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Design of an expression system to enhance MBP-mediated crystallization.
- Source :
-
Scientific reports [Sci Rep] 2017 Jan 23; Vol. 7, pp. 40991. Date of Electronic Publication: 2017 Jan 23. - Publication Year :
- 2017
-
Abstract
- Crystallization chaperones have been used to facilitate the crystallization of challenging proteins. Even though the maltose-binding protein (MBP) is one of the most commonly used crystallization chaperones, the design of optimal expression constructs for crystallization of MBP fusion proteins remains a challenge. To increase the success rate of MBP-facilitated crystallization, a series of expression vectors have been designed with either a short flexible linker or a set of rigid helical linkers. Seven death domain superfamily members were tested for crystallization with this set of vectors, six of which had never been crystallized before. All of the seven targets were crystallized, and their structures were determined using at least one of the vectors. Our successful crystallization of all of the targets demonstrates the validity of our approach and expands the arsenal of the crystallization chaperone toolkit, which may be applicable to crystallization of other difficult protein targets, as well as to other crystallization chaperones.
- Subjects :
- Escherichia coli genetics
Escherichia coli metabolism
Genetic Vectors
Maltose-Binding Proteins biosynthesis
Maltose-Binding Proteins chemistry
Maltose-Binding Proteins genetics
Recombinant Fusion Proteins chemistry
Crystallization methods
Gene Expression
Recombinant Fusion Proteins biosynthesis
Recombinant Fusion Proteins genetics
Subjects
Details
- Language :
- English
- ISSN :
- 2045-2322
- Volume :
- 7
- Database :
- MEDLINE
- Journal :
- Scientific reports
- Publication Type :
- Academic Journal
- Accession number :
- 28112203
- Full Text :
- https://doi.org/10.1038/srep40991