Please use this identifier to cite or link to this item:
https://biore.bio.bg.ac.rs/handle/123456789/3637
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Milošević, Jelica | en_US |
dc.contributor.author | Petrić, Jovan | en_US |
dc.contributor.author | Jovčić, Branko | en_US |
dc.contributor.author | Janković, Brankica | en_US |
dc.contributor.author | Polović, Natalija | en_US |
dc.date.accessioned | 2020-11-26T15:37:39Z | - |
dc.date.available | 2020-11-26T15:37:39Z | - |
dc.date.issued | 2020-03 | - |
dc.identifier.issn | 1386-1425 | - |
dc.identifier.uri | https://biore.bio.bg.ac.rs/handle/123456789/3637 | - |
dc.description.abstract | Amyloid fibrils are highly ordered self-assembled (poly)peptide aggregates with cross-β structural pattern. Ovalbumin was used as a model for exploring the potential of infrared spectroscopy in detecting structural transitions and quantitative monitoring of amyloid fibrillation. Low pH (pH 2) and high temperature (90 °C) over the course of 24 h were conditions applied for amyloid formation. Fibrillation of ovalbumin was monitored by ThT and ANS fluorescence, and SDS PAGE. A significant increase in ThT fluorescence with a plateau reached after 4 h of incubation, without the lag phase, was detected. Structural transitions leading to amyloid fibrillation were analysed using all three Amide regions in ATR-FTIR spectra. Significant changes were detected in Amide I and Amide III region (decrease of α-helix and increase of β-sheet peaks). To establish a fast, precise and simple method for quantitative monitoring of amyloid fibrillation, the Amide I/Amide II ratios of aggregation specific β-sheets (1625 and 1695 cm−1, respectively) with 1540 cm−1 as internal standard were used, resulting in good correlation (R2 = 0.93 and 0.95) with the data observed by monitoring ThT fluorescence. On the other hand, assessing aggregation specific β-sheet contents by self-deconvolution showed lower correlation with ThT fluorescence (R2 = 0.75 and 0.64). Here we examined structural transitions during ovalbumin fibrillation in a qualitative and quantitative manner by exploiting the full potential of Amide regions simultaneously. Secondary structure distribution was monitored using second derivative spectra in Amide I region. A novel, simple mathematical calculation for quantitative monitoring of fibrils formation was presented employing that the increase in low and high frequency aggregation specific β-sheet in Amide I region compared to the internal standard in Amide II region is suitable for fibril formation monitoring. | en_US |
dc.relation.ispartof | Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy | en_US |
dc.relation.ispartofseries | 229;11782 | - |
dc.subject | Ovalbumin | en_US |
dc.subject | Amyloid fibrils | en_US |
dc.subject | ATR-FTIR | en_US |
dc.subject | Secondary structures | en_US |
dc.subject | Amide I/AmideIIratio | en_US |
dc.title | Exploring the potential of infrared spectroscopy in qualitative and quantitative monitoring of ovalbumin amyloid fibrillation | en_US |
dc.type | Article | en_US |
dc.identifier.doi | 10.1016/j.saa.2019.117882 | - |
dc.description.rank | M21 | - |
dc.description.impact | 4.098 | - |
item.cerifentitytype | Publications | - |
item.openairetype | Article | - |
item.fulltext | No Fulltext | - |
item.grantfulltext | none | - |
item.openairecristype | http://purl.org/coar/resource_type/c_18cf | - |
crisitem.author.dept | Chair of Biochemistry and Molecular Biology | - |
crisitem.author.orcid | 0000-0002-9500-3786 | - |
Appears in Collections: | Journal Article |
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