Numerous substrates have been identified for Type I and II arginine methyltransferases (PRMTs). However, the full substrate spectrum of the only type III PRMT, PRMT7, and its connection to type I and II PRMT substrates remains unknown. Here, we use mass spectrometry to reveal features of PRMT7-regulated methylation. We find that PRMT7 predominantly methylates a glycine and arginine motif; multiple PRMT7-regulated arginine methylation sites are close to phosphorylations sites; methylation sites and proximal sequences are vulnerable to cancer mutations; and methylation is enriched in proteins associated with spliceosome and RNA-related pathways. We show that PRMT4/5/7-mediated arginine methylation regulates hnRNPA1 binding to RNA and several alternative splicing events. In breast, colorectal and prostate cancer cells, PRMT4/5/7 are upregulated and associated with high levels of hnRNPA1 arginine methylation and aberrant alternative splicing. Pharmacological inhibition of PRMT4/5/7 suppresses cancer cell growth and their co-inhibition shows synergistic effects, suggesting them as targets for cancer therapy.

Catalysts based on platinum group metals have been a major focus of the chemical industry for decades. We show that plasmonic photocatalysis can transform a thermally unreactive, earth-abundant transition metal into a catalytically active site under illumination. Fe active sites in a Cu-Fe antenna-reactor complex achieve efficiencies very similar to Ru for the photocatalytic decomposition of ammonia under ultrafast pulsed illumination. When illuminated with light-emitting diodes rather than lasers, the photocatalytic efficiencies remain comparable, even when the scale of reaction increases by nearly three orders of magnitude. This result demonstrates the potential for highly efficient, electrically driven production of hydrogen from an ammonia carrier with earth-abundant transition metals.

The shape of a plasmonic nanoparticle strongly controls its light−matter interaction, which in turn affects how specific morphologies may be used in applications such as sensing, photodetection, and active pixel displays. Here, we show that particle shape also controls plasmonic photocatalytic activity. Three different Al nanocrystal morphologies, octopods, nanocubes, and nanocrystals, all with very similar plasmon resonance frequencies, were used as photocatalysts for the H 2 dissociation reaction. We observe widely varying reaction rates for the three different morphologies. Octopods show a 10 times higher reaction rate than nanocrystals and a 5 times higher rate than nanocubes, with lower apparent activation energies than either nanocubes or nanocrystals by 45% and 49%, respectively. A theoretical model of hot electron direct transfer from photoexcited Al nanoparticles to H 2 molecules is consistent with this observed morphological dependence. This research strongly suggests that nanoparticle geometry, in addition to plasmon resonance energy, is a critical factor in plasmonic photocatalyst design.

We characterized the change in photon absorption and scattering properties of plasmonic Au nanoparticles by chemical interface damping.