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Biology subjects

Haddadi, F.

Publications and source records attributed to Haddadi, F..

3 recordsLinked to original sources

ProtXAI: Explainable AI Reveals Structural Determinants of Protein Dynamics

Molecular dynamics simulations provide atomistic views of protein motions, but conventional analyses often struggle with extracting subtle mechanistic insights from complex trajectories. Here, we present an integrated framework, ProtXAI, combining molecular dynamics and explainable artificial intelligence (XAI), to identify residue-level determinants of conformational change across diverse protein systems. By leveraging inter-residue distance dynamics, deep learning, and sequential relevance propagation, the approach captures both local fluctuations and long-range communication pathways within protein structures. We applied this framework to three mechanistically distinct systems: apolipoprotein E4 (ApoE4), staphylokinase (SAK) variants, and an ancestral luciferase. Across these applications, our XAI-based approach recovered experimentally supported dynamic hotspots: ligand-responsive hinges in ApoE4, mutation-dependent flexibility shifts in SAK, and evolutionary redistribution of motions in the luciferase. ProtXAI also revealed additional long-range couplings not accessible to classical analysis. Together, these findings demonstrate that combining molecular dynamics with XAI provides a general and scalable strategy for dissecting protein dynamics and uncovering structural determinants of function, stability, and evolutionary changes without prior bias. This approach thus advances the current methodological repertoire for analysing proteins and their intrinsic properties. HighlightsMolecular dynamics simulations are increasingly accessible, yet scalable tools for comparative analysis remain limited. We demonstrate that machine learning coupled with explainable AI can automatically extract structural determinants of protein dynamics from trajectories. ProtXAI identifies key dynamic regions across diverse scenarios, including comparison of protein variants, understanding ligand modulation, and single-trajectory analysis. ProtXAI enables scalable, unbiased interpretation of long trajectories, providing an alternative to manual, time-intensive analysis.

bioinformatics↗

Large-scale Annotation of Biochemically Relevant Pockets and Tunnels in Cognate Enzyme-Ligand Complexes

Tunnels in enzymes with buried active sites are key structural features allowing the entry of substrates and the release of products, thus contributing to the catalytic efficiency. Targeting the bottlenecks of protein tunnels is also a powerful protein engineering strategy. However, the identification of functional tunnels in multiple protein structures is a non-trivial task that can only be addressed computationally. We present a pipeline integrating automated structural analysis with an in-house machine-learning predictor for the annotation of protein pockets, followed by the calculation of the energetics of ligand transport via biochemically relevant tunnels. A thorough validation using eight distinct molecular systems revealed that CaverDock analysis of ligand un/binding is on par with time-consuming molecular dynamics simulations, but much faster. The optimized and validated pipeline was applied to annotate more than 17,000 cognate enzyme-ligand complexes. Analysis of ligand un/binding energetics indicates that the top priority tunnel has the most favourable energies in 75 % of cases. Moreover, energy profiles of cognate ligands revealed that a simple geometry analysis can correctly identify tunnel bottlenecks only in 50 % of cases. Our study provides essential information for the interpretation of results from tunnel calculation and energy profiling in mechanistic enzymology and protein engineering. We formulated several simple rules allowing identification of biochemically relevant tunnels based on the binding pockets, tunnel geometry, and ligand transport energy profiles.

bioinformatics↗

In vitro Anti-Cancer Activity of Oliveria decumbens Vent. Extract, an Endemic Persian Medicinal Plant, on HT-29 Colorectal Cancer Cell Line

IntroductionThe top 3 causes of death worldwide include heart disease, injury, and cancer; and cancer records the 2nd place as the leading cause of death in the United States of America after cardiovascular diseases and injuries. Cancer can begin and progress in a very highly twisted and complex pattern and follow the multifactorial route. There is only very few research on medicinal properties Oliveria decumbens rare and valuable plant specially on cancer. So, in this study we tried to cover all needs for future in vivo research. MethodsMTT assay has been performed to estimate the cytotoxicity of the ethanolic extract of the plant. Its free radical capacity evaluation was done by DPPH assay. Furthermore, real-time PCR, the wound-healing assay along with a DNA damage test to study DNA fragmentation characteristics. The plants transcriptomic study was performed by NGS de Novo assembly. ResultOliveria decumbens ethanolic extract showed an Ic50 of 14.39 g/ml. The real-time PCR showed that Oliveria decumbens ethanolic extract significantly induced apoptosis by upregulating the bax gene and slight downregulation of bcl2 an anti-apoptosis gene. The NGS de Novo transcriptome analysis discovered 38 genes responsible for secondary metabolite synthesis so far. The remaining genes and reconstruction of the co-expression network of the transcriptome are underway. ConclusionThe outcome of the Scratch-test and DNA fragmentation confirmed the anti-metastatic and DNA damage properties respectively. Based on these findings; Oliveria decumbens ethanolic extract shall be considered as potential anticancer and chemotherapeutic agents which may elucidate in upcoming studies.

cancer biology↗