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Ontologies are critical for organizing and interpreting complex domain-specific knowledge, with applications in data integration, functional prediction, and knowledge discovery. As the manual curation of ontology annotations becomes increasingly infeasible due to the exponential growth of biomedical and genomic data, natural language processing (NLP)-based systems have emerged as scalable alternatives. Evaluating these systems requires robust semantic similarity metrics that account for hierarchical and partially correct relationships often present in ontology annotations. This study explores the integration of graph-based and language-based embeddings to enhance the performance of semantic similarity metrics. Combining embeddings generated via Node2Vec and large language models (LLMs) with traditional semantic similarity metrics, we demonstrate that hybrid approaches effectively capture both structural and semantic relationships within ontologies. Our results show that combined similarity metrics outperform individual metrics, achieving high accuracy in distinguishing child–parent pairs from random pairs. This work underscores the importance of robust semantic similarity metrics for evaluating and optimizing NLP-based ontology annotation systems. Future research should explore the real-time integration of these metrics and advanced neural architectures to further enhance scalability and accuracy, advancing ontology-driven analyses in biomedical research and beyond. 

The rapid advancements in Artificial Intelligence (AI) hold the promise of transformative benefits across industries, including construction. To navigate this changing landscape, construction students must not only harness AI's potential but also grasp its ethical considerations and potential challenges. As such, there is a growing imperative within construction education to foster AI literacy among prospective professionals. This study developed and integrated an AI in Construction course module into an undergraduate construction management course. The primary goal is to equip students with AI literacy, achieved through a comprehensive approach that encompasses both theoretical knowledge, covering essential AI concepts and their applications in construction, and practical hands-on experiences, exemplified by a project focused on computer vision for personal protective equipment (PPE) inspection. Results from the course module implementation show that students gained a basic understanding of AI fundamentals after the module, such as dataset annotation, model development, deployment, and evaluation. Qualitative feedback indicates students were motivated to explore further AI-related topics in construction, and several topics that are of their interest were identified. These findings affirm the effectiveness of the proposed module and offer valuable insights for further development and enhancement of AI-related modules in construction education. 

Abstract Presenilin-1 (PS1) is the catalytic subunit of γ-secretase which cleaves within the transmembrane domain of over 150 peptide substrates. Dominant missense mutations in PS1 cause early-onset familial Alzheimer’s disease (FAD); however, the exact pathogenic mechanism remains unknown. Here we combined Gaussian accelerated molecular dynamics (GaMD) simulations and biochemical experiments to determine the effects of six representative PS1 FAD mutations (P117L, I143T, L166P, G384A, L435F, and L286V) on the enzyme-substrate interactions between γ-secretase and amyloid precursor protein (APP). Biochemical experiments showed that all six PS1 FAD mutations rendered γ-secretase less active for the endoproteolytic (ε) cleavage of APP. Distinct low-energy conformational states were identified from the free energy profiles of wildtype and PS1 FAD-mutant γ-secretase. The P117L and L286V FAD mutants could still sample the “Active” state for substrate cleavage, but with noticeably reduced conformational space compared with the wildtype. The other mutants hardly visited the “Active” state. The PS1 FAD mutants were found to reduce γ-secretase proteolytic activity by hindering APP residue L49 from proper orientation in the active site and/or disrupting the distance between the catalytic aspartates. Therefore, our findings provide mechanistic insights into how PS1 FAD mutations affect structural dynamics and enzyme-substrate interactions of γ-secretase and APP.