The impact of media, plants and their interactions on bioretention performance: A review.

Bioretention systems have gained considerable popularity as a more natural approach to stormwater management in urban environments. The choice of bioretention media is frequently cited as one of the critical design parameters with the ultimate impact on the performance of the system. The goal of this review is to highlight data that challenge the importance of media as being the dominant design parameter and argue that the long-term performance is shaped by the interactions between media and the living components of a bioretention system, especially vegetation. Some of the key interactions are related to the impact of plant roots on media pore structure, which has implications on infiltration, storage capacity, and treatment. Another relevant interaction pertains to evapotranspiration and the associated impacts on the water balance and the water quality performance of bioretention systems. The impacts of vegetation on the media are highlighted and actual, as well as potential, impacts of plant-media interactions on bioretention performance are presented.

Solution structures of the SH3 domains from Shank scaffold proteins and their interactions with Cav1.3 calcium channels.

Shank proteins are abundant scaffold proteins in the postsynaptic density (PSD) region of brain synapses. Mutations in Shank proteins are associated with autism, schizophrenia, and Alzheimer's disease. To gain insights into Shank protein interactions at the PSD, we determined the solution structures of the src homology 3 (SH3) domains of all three mammalian Shank proteins. Our findings indicate that they have identical and typical SH3 folding motifs, but unusual target-binding pockets. An investigation into the interaction between the Shank SH3 domains and the proline-rich region of the Cav1.3 calcium channel revealed an atypical interaction in which the highly acidic specificity binding pocket of the SH3 domains binds to a Cav1.3 region containing a cluster of three Arg residues. Our study provides insights into Shank SH3-mediated interactions.