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Methacrylic acid/Tween 80 engineered amorphous calcium phosphate as an effective bioactive reinforcing nanofillers in dental adhesive

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Dental Materials Journal 2025年第2期44卷 190-200页

作者： Maimansomsuk, Siripatsorn Teangrom, Paremai Teanchai, Chayada Sinthuvanich, Chomdao Ruengket, Pakorn Attarataya, Jakrada Akkarachaneeyakorn, Khrongkhwan Department of Chemistry Faculty of Science Kasetsart University Bangkok10900 Thailand Center of Excellence for Innovation in Chemistry Faculty of Science Kasetsart University Bangkok10900 Thailand Research Center Faculty of Dentistry Mahidol University Bangkok10400 Thailand Department of Biochemistry Faculty of Science Kasetsart University Bangkok Thailand Faculty of Science Kasetsart University Bangkok Thailand Genetic Engineering and Bioinformatics Program Graduate School Kasetsart University Bangkok Thailand Nakhon Ratchasima30000 Thailand

Bioactive fillers in dental adhesives are designed to release beneficial ions, such as calcium and phosphate, to help in remineralization process, and preventing secondary caries. Their incorporation also aims to improve the longevity of dental restorations. Herein, CaP nanoparticles were synthesized through a water-in-oil emulsion method using Tween80 as a surfactant and methacrylic acid (MAA). MAA officiated as a co-surfactant and reduced the size of CaP nanoparticle, including improved compatibility with the components of dental adhesive. The incorporation of 2% T80/CaP/MAA nanofillers into dental adhesive demonstrated increased efficiency, as evidenced by a higher degree of conversion (%DC) and greater micro-tensile bond strength (μTBS). More importantly, T80/CaP/ MAA nanofillers were able to induce remineralization process in the dental structure, which was confirmed by EDX mapping and IR imaging. Finally, a cytotoxicity assessment of the dental adhesive containing T80/CaP/MAA showed no significant adverse effects on human fibroblast cells. © 2025, Japanese Society for Dental Materials and Devices. All rights reserved.

关键词： Stem cells

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Identifying reproducible transcription regulator coexpression patterns with single cell transcriptomics

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PLoS Computational Biology 2025年第4期21卷 e1012962页

作者： Morin, Alexander Chu, Ching Pan Pavlidis, Paul Michael Smith Laboratories University of British Columbia VancouverBC Canada Department of Psychiatry University of British Columbia VancouverBC Canada Graduate Program in Bioinformatics University of British Columbia VancouverBC Canada

The proliferation of single cell transcriptomics has potentiated our ability to unveil patterns that reflect dynamic cellular processes such as the regulation of gene transcription. In this study, we leverage a broad collection of single cell RNA-seq data to identify the gene partners whose expression is most coordinated with each human and mouse transcription regulator (TR). We assembled 120 human and 103 mouse scRNA-seq datasets from the literature (>28 million cells), constructing a single cell coexpression network for each. We aimed to understand the consistency of TR coexpression profiles across a broad sampling of biological contexts, rather than examine the preservation of context-specific signals. Our workflow therefore explicitly prioritizes the patterns that are most reproducible across cell types. Towards this goal, we characterize the similarity of each TR’s coexpression within and across species. We create single cell coexpression rankings for each TR, demonstrating that this aggregated information recovers literature curated targets on par with ChIP-seq data. We then combine the coexpression and ChIP-seq information to identify candidate regulatory interactions supported across methods and species. Finally, we highlight interactions for the important neural TR ASCL1 to demonstrate how our compiled information can be adopted for community use. © 2025 Morin et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

关键词： Mammals

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Multi-modal Multitask Learning Model for Simultaneous Classification of Two Epilepsy Biomarkers 27th

Multi-modal Multitask Learning Model for Simultaneous Classi...

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27th International Conference on Pattern Recognition, ICPR 2024

作者： Broti, Nawara Mahmood Sawada, Masaki Takayama, Yutaro Iijima, Keiya Iwasaki, Masaki Ono, Yumie Electrical Engineering Program Graduate School of Science and Technology Meiji University Kanagawa Kawasaki Japan Department of Neurosurgery Yokohama City University Hospital Kanagawa Yokohama Japan Department of Neurosurgery National Center Hospital National Center of Neurology and Psychiatry Tokyo Kodaira Japan Department of Electronics and Bioinformatics School of Science and Technology Meiji University Kanagawa Kawasaki Japan

ISBN: (纸本)9783031781971

Accurate estimation of the epileptogenic zone is critical for surgical treatment of drug-resistant epilepsy. While epilepsy biomarkers detection for epileptogenic zone localization has traditionally relied on expert clinician knowledge, the use of deep learning in this context has recently gained appeal for objective diagnosis and reducing clinician burden. However, previously proposed classifiers for electrocorticogram data focused on only single biomarkers among many types, requiring separate models and large datasets for each. To minimize clinicians’ workload and patients’ sufferings, innovative methods to classify multiple biomarkers using small training datasets and minimal computation time is required. This research marks the first implementation of multi-modal multitask learning in epilepsy biomarker classification, proposing a model to automatically classify two biomarkers—high-frequency oscillations (HFO) and interictal epileptiform discharges (IED)—from separate datasets simultaneously. We validated the proposed model on 1500 annotated HFO and IED candidate signals each, obtained from 5 patients. Our proposed model can perform both HFO and IED classification simultaneously, with cross-validation accuracies of 90.99% and 93.99%;F1 scores were reported as 0.80 and 0.82, respectively. Our leave-one-patient-out experiments achieved 78.03% and 81.19% accuracy for HFO and IED classification, respectively. Compared to existing state-of-the-art classification architectures, our model is shown to be efficient and robust, yet simple and lightweight. The usefulness of sharing parameters between the two classifiers was confirmed in this practical clinical setting of epileptic biomarker detection, potentially contributing to minimizing the number of annotated datasets and realizing robust, accurate, and simultaneous identification of two biomarkers. © The Author(s), under exclusive license to Springer Nature Switzerland AG 2025.

关键词： Deep learning

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Development of a Smartphone-Linked Immunosensing System for Oxytocin Determination

Biosensors

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Biosensors 2025年第4期15卷 261-261页

作者： Sarubo, Miku Suzuki, Yoka Numazaki, Yuka Kudo, Hiroyuki Electrical Engineering Program Graduate School of Science and Technology Meiji University Kanagawa Kawasaki City214-8571 Japan Department of Electronics and Bioinformatics School of Science and Technology Meiji University Kanagawa Kawasaki City214-8571 Japan

We report an optical immunosensing system for oxytocin (OXT) based on image analysis of color reactions in an enzyme-linked immunosorbent assay (ELISA). We employed a miniaturized optical immunosensing unit that was functionally connected to an LED and a smartphone camera. Our system measures OXT levels using a metric called the RGBscore, which is derived from the red, green, and blue (RGB) information in the captured images. By calculating the RGBscore regressively using the brute-force method, this approach can be applied to smartphones with various CMOS image sensors and firmware. The lower detection limit was determined to be 5.26 pg/mL, and the measurement results showed a higher correlation (r = 0.972) with those obtained from conventional ELISA. These results suggest the potential for its application in a simplified health management system for individuals. © 2025 by the authors.

关键词： Firmware

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Genetic variations and clinical significance in young-onset nasopharyngeal cancer: Analysis of EBV interaction with cellular receptor variants and viral glycoproteins

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Heliyon 2025年第1期11卷 e41198页

作者： Dwi Putra, Sulistyo Emantoko Humardani, Farizky Martriano Sulistomo, Hikmawan Wahyu Antonius, Yulanda Jonathan, Jonathan Milyantono, Riyan Charlie Uthary, Artika Ikawaty, Risma Faculty of Biotechnology University of Surabaya Surabaya 60292 Indonesia Magister in Biomedical Science Program Faculty of Medicine Universitas Brawijaya Malang 65112 Indonesia Bioinformatics Research Center Indonesia Bioinformatics and Biomolecular Malang 65162 Indonesia Faculty of Medicine University of Surabaya Surabaya 60292 Indonesia

Nasopharyngeal cancer (NPC), although rare in young individuals worldwide, is significantly influenced by the Epstein-Barr virus (EBV). Considering EBV's widespread prevalence, understanding its role in NPC's future occurrence, disease progression, clinical symptoms, metastatic tendencies, and prognosis is crucial. In this study, we extensively analyzed two young patients with NPC, who displayed distinct clinical features. We utilized Whole Exome Sequencing (WES), concentrating on EBV-interacting receptors, and applied advanced in silico methods for a deeper investigation. These methods included structural analysis via SWISS-MODEL, stability assessments using PremPS, and molecular docking studies with ClusPro. Our focus was to analyze genetic variants identified by WES and confirm EBV presence using RT-qPCR. Our comparative study between the two subjects showed that the first had milder symptoms and a lower metastasis than the second. In the first subject, we identified unique genetic variants: NRP1 c.536T > C (***179Ala) and MYH9 c.4876A > G (***1626Val). Notably, the NRP1 ***179Ala variant caused structural changes leading to protein instability. Molecular docking suggested that this variant enhances interaction more than the wild-type. RT-qPCR validation of EBV showed lower levels in subject one (mutant-NRP1) compared to subject two (wild-type-NRP1). This finding implies that the ***179Ala variant in subject one could obstruct EBV entry, possibly leading to less severe clinical symptoms Our research provides new insights into the genetic factors influencing the clinical presentation of NPC, identifying promising targets for further research and therapeutic interventions. However, additional validation in a larger cohort is required to elucidate the broader impact of these genetic variants. © 2024 The Author(s)

关键词： EBV Genetic variant In-silico Nasopharyngeal cancer NRP1

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Emerging Techniques in Spatial Multiomics: Fundamental Principles and Applications to Dermatology

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Journal of Investigative Dermatology 2025年第5期145卷 1017-1032页

作者： Jia, Bojing B. Sun, Bryan K. Lee, Ernest Y. Ren, Bing Bioinformatics and Systems Biology Graduate Program University of California San Diego La Jolla CA United States Medical Scientist Training Program University of California San Diego La Jolla CA United States Department of Dermatology University of California Irvine Irvine CA United States Department of Dermatology University of California San Francisco San Francisco CA United States Center for Epigenomics Department of Cellular & Molecular Medicine University of California San Diego La Jolla CA United States Institute of Genomic Medicine Moores Cancer Center School of Medicine University of California San Diego La Jolla CA United States

Molecular pathology, such as high-throughput genomic and proteomic profiling, identifies precise disease targets from biopsies but require tissue dissociation, losing valuable histologic and spatial context. Emerging spatial multi-omic technologies now enable multiplexed visualization of genomic, proteomic, and epigenomic targets within a single tissue slice, eliminating the need for labeling multiple adjacent slices. Although early work focused on RNA (spatial transcriptomics), spatial technologies can now concurrently capture DNA, genome accessibility, histone modifications, and proteins with spatially-resolved single-cell resolution. This review outlines the principles, advantages, limitations, and potential for spatial technologies to advance dermatologic research. By jointly profiling multiple molecular channels, spatial multiomics enables novel studies of copy number variations, clonal heterogeneity, and enhancer dysregulation, replete with spatial context, illuminating the skin's complex heterogeneity. © 2024 The Authors

关键词： Dermatopathology Digital pathology Multiomics Multiplexed imaging Spatial sequencing

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Alignment-Free Estimation of Read to Genome Distances and Its Applications

Alignment-Free Estimation of Read to Genome Distances and...

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29th International Conference on Research in Computational Molecular Biology, RECOMB 2025

作者： Şapcı, Ali Osman Berk Mirarab, Siavash Bioinformatics and Systems Biology Graduate Program UC San Diego San DiegoCA92093 United States Department of Electrical and Computer Engineering UC San Diego San DiegoCA92093 United States

ISBN: (纸本)9783031902512

Searching reads from unknown origins in a reference database and finding evolutionarily similar genomes is central to many applications. Quantifying the similarity by estimating the distance between each read and matching references could further help downstream analyses such as taxonomic characterization or even placing the read on a reference phylogeny. Such distances can be computed using alignment. Since alignment becomes impractical for ultra-large reference databases, many use k-mer-based tools for downstream tasks, but these methods do not compute distances. We introduce krepp to compute the distance between a read and a genome using a maximum likelihood framework built around k-mers. We further introduce algorithms to place reads on a reference tree. Empirical evaluations show that krepp accurately estimates distances, scales well with large databases, and can place short reads coming from any part of the genome on a reference phylogeny. © The Author(s), under exclusive license to Springer Nature Switzerland AG 2025.

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Deep learning-based denoising for unbiased analysis of morphology and stiffness in amyloid fibrils

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Computers in Biology and Medicine 2025年 184卷 109410-109410页

作者： Park, Jaehee Cheong, Da Yeon Lee, Gyudo Han, Cheol E. Department of Electronics and Information Engineering Korea University Sejong30019 Korea Republic of Interdisciplinary Graduate Program for Artificial Intelligence Smart Convergence Technology Korea University Sejong30019 Korea Republic of Department of Biotechnology and Bioinformatics Korea University Sejong30019 Korea Republic of

Understanding the morphology of amyloid fibrils is crucial for comprehending the aggregation and degradation mechanisms of abnormal proteins implicated in various diseases, such as Alzheimer's disease, Parkinson's disease, type II diabetes, and various forms of amyloidosis. Atomic force microscopy (AFM) stands as the most representative method for studying amyloid fibril morphology. However, obstacles in AFM images, including noise, salt, and amorphous aggregates, often impede accurate sample quantification. In this study, we developed denoising software employing a U-Net deep learning architecture to address this issue. The software efficiently eliminated various impediments that interfere with fibril analysis in noisy AFM images, thereby facilitating precise quantification of amyloid fibrils. We also developed automated fibril analysis technologies using the denoised AFM images, leading to quicker, more precise, and more objective assessments of fibril morphology. Furthermore, we presented a method for fibril stiffness extraction from a modulus image through mask creation based on a denoised height image. Our approach secures time efficiency and precision in analyzing amyloid morphology, and we believe it will significantly advance the currently stagnant research on amyloid-related diseases. © 2024 The Authors

关键词： Neurodegenerative diseases

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Mapping the Scientific Landscape of Integrated Scheduling Towards Industry 5.0 with A Bibliometric Analysis 6

Mapping the Scientific Landscape of Integrated Scheduling To...

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6th International Conference on Industry 4.0 and Smart Manufacturing, ISM 2024

作者： Putri Ardyanti, Anak Agung Ayu Xie, Zhiqiang Karnyoto, Andrea Stevens Pardamean, Bens Estiyanti, Ni Made School of Computer Science and Technology Harbin University of Science and Technology Harbin150000 China Faculty of Information Technology and Design Primakara University Bali 80226 Indonesia Bioinformatics and Data Science Research Center Bina Nusantara University Jakarta11480 Indonesia Computer Science Department BINUS Graduate Program Master of Computer Science Bina Nusantara University Jakarta 11480 Indonesia School of Management and Business University of Debrecen Debrecen Hungary

The industry is rapidly transitioning from the 4.0 era to the 5.0 era, prompting renewed interest among scholars in scheduling problems. They allow operations to process and assemble various components simultaneously. This bibliometric analysis provides a comprehensive understanding of the diverse research perspectives on the potential challenges of integrated scheduling within the framework. We identified 357 Scopus articles and analysed co-occurrence keyword (CNK) by VOSViewer tools and Global Citation Score (GCS) by Scopus tools. The research data obtained from 1993 to 2023 mainly in the subject areas of Engineering, Computer Science, Maths, and others. CNK identified six cluster keywords, and nine most cited articles based on normalised GCS. These results contribute to our understanding of the development of scheduling algorithms, shifting from an emphasis on manufacturing transfers to contemporary demand-centric research directions. Furthermore, this research provides a valuable perspective for policymakers, plant personnel, and manufacturing managers to make informed decisions. © 2025 The Authors. Published by Elsevier B.V.

关键词： Job shop scheduling

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MV-CLAM: Multi-View Molecular Interpretation with Cross-Modal Projection via Language Model

arXiv

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arXiv 2025年

作者： Ha, Sumin Kim, Jun Hyeong Piao, Yinhua Kim, Sun Interdisciplinary Program in Artificial Intelligence Seoul National University Korea Republic of Bio-MAX/N-Bio Seoul National University Korea Republic of Department of Computer Science and Engineering Seoul National University Korea Republic of Interdisciplinary Program in Bioinformatics Seoul National University Korea Republic of AIGENDRUG Co. Ltd. Korea Republic of

Human expertise in chemistry and biomedicine relies on contextual molecular understanding, a capability that large language models (LLMs) can extend through fine-grained alignment between molecular structures and text. Recent multimodal learning advances focus on cross-modal alignment, but existing molecule-text models ignore complementary information in different molecular views and rely on single-view representations, limiting molecular understanding. Moreover, naïve multi-view alignment strategies face two challenges: (1) separate aligned spaces with inconsistent mappings between molecule and text embeddings, and that (2) existing loss objectives fail to preserve complementary information for fine-grained alignment. This can limit the LLM’s ability to fully understand the molecular properties. To address these issues, we propose MV-CLAM, a novel framework that aligns multi-view molecular representations into a unified textual space using a multi-query transformer (MQ-Former). Our approach ensures cross-view consistency while a token-level contrastive loss preserves diverse molecular features across textual queries. MV-CLAM enhances molecular reasoning, improving retrieval and captioning accuracy. The source code of MV-CLAM is available in https://***/sumin124/***. © 2025, CC BY-NC-SA.

关键词： Molecular docking

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