Engineering an ultra-stable affinity reagent based on Top7

• Published in: Protein engineering, design and selection Vol. 22; no. 5; pp. 325 - 332
• Main Authors: Boschek, Curt B., Apiyo, David O., Soares, Thereza A., Engelmann, Heather E., Pefaur, Noah B., Straatsma, Tjerk P., Baird, Cheryl L.
• Format: Journal Article
• Language: English
• Published: England Oxford University Press 01.05.2009; Oxford Publishing Limited (England)
• Subjects: Affinity Labels - chemical synthesis; Affinity Labels - metabolism; Amino Acid Sequence; Carrier Proteins - chemical synthesis; Carrier Proteins - metabolism; CD4 Antigens - metabolism; Chromatography, Gel; Circular Dichroism; Computational Biology - methods; Computer Simulation; engineering affinity; Enzyme-Linked Immunosorbent Assay; Humans; Models, Molecular; molecular dynamics simulations; Mutagenesis; Protein Engineering - methods; protein scaffold; protein stability; Sensitivity and Specificity; Top7; molecular dynamics simulations; protein scaffold; Top7; engineering affinity; protein stability
• ISSN: 1741-0126; 1741-0134
• DOI: 10.1093/protein/gzp007

Antibodies are widely used for diagnostic and therapeutic applications because of their sensitive and specific recognition of a wide range of targets; however, their application is limited by their structural complexity. More demanding applications require greater stability than can be achieved by immunoglobulin-based reagents. Highly stable, protein-based affinity reagents are being investigated for this role with the goal of identifying a suitable scaffold that can attain specificity and sensitivity similar to that of antibodies while performing under conditions where antibodies fail. We have engineered Top7—a highly stable, computationally designed protein—to specifically bind human CD4 by inserting a peptide sequence derived from a CD4-specific antibody. Molecular dynamics simulations were used to evaluate the structural effect of the peptide insertion at a specific site within Top7 and suggest that this Top7 variant retains conformational stability over 100°C. This engineered protein specifically binds CD4 and, consistent with simulations, is extremely resistant to thermal and chemical denaturation—retaining its secondary structure up to at least 95°C and requiring 6 M guanidine to completely unfold. This CD4-specific protein demonstrates the functionality of Top7 as a viable scaffold for use as a general affinity reagent which could serve as a robust and inexpensive alternative to antibodies.