Protein Structural Phylogenetics Meeting (APSPM 2026)
Meeting Announcement
Updates every hour. Last Updated: 1-Dec-2025 04:11 ET (1-Dec-2025 09:11 GMT/UTC)
The University of Queensland, Brisbane, Australia will host the first Australasian Protein Structural Phylogenetics Meeting (APSPM 2026), a regional meeting of the Society for Molecular Biology and Evolution (SMBE), on February 15 to 18, 2026.
A joint research team led by Dr. Hee-Eun Song of the Photovoltaics Research Department at the Korea Institute of Energy Research (President Yi Chang-Keun, hereafter “KIER”) and Prof. Ka-Hyun Kim of the Department of Physics at Chungbuk National University (President Koh Chang-Seup, hereafter “CBNU”) has successfully identified, for the first time, the specific types of defects responsible for efficiency loss in silicon heterojunction (SHJ) solar cells. The findings are expected to significantly contribute to improving solar cell efficiency when combined with defect-suppression (passivation) techniques.
An international research team from the Songshan Lake Materials Laboratory (SLAB), the Institute of Physics at the Chinese Academy of Sciences, and the International Iberian Nanotechnology Laboratory have developed a novel lead-doped ruthenium-iridium oxide (RuIrPbOₓ) catalyst that exhibits outstanding stability and efficiency for oxygen evolution reactions (OER) in proton exchange membrane water electrolyzers (PEMWEs) operating at high current densities of 3 A/cm². This work addresses longstanding challenges in catalyst durability and performance under acidic, harsh conditions, paving the way for more reliable and cost-effective hydrogen production technologies.
Professor Xiao Shen's research group at Wuhan University developed a new type of palladium-catalyzed tandem cyclization reaction between trifluoroacetylsilane and 1,3-enyne. This strategy effectively suppressed competitive cyclopropanation and cyclopropenylation pathways, selectively promoting the formation of trifluoromethyl-substituted oxatrienes. Subsequently, oxa-6π-electrocyclization efficiently converted them into a series of 6-CF3-2H-pyran derivatives. The authors elucidated the tandem reaction mechanism through DFT calculations: the carbon-carbon triple bond in the 1,3-enyne substrate preferentially inserts into the Pd-Si bond of the acyl divalent palladium intermediate, followed by reductive elimination to generate trifluoromethyl-substituted oxatriene compounds, and finally undergoes oxa-6π-electrocyclization to release the 6-CF3-2H-pyran product. The article was published as an open access research article in CCS Chemistry, the flagship journal of the Chinese Chemical Society.