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Fujikawa, R.

Publications and source records attributed to Fujikawa, R..

2 recordsLinked to original sources

Cell Morphology and Biophysical Mechanisms-Informed Traction Force Microscopy Using Machine Learning

AO_SCPLOWBSTRACTC_SCPLOWQuantitative evaluation of cell motility is essential for understanding biological functions. Traction force microscopy (TFM) is a method for quantifying cellular traction forces. By performing inverse mathematical analysis of substrate deformations induced by cellular forces, it is possible to estimate the underlying traction forces. Among various approaches for detecting substrate deformations, the most widely used is to track the displacement of fluorescent beads randomly embedded in the substrate. However, it is well known that the accuracy of force estimation deteriorates when the observation density is low. Furthermore, standardized datasets have not been established, as validation settings--such as random force distributions on the substrate, cell size, and bead density--vary across studies. To enable quantitative evaluation, we constructed a dataset based on the biophysical mechanism by which cellular traction forces are transmitted to the substrate through stress fibers, clutch proteins, and focal adhesions. In addition, we proposed a novel machine learning model that incorporates cell shape information obtained from observations, and we designed a loss function that accounts for both force magnitude and direction. As a result, our method enables highly accurate force estimation even under sparse observation conditions.

biophysics↗

Effect of translation enhancing nascent SKIK peptide on the arrest peptides containing consecutive Proline

Ribosome arrest peptides (RAPs) such as SecM arrest peptide (SecM AP) and WPPP with consecutive Pro residues, are known to induce translational stalling in Escherichia coli. We demonstrate that the translation enhancing SKIK peptide tag, which consisted of four amino acid residues Ser-Lys-Ile-Lys, effectively alleviate translational arrest caused by WPPP. Moreover, the proximity between SKIK and WPPP significantly influences the extent of this alleviation, observed in both PURE cell-free protein synthesis and in vivo protein production systems, resulting in a substantial increase in the yield of proteins containing such RAPs. Furthermore, we unveil that nascent SKIK peptide tag and translation elongation factor P (EF-P) which alleviate ribosome stalling in consecutive-Pro rich protein, synergistically promote translation. A kinetic analysis based on the generation of super folder green fluorescent protein under in vitro translation reaction reveals that the ribosome turnover is enhanced by more than 10-fold when the SKIK peptide tag is positioned immediately upstream of the SecM AP sequence. Our findings provide valuable insights into optimizing protein production processes, which are essential for advancing synthetic biology applications. O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=98 SRC="FIGDIR/small/582505v2_ufig1.gif" ALT="Figure 1"> View larger version (13K): org.highwire.dtl.DTLVardef@c97150org.highwire.dtl.DTLVardef@12e3fb1org.highwire.dtl.DTLVardef@157af4forg.highwire.dtl.DTLVardef@1b67da9_HPS_FORMAT_FIGEXP M_FIG C_FIG

synthetic biology↗