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Inhibitory Effects of Arginine on the Aggregation of Bovine Insulin

Static and dynamic light scattering were used to investigate the effects of L-arginine, commonly used to inhibit protein aggregation, on the initial aggregation kinetics of solutions of bovine insulin in 20% acetic acid and 0.1 M NaCl as a model system for amyloidosis. Measurements were made as a fu...

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Detalles Bibliográficos
Autores principales: Varughese, Michael M., Newman, Jay
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3400368/
https://www.ncbi.nlm.nih.gov/pubmed/22848214
http://dx.doi.org/10.1155/2012/434289
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author Varughese, Michael M.
Newman, Jay
author_facet Varughese, Michael M.
Newman, Jay
author_sort Varughese, Michael M.
collection PubMed
description Static and dynamic light scattering were used to investigate the effects of L-arginine, commonly used to inhibit protein aggregation, on the initial aggregation kinetics of solutions of bovine insulin in 20% acetic acid and 0.1 M NaCl as a model system for amyloidosis. Measurements were made as a function of insulin concentration (0.5–2.0 mM), quench temperature (60–85°C), and arginine concentration (10–500 mM). Aggregation kinetics under all conditions had a lag phase, whose duration decreased with increasing temperature and with increasing insulin concentration but which increased by up to a factor of 8 with increasing added arginine. Further, the initial growth rate after the lag phase also slowed by up to a factor of about 20 in the presence of increasing concentrations of arginine. From the temperature dependence of the lag phase duration, we find that the nucleation activation energy doubles from 17 ± 5 to 36 ± 3 kcal/mol in the presence of 500 mM arginine.
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spelling pubmed-34003682012-07-30 Inhibitory Effects of Arginine on the Aggregation of Bovine Insulin Varughese, Michael M. Newman, Jay J Biophys Research Article Static and dynamic light scattering were used to investigate the effects of L-arginine, commonly used to inhibit protein aggregation, on the initial aggregation kinetics of solutions of bovine insulin in 20% acetic acid and 0.1 M NaCl as a model system for amyloidosis. Measurements were made as a function of insulin concentration (0.5–2.0 mM), quench temperature (60–85°C), and arginine concentration (10–500 mM). Aggregation kinetics under all conditions had a lag phase, whose duration decreased with increasing temperature and with increasing insulin concentration but which increased by up to a factor of 8 with increasing added arginine. Further, the initial growth rate after the lag phase also slowed by up to a factor of about 20 in the presence of increasing concentrations of arginine. From the temperature dependence of the lag phase duration, we find that the nucleation activation energy doubles from 17 ± 5 to 36 ± 3 kcal/mol in the presence of 500 mM arginine. Hindawi Publishing Corporation 2012 2012-07-09 /pmc/articles/PMC3400368/ /pubmed/22848214 http://dx.doi.org/10.1155/2012/434289 Text en Copyright © 2012 M. M. Varughese and J. Newman. https://creativecommons.org/licenses/by/3.0/This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Varughese, Michael M.
Newman, Jay
Inhibitory Effects of Arginine on the Aggregation of Bovine Insulin
title Inhibitory Effects of Arginine on the Aggregation of Bovine Insulin
title_full Inhibitory Effects of Arginine on the Aggregation of Bovine Insulin
title_fullStr Inhibitory Effects of Arginine on the Aggregation of Bovine Insulin
title_full_unstemmed Inhibitory Effects of Arginine on the Aggregation of Bovine Insulin
title_short Inhibitory Effects of Arginine on the Aggregation of Bovine Insulin
title_sort inhibitory effects of arginine on the aggregation of bovine insulin
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3400368/
https://www.ncbi.nlm.nih.gov/pubmed/22848214
http://dx.doi.org/10.1155/2012/434289
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