Publications by authors named "Atlal El-Assaad"

Article Synopsis
  • SARS-CoV-2, responsible for COVID-19, has numerous global variants, with a focus on mutations in the spike protein (S protein) that aid the virus in binding to host cells.
  • Researchers examined ionic amino acid mutations in the S1 spike protein when interacting with Antibody CC12.1, using a computational model and advanced calculations of binding free energy.
  • The study identified specific mutations that could enhance the virus's ability to resist the antibody, suggesting potential future threats beyond existing variants, with some mutations acting as strong inhibitors and others as mild inhibitors in terms of binding affinity.
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Transcription factors (TFs) play important roles in many biochemical processes. Many human genetic disorders have been associated with mutations in the genes encoding these transcription factors, and so those mutations became targets for medications and drug design. In parallel, since many transcription factors act either as tumor suppressors or oncogenes, their mutations are mostly associated with cancer.

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Degradomics is a novel discipline that involves determination of the proteases/substrate fragmentation profile, called the substrate degradome, and has been recently applied in different disciplines. A major application of degradomics is its utility in the field of biomarkers where the breakdown products (BDPs) of different protease have been investigated. Among the major proteases assessed, calpain and caspase proteases have been associated with the execution phases of the pro-apoptotic and pro-necrotic cell death, generating caspase/calpain-specific cleaved fragments.

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The crucial biological role of proteases has been visible with the development of degradomics discipline involved in the determination of the proteases/substrates resulting in breakdown-products (BDPs) that can be utilized as putative biomarkers associated with different biological-clinical significance. In the field of cancer biology, matrix metalloproteinases (MMPs) have shown to result in MMPs-generated protein BDPs that are indicative of malignant growth in cancer, while in the field of neural injury, calpain-2 and caspase-3 proteases generate BDPs fragments that are indicative of different neural cell death mechanisms in different injury scenarios. Advanced proteomic techniques have shown a remarkable progress in identifying these BDPs experimentally.

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Protein-DNA interaction is of fundamental importance in molecular biology, playing roles in functions as diverse as DNA transcription, DNA structure formation, and DNA repair. Protein-DNA association is also important in medicine; understanding Protein-DNA binding kinetics can assist in identifying disease root causes which can contribute to drug development. In this perspective, this work focuses on the transcription process by the GATA Transcription Factor (TF).

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Article Synopsis
  • Bioinformatics is being used in many areas of medicine, like cancer and neuroscience, to help understand diseases better.
  • In psychiatry, it uses advanced tools to analyze lots of data, which helps researchers learn new things about mental health conditions.
  • One key part of bioinformatics is pathway analysis, which looks at how different biological processes work together and can help find new ways to diagnose and treat diseases.
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The complement system is a component of innate immunity and is activated by a cascade of protein interactions whose function is vital to our ability to fight infection. When proper regulation fails, the complement system is unable to recognize "self" from "nonself" and, therefore, attacks own tissues leading to autoimmune diseases. The central protein of the complement system is C3, which is the convergence point of three independently activated but communicating pathways.

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