This chapter describes optimized RNA-seq workflows for studying PNA-CPPs in Escherichia coli and Salmonella enterica; discusses considerations for RNA isolation, sequencing strategies, and data analysis; and emphasizes the importance of robust, reproducible pipelines for reliable data interpretation.
Toby Wilkinson, Jörg Vogel· Methods in molecular biology· 0 citations
This protocol enables effective cell lysis, nucleic acid purification, and efficient removal of genomic DNA while preserving all transcript classes, including small regulatory RNAs (sRNAs), and provides a basis for future studies investigating the gene expression dynamics and regulatory networks of F. nucleatum under d...
Falk Ponath, Jörg Vogel· Methods in molecular biology· 0 citations
SAILR is identified as a central regulator in linking macrophage survival to host-pathogen interaction and disease pathophysiology, and interacts with the antiapoptotic adaptor protein 14-3-3β to support macrophage survival.
A. Westermann, Alexandra Schock, Diyaa Al Din Ashour et al.· Proceedings of the National...· 2 citations
Abstract Neisseria meningitidis is a human-adapted commensal pathogen that must continuously balance nutrient acquisition with stress tolerance. Here, we identify a type II-C CRISPR/Cas-associated small RNA (scaRNA) as a posttranscriptional regulator of the efeUOB operon and oxidative stress responses. Using in vitro R...
Denise Pytlik, Milan Gerovac, Thorsten Bischler et al.· microLife· 0 citations
Findings indicate that the specific identity of the CPP used plays a key role in determining its robustness against the evolution of resistance, and that laboratory evolution can illuminate the remaining gaps in the authors' knowledge on the mechanisms of action of asobiotics.
Adam J. Mulkern, T. Vu, Linda Popella et al.· bioRxiv· 3 citations
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