What’s a Spider? Designation of the Neotype for the First Animal Species Ever Described, Araneus angulatus Clerck 1757 (Araneae: Araneidae)

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  What’s a Spider? Designation of the Neotype for the First Animal Species Ever Described, Araneus angulatus Clerck 1757 (Araneae: Araneidae) Abstract We designate a neotype for the Eurasian spider species Araneus angulatus Clerck, 1757, thereby fixing the objective application of the species name, the genus name Araneus Clerck 1757, the family name Araneidae Clerck 1757, and the superfamily name Araneoidea Clerck 1757. By etymology and arachnological tradition, it also unofficially fixes the application of the ordinal name Araneae Clerck 1757 and thus answers the uncontroversial question, “What’s a spider?” A. angulatus also happens to be historically the first animal species ever described because Clerck (1757) has priority over Linnaeus (1758). Neotype designation is justified for three reasons: the syntypes of A. angulatus are lost; “ A. angulatus ” contains significant COI sequence divergence, potentially representing intraspecific variation, misidentifications, or as many...

Potential Role of Tarantula Venom Peptides in Targeting Human Death Receptors: A Computational Study

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Potential Role of Tarantula Venom Peptides in Targeting Human Death Receptors: A Computational Study

Abstract

Animal venom has been gaining traction as a potential source of therapeutics for various diseases. Spiders encompass a wide variety of venom-producing species, of which tarantulas of the family Theraphosidae are widely known across the globe. Research towards tarantula venom therapeutics has led to its potential application as antinociceptives. Death receptors are cellular receptors that induce apoptosis—the body’s natural suicide mechanism—to destroy malfunctioning cells. These are particularly of interest in cancer research, as this mechanism is tampered with, resulting in cancer cell proliferation. In this study, the viability of venom toxins from the Theraphosidae family of spiders to induce apoptosis by binding to human death receptors is investigated by carrying out anti-cancer screening, molecular docking, ADMET evaluation, then molecular dynamics and thermodynamic analysis twice, first to ascertain the best receptor–peptide systems per receptor, and secondly to more comprehensively describe binding stability and thermodynamics. Results point to favorable receptor–peptide interactions due to similarities in equilibrium behavior with the death ligand–death receptor systems, along with favorable end-state binding energies and ADMET analysis results. Further inquiry is recommended to assess the real-life efficacy and viability of theraphotoxins as apoptosis therapeutics and further improve on their ability to induce apoptosis.


Quiambao, J. I., Fowler, P. M., & Tayo, L. L. (2024). Potential Role of Tarantula Venom Peptides in Targeting Human Death Receptors: A Computational Study. Applied Sciences, 14(19), 8701.