An Orthogonal Fusion Tag for Efficient Protein Purification.

ABDz1 Albumin binding Fusion tag Human serum albumin Orthogonal affinity purification Protein A Protein G

Journal

Methods in molecular biology (Clifton, N.J.)
ISSN: 1940-6029
Titre abrégé: Methods Mol Biol
Pays: United States
ID NLM: 9214969

Informations de publication

Date de publication:
2021
Historique:
entrez: 31 10 2020
pubmed: 1 11 2020
medline: 24 3 2021
Statut: ppublish

Résumé

In this chapter, we present an efficient method for stringent protein purification facilitated by a dual affinity tag referred to as ABDz1, which is based on a 5 kDa albumin-binding domain from Streptococcal Protein G. The small fusion tag enables an orthogonal affinity purification approach based on two successive and highly specific affinity purification steps. This approach is enabled by native binding of ABDz1 to human serum albumin and engineered binding to Staphylococcal Protein A, respectively. The ABDz1-tag can be fused to either terminus of a protein of interest and the purification steps can be carried out using standard laboratory equipment.

Identifiants

pubmed: 33128750
doi: 10.1007/978-1-0716-0775-6_13
doi:

Substances chimiques

Bacterial Proteins 0
IgG Fc-binding protein, Streptococcus 0
Recombinant Fusion Proteins 0
Staphylococcal Protein A 0
Serum Albumin, Human ZIF514RVZR

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

159-166

Auteurs

Johan Nilvebrant (J)

Division of Protein Technology, School of Engineering Sciences in Chemistry, Biotechnology and Health, KTH/AlbaNova University Center, Stockholm, Sweden.

Mikael Åstrand (M)

Division of Protein Technology, School of Engineering Sciences in Chemistry, Biotechnology and Health, KTH/AlbaNova University Center, Stockholm, Sweden.

Sophia Hober (S)

Department of Protein Science, KTH Royal Institute of Technology, School of Engineering Sciences in Chemistry Biotechnology and Health (CBH), AlbaNova University Center, Stockholm, Sweden. sophia@biotech.kth.se.

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