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001029094 1001_ $$0P:(DE-Juel1)176380$$aCamargo, Luana Cristina$$b0
001029094 245__ $$aA Snake Venom Peptide and Its Derivatives Prevent Aβ 42 Aggregation and Eliminate Toxic Aβ 42 Aggregates In Vitro
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001029094 520__ $$aOver a century has passed since Alois Alzheimer first described Alzheimer's disease (AD), and since then, researchers have made significant strides in understanding its pathology. One key feature of AD is the presence of amyloid-β (Aβ) peptides, which form amyloid plaques, and therefore, it is a primary target for treatment studies. Naturally occurring peptides have garnered attention for their potential pharmacological benefits, particularly in the central nervous system. In this study, nine peptide derivatives of Crotamine, a polypeptide from Crotalus durissus terrificus Rattlesnake venom, as well as one d-enantiomer, were evaluated for their ability to modulate Aβ42 aggregation through various assays such as ThT, QIAD, SPR, and sFIDA. All tested peptides were able to decrease Aβ42 aggregation and eliminate Aβ42 aggregates. Additionally, all of the peptides showed an affinity for Aβ42. This study is the first to describe the potential of crotamine derivative peptides against Aβ42 aggregation and to identify a promising d-peptide that could be used as an effective pharmacological tool against AD in the future.
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001029094 7001_ $$0P:(DE-Juel1)171922$$aGering, Ian$$b1
001029094 7001_ $$0P:(DE-Juel1)192216$$aMastalipour, Mohammadamin$$b2
001029094 7001_ $$0P:(DE-Juel1)172001$$aKraemer-Schulien, Victoria$$b3
001029094 7001_ $$0P:(DE-Juel1)162212$$aBujnicki, Tuyen$$b4
001029094 7001_ $$0P:(DE-Juel1)132029$$aWillbold, Dieter$$b5
001029094 7001_ $$0P:(DE-Juel1)180738$$aCoronado, Mônika A.$$b6
001029094 7001_ $$0P:(DE-Juel1)179561$$aEberle, Raphael J.$$b7$$eCorresponding author
001029094 773__ $$0PERI:(DE-600)2528493-9$$a10.1021/acschemneuro.4c00089$$gVol. 15, no. 14, p. 2600 - 2611$$n14$$p2600 - 2611$$tACS chemical neuroscience$$v15$$x1948-7193$$y2024
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