Matches in SemOpenAlex for { <https://semopenalex.org/work/W4386019279> ?p ?o ?g. }
- W4386019279 endingPage "15" @default.
- W4386019279 startingPage "1" @default.
- W4386019279 abstract "AbstractAmyloid-β peptide, the predominant proteinaceous component of senile plaques, is responsible for the incidence of Alzheimer's disease (AD), an age-associated neurodegenerative disorder. Specifically, the amyloid-β(1-42) (Aβ1-42) isoform, known for its high toxicity, is the predominant biomarker for the preliminary diagnosis of AD. The aggregation of the Aβ1-42 peptides can be affected by the components of the cellular medium through changing their structures and molecular interactions. In this study, we investigated the effect of sodium dodecyl sulfate (SDS) at much lower concentrations than the critical micelle concentration (CMC) on Aβ1-42 aggregation. For this purpose, we studied mono-, di-, tri- and tetramers of Aβ1-42 peptide in two different concentrations of SDS molecules (10 and 40 molecules) using a 300 ns molecular dynamics simulation for each system. The distance between the center of mass (COM) of Aβ1-42 peptides confirms that an increase in the number of SDS molecules decreases their aggregation probability due to greater interaction with SDS molecules. Besides, the less compactness parameter reveals the reduced aggregation probability of Aβ1-42 peptides. Based on the energetic FEL landscapes, SDS molecules with the concentration closer to the CMC are an effective inhibitory agent to prevent the formation of Aβ1-42 fibrils. Also, the aggregation direction of the peptide pairs can be predicted by determining the direction of the accumulation-deterrent forces.Communicated by Ramaswamy H. SarmaKeywords: Alzheimer's diseasesodium dodecyl sulfateamyloid betaMD simulationcritical micelle concentration Disclosure statementNo potential conflict of interest was reported by the authors.Additional informationFundingThe author(s) reported there is no funding associated with the work featured in this article." @default.
- W4386019279 created "2023-08-22" @default.
- W4386019279 creator A5000664644 @default.
- W4386019279 creator A5003496440 @default.
- W4386019279 creator A5061106781 @default.
- W4386019279 creator A5073549005 @default.
- W4386019279 creator A5044972732 @default.
- W4386019279 date "2023-08-20" @default.
- W4386019279 modified "2023-10-09" @default.
- W4386019279 title "Reducing the assemblies of amyloid-beta multimers by sodium dodecyl sulfate surfactant at concentrations lower than critical micelle concentration: molecular dynamics simulation exploration" @default.
- W4386019279 cites W1031578623 @default.
- W4386019279 cites W1482247849 @default.
- W4386019279 cites W1967629642 @default.
- W4386019279 cites W1968587146 @default.
- W4386019279 cites W1975743417 @default.
- W4386019279 cites W1976499671 @default.
- W4386019279 cites W1980624490 @default.
- W4386019279 cites W1985063947 @default.
- W4386019279 cites W1990534979 @default.
- W4386019279 cites W2001391027 @default.
- W4386019279 cites W2005626048 @default.
- W4386019279 cites W2007943717 @default.
- W4386019279 cites W2016251531 @default.
- W4386019279 cites W2017779103 @default.
- W4386019279 cites W2022487013 @default.
- W4386019279 cites W2022772618 @default.
- W4386019279 cites W2023152464 @default.
- W4386019279 cites W2028474034 @default.
- W4386019279 cites W2045725844 @default.
- W4386019279 cites W2050903082 @default.
- W4386019279 cites W2057089150 @default.
- W4386019279 cites W2057477511 @default.
- W4386019279 cites W2063654429 @default.
- W4386019279 cites W2067174909 @default.
- W4386019279 cites W2070104051 @default.
- W4386019279 cites W2076063919 @default.
- W4386019279 cites W2080225612 @default.
- W4386019279 cites W2080684775 @default.
- W4386019279 cites W2081693079 @default.
- W4386019279 cites W2087947478 @default.
- W4386019279 cites W2100610977 @default.
- W4386019279 cites W2105782865 @default.
- W4386019279 cites W2135655560 @default.
- W4386019279 cites W2145170797 @default.
- W4386019279 cites W2157970694 @default.
- W4386019279 cites W2299324286 @default.
- W4386019279 cites W2325791387 @default.
- W4386019279 cites W2329383394 @default.
- W4386019279 cites W2346309772 @default.
- W4386019279 cites W2403327482 @default.
- W4386019279 cites W2528045957 @default.
- W4386019279 cites W2568864464 @default.
- W4386019279 cites W2569256781 @default.
- W4386019279 cites W2614836524 @default.
- W4386019279 cites W2742753529 @default.
- W4386019279 cites W2768767582 @default.
- W4386019279 cites W2800412985 @default.
- W4386019279 cites W2897134950 @default.
- W4386019279 cites W2902588847 @default.
- W4386019279 cites W2904745014 @default.
- W4386019279 cites W2907093370 @default.
- W4386019279 cites W2911230186 @default.
- W4386019279 cites W2931124841 @default.
- W4386019279 cites W2948078675 @default.
- W4386019279 cites W2995037337 @default.
- W4386019279 cites W2996853927 @default.
- W4386019279 cites W3005944381 @default.
- W4386019279 cites W3016377665 @default.
- W4386019279 cites W3030462706 @default.
- W4386019279 cites W3032758350 @default.
- W4386019279 cites W3034480015 @default.
- W4386019279 cites W3081791850 @default.
- W4386019279 cites W3084340297 @default.
- W4386019279 cites W3096606141 @default.
- W4386019279 cites W3159177617 @default.
- W4386019279 cites W3200409661 @default.
- W4386019279 cites W3206837280 @default.
- W4386019279 cites W4205462480 @default.
- W4386019279 cites W4211258827 @default.
- W4386019279 cites W4226272827 @default.
- W4386019279 cites W4280495349 @default.
- W4386019279 cites W4313545390 @default.
- W4386019279 doi "https://doi.org/10.1080/07391102.2023.2247086" @default.
- W4386019279 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/37599504" @default.
- W4386019279 hasPublicationYear "2023" @default.
- W4386019279 type Work @default.
- W4386019279 citedByCount "0" @default.
- W4386019279 crossrefType "journal-article" @default.
- W4386019279 hasAuthorship W4386019279A5000664644 @default.
- W4386019279 hasAuthorship W4386019279A5003496440 @default.
- W4386019279 hasAuthorship W4386019279A5044972732 @default.
- W4386019279 hasAuthorship W4386019279A5061106781 @default.
- W4386019279 hasAuthorship W4386019279A5073549005 @default.
- W4386019279 hasConcept C11268172 @default.
- W4386019279 hasConcept C12554922 @default.
- W4386019279 hasConcept C147597530 @default.
- W4386019279 hasConcept C178790620 @default.
- W4386019279 hasConcept C184651966 @default.