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Biology subjects

Kil, Y.

Publications and source records attributed to Kil, Y..

3 recordsLinked to original sources

Differential Analysis Reveals Isoform Switching Following Pneumococcal Vaccination

Advances in RNA-sequencing (RNA-seq) technology have enabled scalable and accessible transcriptomics studies. Longitudinal RNA sequencing studies have been used to track gene expression over time, revealing biological pathways and expression patterns. Traditional approaches for such studies rely on pairwise comparisons or linear regression models, but these methods face challenges when dealing with many time points or modeling complex, non-linear expression patterns. Spline regression offers a robust alternative by efficiently capturing temporal patterns. In this study, we apply spline regression to analyze longitudinal RNA-seq data and demonstrate its advantages in isoform-level differential expression analysis. By modeling transcript-level expression, our method captures isoform switching events that can be obscured in traditional gene-level analyses.

bioinformatics↗

Low-cost, scalable, and automated fluid sampling for fluidics applications

We present colosseum, a low-cost, modular, and automated fluid sampling device for scalable fluidic applications. The colosseum fraction collector uses a single motor, can be built for less than $100 using off-the-shelf and 3D-printed components, and can be assembled in less than an hour. Build Instructions and source files are available at https://github.com/pachterlab/colosseum.

bioengineering↗

Thermostability improvement of Aspergillus awamori glucoamylase via directed evolution of its gene located on episomal expression vector in Pichia pastoris

Novel thermostable forms of glucoamylase (GA) from filamentous fungus Aspergillus awamori X100 were constructed using the directed evolution approach based on random mutagenesis by error-prone PCR of the catalytic domain region of glucoamylase gene with its localization on a new episomal expression vector pPEH in Pichia pastoris cells. Of 3000 yeast transformants screened, six new thermostable GA mutants with amino acid substitutions Val301Asp, Thr390Ala, Thr390Ala/Ser436Pro, Leu7Met/His391Tyr, Asp9His/Ile82Phe, Ser8Arg/Gln338Leu were identified and studied. To estimate the effect of every single substitution in the double mutants, we have constructed an appropriate single mutants of GA by site-directed mutagenesis and analyzed their thermal properties. Results of the analysis showed that only Ile82Phe and Ser8Arg mutations caused an increased thermostability. While Leu7Met and Asp9His mutations decreased the thermal stability of GA, and Gln338Leu had little effect, the synergistic effect of double mutant forms Leu7Met/His391Tyr, Asp9His/Ile82Phe and Ser8Arg/Gln338Leu revealed the significant thermostability improvement as compared to wild type GA.

molecular biology↗