Dataset Information

Toxic Metal Sequestration Exploiting a Unprecedented Low-Molecular-Weight Hydrogel-to-Metallogel Transformation.

ABSTRACT: We report herein the development of a unique low-molecular-weight gelator-induced technique for environmental remediation. The motive of this work is wastewater purification using a gel-based toxic heavy metal sequestration. The essence of this technique was to bring two different functionalities, one capable of multiple coordination and another with gel-forming ability, arranged in tandem within a single ligand molecule. Naturally, the success of the approach depends on whether the two tandem-arrayed functionalities are indeed working in tandem. Our results show that the ligand molecule is an excellent example of concomitant hydrogelator and metallogelator. The most interesting aspects of this study involve the toxic metal sequestration of Pb, Cd, and Hg which was further studied in detail with spectroscopic, microscopic, and diffraction techniques. We also report here a rare property of pure organic hydrogel-to-metallogel transformation which could open up a new avenue on wastewater purification. In essence, the hydrogels can be envisaged as a unique class of metal-free zeolite analogue for environmental remediation not by just absorbance but through absorbance cum coordination, which are further corroborated by the inductively coupled plasma-optical emission spectroscopy results.

SUBMITTER: De A

PROVIDER: S-EPMC6644520 | biostudies-literature | 2018 Jun

REPOSITORIES: biostudies-literature

ACCESS DATA

Publications

Toxic Metal Sequestration Exploiting a Unprecedented Low-Molecular-Weight Hydrogel-to-Metallogel Transformation.

De Avik A Mondal Raju R

ACS omega 20180604 6

We report herein the development of a unique low-molecular-weight gelator-induced technique for environmental remediation. The motive of this work is wastewater purification using a gel-based toxic heavy metal sequestration. The essence of this technique was to bring two different functionalities, one capable of multiple coordination and another with gel-forming ability, arranged in tandem within a single ligand molecule. Naturally, the success of the approach depends on whether the two tandem-a ...[more]

PMID: 31458792

Similar Datasets

Project description:For some neurological disorders, disease is primarily RNA-mediated due to expression of non-coding microsatellite expansion RNAs (RNAexp). Toxicity is thought to result from enhanced binding of proteins to these expansions and depletion from their normal cellular targets. However, experimental evidence for this sequestration model is lacking. Here, we use HITS-CLIP and pre-mRNA processing analysis of human control versus myotonic dystrophy (DM) brains to provide compelling evidence for this RNA toxicity model. MBNL2 binds directly to DM repeat expansions in the brain resulting in depletion from its normal RNA targets with downstream effects on alternative splicing and polyadenylation. Similar RNA processing defects were detected in Mbnl compound knockout mice, highlighted by dysregulation of Mapt splicing and fetal tau isoform expression in adults. These results demonstrate that MBNL proteins are directly sequestered by RNAexp in the DM brain and introduce a powerful experimental tool to evaluate RNA-mediated toxicity in other expansion diseases. HITS-CLIP analysis was performed to identify RNA binding sites of MBNL2 in control, DM type 1 (DM1), and DM type 2 (DM2) autopsy-derived brain (n=3). Two regions of the brain selected for the study included the frontal cortex and hippocampus. Libraries were sequenced and wiggle files were generated for each biological replicate as well as three pooled biological replicates (3BRs) per group (control, DM1, and DM2). In addition, differential CLIP analysis (dCLIP) was performed to normalize binding data between groups and identify statistically significant changes in binding. The dCLIP analysis generated bedgraph files representing normalized binding profiles of MBNL2 in each group (control, DM1, and DM2) for visualization and comparative analysis. PolyA-seq was performed on control, DM1, and DM2 autopsy-derived brain samples (hippocampus and frontal cortex, n=3) as well as wild-type (WT) and Mbnl1; Mbnl2 conditional double knockout (Mbnl1-/-; Mbnl2c/c; Nestin-Cre+/- or DKO) brain (n=3). Libraries were sequenced and the resultant files were processed and aligned to the reference genomes (hg19 and mm10). Further computational processing was performed to remove internal oligo(dT) mis-priming events, identify valid polyA sites, and trim to the exact polyA sites. BedGraph files were generated for each group in human (control, DM1, and DM2) and mouse (WT and Mbnl DKO) for comparative visualization.

Dataset Information

Toxic Metal Sequestration Exploiting a Unprecedented Low-Molecular-Weight Hydrogel-to-Metallogel Transformation.

Publications

Toxic Metal Sequestration Exploiting a Unprecedented Low-Molecular-Weight Hydrogel-to-Metallogel Transformation.

Similar Datasets

OmicsDI is part of the ELIXIR infrastructure