Solubility of Aβ40 peptide
(2021) In JCIS Open 4.- Abstract
In this work we measured, by using a direct approach, the equilibrium solubility of recombinant Aβ40 peptide to be S = 0.36 ± 0.15 μM in aqueous solution of 20 mM sodium phosphate buffer at pH 7.4. Microfluidic diffusional sizing (MDS) and mass spectrometry (MALDI-TOF/TOF) with isotope standard were used to quantify the concentration of soluble Aβ40 species coexisting with formed fibrils. A sample set of Aβ40 at different concentrations was incubated at 37 °C under quiescent conditions and for different incubation times. After incubation, the samples were centrifuged and the concentration of Aβ40 in the supernatant was determined. This allowed us to also determine the metastable zone in supersaturated Aβ40 monomer solutions, as a... (More)
In this work we measured, by using a direct approach, the equilibrium solubility of recombinant Aβ40 peptide to be S = 0.36 ± 0.15 μM in aqueous solution of 20 mM sodium phosphate buffer at pH 7.4. Microfluidic diffusional sizing (MDS) and mass spectrometry (MALDI-TOF/TOF) with isotope standard were used to quantify the concentration of soluble Aβ40 species coexisting with formed fibrils. A sample set of Aβ40 at different concentrations was incubated at 37 °C under quiescent conditions and for different incubation times. After incubation, the samples were centrifuged and the concentration of Aβ40 in the supernatant was determined. This allowed us to also determine the metastable zone in supersaturated Aβ40 monomer solutions, as a function of the observation time, as well as the monomer concentration coexisting with formed fibrils. Moreover, the hydrodynamic radius (RH) of the Aβ40 species detected in the supernatant at different time points was also measured, and showed a constant value of ∼1.8 nm, consistent with random coil Aβ40 monomers.
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- author
- Lattanzi, Veronica LU ; Bernfur, Katja LU ; Sparr, Emma LU ; Olsson, Ulf LU and Linse, Sara LU
- organization
- publishing date
- 2021
- type
- Contribution to journal
- publication status
- published
- subject
- keywords
- Alzheimer, Mass spectrometry, Metastable regime, Microfluidics diffusion sizing, Recombinant amyloid beta 40, Solubility
- in
- JCIS Open
- volume
- 4
- article number
- 100024
- publisher
- Elsevier
- external identifiers
-
- scopus:85126581106
- DOI
- 10.1016/j.jciso.2021.100024
- language
- English
- LU publication?
- yes
- id
- 3191eabf-8b70-4bf7-bf90-a3742265923f
- date added to LUP
- 2022-05-02 15:50:01
- date last changed
- 2023-11-21 04:27:14
@article{3191eabf-8b70-4bf7-bf90-a3742265923f, abstract = {{<p>In this work we measured, by using a direct approach, the equilibrium solubility of recombinant Aβ40 peptide to be S = 0.36 ± 0.15 μM in aqueous solution of 20 mM sodium phosphate buffer at pH 7.4. Microfluidic diffusional sizing (MDS) and mass spectrometry (MALDI-TOF/TOF) with isotope standard were used to quantify the concentration of soluble Aβ40 species coexisting with formed fibrils. A sample set of Aβ40 at different concentrations was incubated at 37 °C under quiescent conditions and for different incubation times. After incubation, the samples were centrifuged and the concentration of Aβ40 in the supernatant was determined. This allowed us to also determine the metastable zone in supersaturated Aβ40 monomer solutions, as a function of the observation time, as well as the monomer concentration coexisting with formed fibrils. Moreover, the hydrodynamic radius (R<sub>H</sub>) of the Aβ40 species detected in the supernatant at different time points was also measured, and showed a constant value of ∼1.8 nm, consistent with random coil Aβ40 monomers.</p>}}, author = {{Lattanzi, Veronica and Bernfur, Katja and Sparr, Emma and Olsson, Ulf and Linse, Sara}}, keywords = {{Alzheimer; Mass spectrometry; Metastable regime; Microfluidics diffusion sizing; Recombinant amyloid beta 40; Solubility}}, language = {{eng}}, publisher = {{Elsevier}}, series = {{JCIS Open}}, title = {{Solubility of Aβ40 peptide}}, url = {{http://dx.doi.org/10.1016/j.jciso.2021.100024}}, doi = {{10.1016/j.jciso.2021.100024}}, volume = {{4}}, year = {{2021}}, }