Understanding the self-healing hydrophobic recovery of high-voltage insulators.

Amorphous siloxane polymers are designed to have high dielectric strength for use as high-voltage insulation materials. Surface hydrophobicity is essential and can be impaired by environmental, electrical, or mechanical factors, leading to leakage currents due to dielectric breakdown. Self-recovery is possible and is generally observed over a period of several hours. Using large-scale, all-atom molecular dynamics simulations, the surface wetting of water droplets on the polymer surface is simulated for various surface conditions, including oxidation and coating with small molecules, to understand the driving forces of the recovery process at the atomistic level, which is of primary importance for the developments of novel materials. In this work, we shed light onto the self-recovery mechanism and propose the use of low-molecular-weight (LMW) siloxane to accelerate the recovery of hydrophobicity.

Surface dynamics of amorphous polymers used for high-voltage insulators.

Amorphous siloxane polymers are the backbone of high-voltage insulation materials. The natural hydrophobicity of their surface is a necessary property for avoiding leakage currents and dielectric breakdown. As these surfaces are exposed to the environment, electrical discharges or strong mechanical impact can temporarily destroy their water-repellent properties. After such events, however, a self-healing process sets in and restores the original hydrophobicity within some hours. In the present study, we investigate possible mechanisms of this restoration process. Using large-scale, all-atom molecular dynamics simulations, we show that molecules on the material surface have augmented motion that allows them to rearrange with a net polarization. The overall surface region has a net orientation that contributes to hydrophobicity, and charged groups that are placed at the surface migrate inward, away from the vacuum interface and into the bulk-like region. Our simulations provide insight into the mechanisms for hydrophobic self-recovery that repair material strength and functionality and suggest material compositions for future high-voltage insulators.

Electronic structure of neighboring extein residue modulates intein C-terminal cleavage activity.

Protein splicing is an autocatalytic reaction where an intervening element (intein) is excised and the remaining two flanking sequences (exteins) are joined. The reaction requires specific conserved residues, and activity may be affected by both the intein and the extein sequence. Predicting how sequence will affect activity is a challenging task. Based on first-principles density functional theory and multiscale quantum mechanics/molecular mechanics, we report C-terminal cleavage reaction rates for five mutations at the first residue of the C-extein (+1), and describe molecular properties that may be used as predictors for future mutations. Independently, we report on experimental characterization of the same set of mutations at the +1 residue resulting in a wide range of C-terminal cleavage activities. With some exceptions, there is general agreement between computational rates and experimental cleavage, giving molecular insight into previous claims that the +1 extein residue affects intein catalysis. These data suggest utilization of attenuating +1 mutants for intein-mediated protein manipulations because they facilitate precursor accumulation in vivo for standard purification schemes. A more detailed analysis of the "+1 effect" will also help to predict sequence-defined effects on insertion points of the intein into proteins of interest.

Molecular motion of amorphous silicone polymers.

In this paper, we have studied silicone polymers based on poly(dimethylsiloxane) (PDMS) molecules, which have versatile applications in many fields because of their flexible molecular properties. These polymers are of interest because when used for high-voltage insulation, surfaces exposed to weather need to be hydrophobic because a hydrophilic surface can cause leakage currents. Indeed, after damaging electrical discharges, self-recovery of the hydrophobic surface occurs, requiring molecular diffusion and surface reconstruction for repair. We use large-scale, all-atom molecular dynamics simulations that enable an atomic-level description of molecular motion in mixed, amorphous, PDMS-based materials. The local properties that contribute to enhanced molecular motion are characterized based on their local structural and electrostatic environment. With this knowledge, molecular components with desirable diffusion properties may be designed for improved material functionality.

Spontaneous proton transfer to a conserved intein residue determines on-pathway protein splicing.

The discovery of inteins, which are protein-splicing elements, has stimulated interest for various applications in chemical biology, bioseparations, drug delivery, and sensor development. However, for inteins to effectively contribute to these applications, an increased mechanistic understanding of cleavage and splicing reactions is required. While the multistep chemical reaction that leads to splicing is often explored and utilized, it is not clear how the intein navigates through the reaction space. The sequence of reaction steps must progress in concert in order to yield efficient splicing while minimizing off-pathway cleavage reactions. In this study, we demonstrate that formation of a previously identified branched intermediate is the critical step for determining splicing over cleavage products. By combining experimental assays and quantum mechanical simulations, we identify the electrostatic interactions that are important to the dynamics of the reaction steps. We illustrate, via an animated simulation trajectory, a proton transfer from the first C-terminal extein residue to a conserved aspartate, which synchronizes the multistep enzymatic reaction that is key to splicing. This work provides new insights into the complex interplay between critical active-site residues in the protein splicing mechanism, thereby facilitating biotechnological application while shedding light on multistep enzyme activity.

Highly conserved histidine plays a dual catalytic role in protein splicing: a pKa shift mechanism.

Protein splicing is a precise autocatalytic process in which an intein excises itself from a precursor with the concomitant ligation of the flanking sequences. Protein splicing occurs through acid-base catalysis in which the ionization states of active site residues are crucial to the reaction mechanism. In inteins, several conserved histidines have been shown to play important roles in protein splicing, including the most conserved "B-block" histidine. In this study, we have combined NMR pK(a) determination with quantum mechanics/molecular mechanics (QM/MM) modeling to study engineered inteins from Mycobacterium tuberculosis (Mtu) RecA intein. We demonstrate a dramatic pK(a) shift for the invariant B-block histidine, the most conserved residue among inteins. The B-block histidine has a pK(a) of 7.3 +/- 0.6 in a precursor and a pK(a) of <3.5 in a spliced intein. The pK(a) values and QM/MM data suggest that the B-block histidine has a dual role in the acid-base catalysis of protein splicing. This histidine likely acts as a general base to initiate splicing with an acyl shift and then as a general acid to cause the breakdown of the scissile bond at the N-terminal splicing junction. The proposed pK(a) shift mechanism accounts for the biochemical data supporting the essential role for the B-block histidine and for the near absolute sequence conservation of this residue.