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Kishore, V.

Publications and source records attributed to Kishore, V..

3 recordsLinked to original sources

Icecream: High-Fidelity Equivariant Cryo-Electron Tomography

Cryo-electron tomography (cryo-ET) visualizes 3D cellular architecture in near-native states. Recent deep-learning methods (CryoCARE, IsoNet, DeepDeWedge, CryoLithe) improve denoising and artifact correction, but performance remains limited by very low signal-to-noise ratio, a restricted angular range ( missing wedge), and the lack of ground truth. Here, we present Icecream, which follows the broad template of earlier self-supervised approaches, but treats symmetry in a way consistent with the recent equivariant imaging framework (Chen et al., 2021). Coupled with several engineering refinements, including mixed-precision arithmetic, Icecream achieves substantially better denoising and more reliable missing-wedge recovery, while reducing training and inference time relative to comparable baselines. Across diverse experimental datasets, we observe consistent gains in reconstruction quality, both visually and as quantified by Fourier shell correlation (FSC). Our framework extends to any tomography problem that provides two statistically independent reconstructions of the same volume; in cryo-ET these are obtained by dose splitting or angular partitioning of the tilt series.

bioinformatics↗

TICToK: A comprehensive knowledgebase of tattoo ink chemicals and investigation of their associated toxicities and regulations

Tattoos and permanent make-up, involving dermal injection of chemicals, are increasingly popular, with 30-40% of young adults in North America and Europe having at least one tattoo. Recent studies have suggested a possible association between tattooing and health risks, including skin cancers and lymphomas, although no definitive link has yet been established. This study comprehensively catalogs tattoo ink chemicals and investigates their potential adverse effects, addressing the urgent need for greater understanding of tattoo-related health concerns. First, 364 unique tattoo chemicals were identified from various scientific and regulatory sources, with nearly half functioning as pigments. Hazardous chemicals were identified, revealing carcinogens, endocrine disruptors, neurotoxicants, and dermal toxicants. A regulatory analysis based on key EU regulations, including harmonised classifications under Classification, Labelling and Packaging (CLP) regulation, Restriction Entry 75 of the REACH regulation, Cosmetic Products Regulation (CPR), and SVHC candidate list, revealed existing regulatory coverage of tattoo ink chemicals. Curated chemical-disease associations highlighted that some tattoo chemicals are known to cause dermatitis. Further, diverse toxicological information, including experimental results from REACH dossiers, were integrated to construct stressor-AOP network linking 151 chemicals to 362 AOPs, revealing potential carcinogenic mechanisms associated with tattoo ink chemicals. A systems biology approach revealed potential immunomodulatory effects associated with these chemicals. Finally, all findings have been made available through the online database Tattoo Ink Chemicals and associated Toxicities Knowledgebase (TICToK; https://cb.imsc.res.in/tictok), which can support risk assessment and sustainable tattoo practices. Graphical Abstract O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=81 SRC="FIGDIR/small/668261v2_ufig1.gif" ALT="Figure 1"> View larger version (37K): org.highwire.dtl.DTLVardef@6ce8e3org.highwire.dtl.DTLVardef@2dc5aborg.highwire.dtl.DTLVardef@10c67e6org.highwire.dtl.DTLVardef@1795281_HPS_FORMAT_FIGEXP M_FIG C_FIG

pharmacology and toxicology↗

Septum site placement in Mycobacteria - Identification and Characterization of mycobacterial homologues of Escherichia coli MinD

A major virulence trait of Mycobacterium tuberculosis (M. tb) is its ability to enter a dormant state within its human host. Since cell division is intimately linked to metabolic shut down, understanding the mechanism of septum formation and its integration with other events in the division pathway is likely to offer clues to the molecular basis of dormancy. The M. tb genome lacks obvious homologues of several conserved cell division proteins, and this study aimed at identifying and functionally characterising mycobacterial homologues of the E.coli septum site specification protein MinD (Ec MinD). Sequence homology based analyses suggested that the genomes of both M.tb and the saprophyte Mycobacterium smegmatis (M. smegmatis) encode two putative Ec MinD homologues - Rv1708/MSMEG_3743 and Rv3660c/MSMEG_6171. Both Rv1708 and MSMEG_3743 were observed to fully complement the mini-cell phenotype of the E.coli {Delta}minDE mutant HL1, but the other homologues only partially complemented the mutant phenotype. Over-expression of MSMEG_3743 but not MSMEG_6171 in M. smegmatis led to cell elongation and a drastic decrease in CFU counts, indicating the essentiality of MSMEG_3743 in cell-division. Sequence analysis of MSMEG_3743 showed a conserved Walker A motif, the functional role of which was confirmed by a radiolabelled ATPase activity assay. Rv1708 was observed to interact with the chromosome associated proteins ScpA and ParB, pointing to a link between its septum formation role and chromosome segregation. Comparative structural analyses showed Rv1708 to be closer in similarity to Ec MinD than Rv3660c. In summary we have demonstrated that Rv1708 and MSMEG_3743 are true mycobacterial homologues of Ec MinD, adding a critical missing piece to the mycobacterial cell division puzzle.

microbiology↗