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Palabras clave – provistas por la editorial

n/a; spider toxin; hybrid immunogen; channel-like pore-forming activity; venom peptides; chemotherapy; piperidine heterocyclic amines; computational docking; insect immune system; venom; toxoplasmosis; wasps; ion channel structure; mechanical allodynia; Dinoponera quadriceps; natural antibiotics; bees; acid-gated currents; nematicide; novel therapeutics; toxins; protons; Hymenoptera venom; ants; chronic pain; heart contractility; transcriptome; drug targets; skin; peptides; LTQ Orbitrap Hybrid Mass Spectrometer; cantharidin; Centruroides limpidus Karch; pilosulin-like peptide; mechanism; scorpion; stent; homology modelling; amphipathic ?-helix structure; Berberomeloe majalis; mass spectrometric analysis; phospholipases D; Nav1.7; biotools; metalloproteases; myrmecology; Tenebrio molitor; antifeedant; ixodicide; virtual screening; Loxosceles; acid-sensing ion channels; small hive beetle; knottins; Nav channel activity; envenomation; pharmacology; Staphylococcus aureus; spider venom; scorpion venom; insecticidal peptide; Formicidae; AMP; de novo sequencing; tertiapin; leishmaniasis; brown spider; proteome; keratitis; Acinetobacter baumannii; neuropathic pain; bee venom; bioinformatics; ICK peptide; human African trypanosomiasis; automated patch-clamp; Hymenoptera; antimicrobial peptide; LyeTxI-b; linear cationic ?-helical peptide; melittin; Chagas disease; mass spectrometry analysis; neutralizing antibodies; apoptosis; protein–peptide interactions; malaria; pH regulation; voltage-gated sodium channel; venom toxicity; insect neurotoxin; solitary wasp; oxaliplatin; arthropod; mastoparan; cold allodynia; pain target; cutaneous disease; pain; NaV; proteomics; industrial biotechnology; ant; directed disulfide bond formation; antivenoms; blister beetle; venom allergens; ICK-like toxins; Loxosceles spp.; alternative treatment; recombinant toxins; FMRF-amide