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Affinity precipitation of human serum albumin using a thermo-response polymer with an L-thyroxin ligand

BACKGROUND: Affinity precipitation has been reported as a potential technology for the purification of proteins at the early stage of downstream processing. The technology could be achieved using reversible soluble-insoluble polymers coupled with an affinity ligand to purify proteins from large volu...

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Autores principales: Ding, Zhaoyang, Cao, Xuejun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3903448/
https://www.ncbi.nlm.nih.gov/pubmed/24341315
http://dx.doi.org/10.1186/1472-6750-13-109
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author Ding, Zhaoyang
Cao, Xuejun
author_facet Ding, Zhaoyang
Cao, Xuejun
author_sort Ding, Zhaoyang
collection PubMed
description BACKGROUND: Affinity precipitation has been reported as a potential technology for the purification of proteins at the early stage of downstream processing. The technology could be achieved using reversible soluble-insoluble polymers coupled with an affinity ligand to purify proteins from large volumes of dilute solution material such as fermentation broths or plasma. In this study, a thermo-response polymer was synthesized using N-methylol acrylamide, N-isopropyl acrylamide and butyl acrylate as monomers. The molecular weight of the polymer measured by the viscosity method was 3.06 × 10(4) Da and the lower critical solution temperature (LCST) was 28.0°C.The recovery of the polymer above the LCST was over 95.0%. Human serum albumin (HSA) is the most abundant protein in the human serum system, and it has important functions in the human body. High purity HSA is required in pharmaceuticals. Safe and efficient purification is a crucial process during HSA production. RESULTS: A thermo-response polymer was synthesized and L-thyroxin immobilized on the polymer as an affinity ligand to enable affinity precipitation of HSA. The LCST of the affinity polymer was 31.0°C and the recovery was 99.6% of its original amount after recycling three times. The optimal adsorption condition was 0.02 M Tris–HCl buffer (pH 7.0) and the HSA adsorption capacity was 14.9 mg/g polymer during affinity precipitation. Circular dichroism spectra and a ForteBio Octet system were used to analyze the interactions between the affinity polymer and HSA during adsorption and desorption. The recovery of total HSA by elution with 1.0 mol/L NaSCN was 93.6%. When the affinity polymer was applied to purification of HSA from human serum, HSA could be purified to single-band purity according to SDS-PAGE. CONCLUSION: A thermo-response polymer was synthesized and L-thyroxin was attached to the polymer. Affinity precipitation was used to purify HSA from human serum.
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spelling pubmed-39034482014-02-11 Affinity precipitation of human serum albumin using a thermo-response polymer with an L-thyroxin ligand Ding, Zhaoyang Cao, Xuejun BMC Biotechnol Research Article BACKGROUND: Affinity precipitation has been reported as a potential technology for the purification of proteins at the early stage of downstream processing. The technology could be achieved using reversible soluble-insoluble polymers coupled with an affinity ligand to purify proteins from large volumes of dilute solution material such as fermentation broths or plasma. In this study, a thermo-response polymer was synthesized using N-methylol acrylamide, N-isopropyl acrylamide and butyl acrylate as monomers. The molecular weight of the polymer measured by the viscosity method was 3.06 × 10(4) Da and the lower critical solution temperature (LCST) was 28.0°C.The recovery of the polymer above the LCST was over 95.0%. Human serum albumin (HSA) is the most abundant protein in the human serum system, and it has important functions in the human body. High purity HSA is required in pharmaceuticals. Safe and efficient purification is a crucial process during HSA production. RESULTS: A thermo-response polymer was synthesized and L-thyroxin immobilized on the polymer as an affinity ligand to enable affinity precipitation of HSA. The LCST of the affinity polymer was 31.0°C and the recovery was 99.6% of its original amount after recycling three times. The optimal adsorption condition was 0.02 M Tris–HCl buffer (pH 7.0) and the HSA adsorption capacity was 14.9 mg/g polymer during affinity precipitation. Circular dichroism spectra and a ForteBio Octet system were used to analyze the interactions between the affinity polymer and HSA during adsorption and desorption. The recovery of total HSA by elution with 1.0 mol/L NaSCN was 93.6%. When the affinity polymer was applied to purification of HSA from human serum, HSA could be purified to single-band purity according to SDS-PAGE. CONCLUSION: A thermo-response polymer was synthesized and L-thyroxin was attached to the polymer. Affinity precipitation was used to purify HSA from human serum. BioMed Central 2013-12-17 /pmc/articles/PMC3903448/ /pubmed/24341315 http://dx.doi.org/10.1186/1472-6750-13-109 Text en Copyright © 2013 Ding and Cao; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Ding, Zhaoyang
Cao, Xuejun
Affinity precipitation of human serum albumin using a thermo-response polymer with an L-thyroxin ligand
title Affinity precipitation of human serum albumin using a thermo-response polymer with an L-thyroxin ligand
title_full Affinity precipitation of human serum albumin using a thermo-response polymer with an L-thyroxin ligand
title_fullStr Affinity precipitation of human serum albumin using a thermo-response polymer with an L-thyroxin ligand
title_full_unstemmed Affinity precipitation of human serum albumin using a thermo-response polymer with an L-thyroxin ligand
title_short Affinity precipitation of human serum albumin using a thermo-response polymer with an L-thyroxin ligand
title_sort affinity precipitation of human serum albumin using a thermo-response polymer with an l-thyroxin ligand
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3903448/
https://www.ncbi.nlm.nih.gov/pubmed/24341315
http://dx.doi.org/10.1186/1472-6750-13-109
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