Search bioRxiv⌕ Search

Biology subjects

Thapa, G.

Publications and source records attributed to Thapa, G..

4 recordsLinked to original sources

Plastic-hydrolytic enzyme classification using explainable deep learning

The rapid accumulation of plastic waste has emerged as a critical environmental threat, driving the need for scalable and effective biodegradation solutions. Hydrolytic plastic-degrading enzymes (PDEs) offer a promising solution, yet their functional classification remains limited by insufficient annotations and enzymatic diversity. In this study, we present an explainable deep learning framework, PEPIC, to classify nine types of PDEs directly from protein sequences. Using a curated dataset of experimentally validated enzymes and an expanded homologous dataset, we built an explainable deep learning model based on convolutional neural networks (PEPIC) for plastic-degrading enzyme prediction. We benchmarked PEPICs performance against state-of-the-art approaches. First, PEPIC demonstrated statistically significant improvements in predictive performance compared to state-of-the-art methods. Second, PEPIC calculates contribution scores for each amino acid in the protein sequence, indicating their influence on the predictions. The model interpretation revealed that regions highlighted by high contribution scores matched conserved catalytic triads and substrate-binding clefts across PET-, PCL-, and PLA-degrading enzymes. Furthermore, structural modeling confirmed the trustworthiness of PEPICs predictions. Finally, PEPIC predicted an uncurated enzyme as a PET-degrading enzyme, which was biologically validated to hydrolyze bis(2-hydroxyethyl) terephthalate (BHET). These findings demonstrate that PEPIC provides accurate and trustworthy predictions of PDEs, facilitating the discovery of novel enzymes and supporting the development of sustainable plastic biodegradation technologies.

bioinformatics↗

Select autosomal dominant DFNA11 deafness mutations activate Myo7A in epithelial cells

Myosin-7A (Myo7A) is a motor protein crucial for the organization and function of stereocilia, specialized actin-rich protrusions on the surface of inner ear hair cells that mediate hearing. Mutations in Myo7A cause several forms of genetic hearing loss, including autosomal dominant DFNA11 deafness. Despite its importance, the structural elements of Myo7A that control its motor activity within cells are not well understood. In this study, we used cultured kidney epithelial cells to screen for mutations that activate the motor-dependent targeting of Myo7A to the tips of apical microvilli on these cells. Our findings reveal that Myo7A is regulated by specific IQ motifs within its lever arm, and that this regulation can function at least partially independent of its tail sequence. Importantly, we demonstrate that many of the DFNA11 deafness mutations reported in patients activate Myo7A targeting, providing a potential explanation for the autosomal dominant genetics of this form of deafness.

cell biology↗

Isoform-specific targeting properties of the protocadherin CDHR5 control its apical delivery to promote brush border assembly

Transporting epithelial cells of the gut and kidney interact with their luminal environment through a densely-packed collection of apical microvilli known as the brush border. Proper brush border assembly depends on the intermicrovillar adhesion complex (IMAC), a protocadherin-based adhesion complex found at the distal tips of microvilli that mediates adhesion between neighboring protrusions to promote their organized packing. Loss of the IMAC adhesion molecule Cadherin-related family member 5 (CDHR5) correlates with poor prognosis of colon cancer patients, though the functional properties of this protocadherin have not been thoroughly explored in relevant cell systems. Here, we show that the two dominant CDHR5 splice isoforms expressed in enterocytes interact to form an apparent cis-oligomer that is competent to target to the apical domain to drive microvillar elongation. The two isoforms exhibited distinct sequence-dependent apical targeting properties, with one isoform requiring its cytoplasmic tail. Library screening identified the Ezrin-associated scaffolds EBP50 and E3KARP as cytoplasmic binding partners for CDHR5. Consistent with this, loss of EBP50 disrupted proper brush border assembly with cells exhibiting markedly reduced apical IMAC levels. Together, our results shed light on the apical targeting determinants of CDHR5 and further define the interactome of the IMAC involved in brush border assembly.

cell biology↗

Smartphone-Operated Affordable PCR Thermal Cycler for the Detection of Antimicrobial Resistant Bacterial Genes

ObjectivesAntimicrobial resistance (AMR) is a global public health threat. Surveillance of AMR requires affordable, rapid, and user-friendly diagnostic method. Our aim was to develop a low-cost thermocycler to perform polymerase chain reaction (PCR). MethodsWe developed a smartphone-operated PCR thermal cycler using locally available recycled materials. The thermal cycler was used for the amplification for three bacterial genes - bla-TEM and bla-CTXM and 16s rRNA in human urine samples. The performance of custom-built thermal cycler was compared with the commercial one. ResultsThe thermal cycler was portable (<1kg weight), required 12 V power supply, 25 {micro}L of solution, and cost only USD50.0. Temperature and time conditions were instructed using a custom-built smartphone application. The ramping rate of was 0.23{degrees}C for heating and 0.43{degrees}C for cooling, set temperatures were within {+/-} 0.5 {degrees}C of target showing a good thermal stability. The antibiotic sensitivity test of human urine samples showed they were highly resistance and multi-resistant. Nearly 46 % (n=54) E. coli isolates were positive in ESBL screening test. The custom-built thermocycler was able to accurately predict the presence of bla-TEM and bla-CTXM genes (n=6). ConclusionsWe developed and demonstrated a portable, low-cost, easy-to-use, and smartphone-operated PCR thermal cycler. Since it is portable, it can be used in remote location and field settings, including places without stable power supply. The use of the thermal cycler system can be extended, beyond the detection of AMR genes, e.g., in clinical diagnosis, genetics, forensic analysis, and environmental protection.

molecular biology↗