Designing Repeat Proteins: Well-expressed, Soluble and Stable Proteins from Combinatorial Libraries of Consensus Ankyrin Repeat Proteins

• Published in: Journal of molecular biology Vol. 332; no. 2; pp. 489 - 503
• Main Authors: Binz, H.Kaspar, Stumpp, Michael T, Forrer, Patrik, Amstutz, Patrick, Plückthun, Andreas
• Format: Journal Article
• Language: English
• Published: England Elsevier Ltd 12.09.2003
• Subjects: Amino Acid Sequence; Ankyrin Repeat; Base Sequence; Circular Dichroism; combinatorial library; Consensus Sequence; Databases, Protein; Escherichia coli; Gene Library; Models, Molecular; Molecular Sequence Data; protein design; Protein Engineering; Protein Structure, Tertiary; Repetitive Sequences, Amino Acid; scaffold; Temperature; PDB, Protein Data Bank; scaffold; ankyrin repeat; consensus sequence; AR, ankyrin repeat; protein design; IMAC, immobilized metal-ion affinity chromatography; combinatorial library
• ISSN: 0022-2836; 1089-8638
• DOI: 10.1016/S0022-2836(03)00896-9

We describe an efficient way to generate combinatorial libraries of stable, soluble and well-expressed ankyrin repeat (AR) proteins. Using a combination of sequence and structure consensus analyses, we designed a 33 amino acid residue AR module with seven randomized positions having a theoretical diversity of 7.2×10 7. Different numbers of this module were cloned between N and C-terminal capping repeats, i.e. ARs designed to shield the hydrophobic core of stacked AR modules. In this manner, combinatorial libraries of designed AR proteins consisting of four to six repeats were generated, thereby potentiating the theoretical diversity. All randomly chosen library members were expressed in soluble form in the cytoplasm of Escherichia coli in amounts up to 200 mg per 1 l of shake-flask culture. Virtually pure proteins were obtained in a single purification step. The designed AR proteins are monomeric and display CD spectra identical with those of natural AR proteins. At the same time, our AR proteins are highly thermostable, with T m values ranging from 66 °C to well above 85 °C. Thus, our combinatorial library members possess the properties required for biotechnological applications. Moreover, the favorable biophysical properties and the modularity of the AR fold may account, partly, for the abundance of natural AR proteins.