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Chalik, M.

Publications and source records attributed to Chalik, M..

2 recordsLinked to original sources

StabilizeIT: An Automated Workflow for Protein Stabilization

The industrial application of enzymes is often hampered by poor stability and low expression yields. While computational tools can predict stabilizing mutations, many are bound by restrictive licenses that hinder their broader adoption. To address this, we developed StabilizeIT, a powerful, open-access webserver for enhancing protein stability and expression. StabilizeIT integrates a pipeline of curated open-source tools such as ProteinMPNN, AlphaFold2 and SaProt with our state-of-the-art model, SolvIT, which accurately predicts heterologous expression titers in E. coli. This unique combination allows for the simultaneous optimization of melting temperature (Tm) and solubility. The pipeline exhibits remarkable speed, generating dozens of high-quality candidates with predicted high titers and increased stability in under an hour, streamlining the path to experimental validation. To demonstrate its efficacy, StabilizeIT was used to engineer multiple enzymes in our novel biosynthetic pathway for Hyaluronic Acid. The resulting variants showed greatly enhanced thermal stability and expression, proving the pipelines real-world utility. StabilizeIT is now available to the community, offering an accessible and validated solution to accelerate the development of robust proteins for diverse applications. The webserver is freely available at https://stabilizeit.enzymit.com

bioinformatics↗

LY6S, a New Interferon-Inducible Human Member of the Ly6a-Subfamily Expressed by Spleen Cells and Associated with Inflammation and Viral Resistance

Syntenic genomic loci on human chromosome 8 (hChr8) and mouse chromosome 15 (mChr15) code for LY6/Ly6 (lymphocyte antigen 6) family proteins. The 23 murine Ly6 family genes include eight genes that are flanked by the murine Ly6e and Ly6l genes and form an Ly6 subgroup referred to here as the Ly6a subfamily gene cluster. Ly6a, also known as Sca1 (Stem Cell Antigen-1) and TAP (T-cell activating protein), is a member of the Ly6a subfamily gene cluster. No LY6 genes have been annotated within the syntenic LY6E to LY6L human locus. We report here on LY6S, a solitary human LY6 gene that is syntenic with the murine Ly6a subfamily gene cluster, and with which it shares a common ancestry. LY6S codes for the interferon-inducible GPI-linked LY6S-iso1 protein that contains only 9 of the 10 consensus LY6 cysteine residues and is most highly expressed in a non-classical cell population. Its expression leads to distinct shifts in patterns of gene expression, particularly of genes coding for inflammatory and immune response proteins, and LY6S-iso1 expressing cells show increased resistance to viral infection. Our findings reveal the presence of a previously un-annotated human interferon-stimulated gene, LY6S, which has a one to eight ortholog relationship with the genes of the Ly6a subfamily gene cluster, is most highly expressed in spleen cells of a non-classical cell-lineage and whose expression induces viral resistance and is associated with an inflammatory phenotype and with the activation of genes that regulate immune responses. One Sentence SummaryLY6S is a newly discovered human interferon-inducible gene associated with inflammation and with resistance to viral replication.

genomics↗