Enzyme-Mediated Site-Specific Antibody−Protein Modification Using a ZZ Domain as a Linker

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• 作者：Takayuki Sakamoto ; Shiori Sawamoto ; Tsutomu Tanaka ; Hideki Fukuda ; Akihiko Kondo
• 刊名：Bioconjugate Chemistry
• 出版年：2010
• 出版时间：December 15, 2010
• 年：2010
• 卷：21
• 期：12
• 页码：2227-2233
• 全文大小：282K
• 年卷期：v.21,no.12(December 15, 2010)
• ISSN：1520-4812

文摘

A ZZ domain (ZZ) and alkaline phosphatase (AP), luciferase (Luc), or glucose oxidase (GOD) were conjugated using Sortase A (SrtA) from Staphylococcus aureus. The specific peptidyl linker for SrtA was genetically fused to the C-terminus of ZZ, and the other linker was fused to the N-terminus of AP, Luc, or GOD, respectively. The resultant proteins were obtained separately by bacterial expression. The recombinant peptide-tagged ZZ and AP, Luc, or GOD were site-specifically conjugated by SrtA through the extra peptidyl linkers in vitro. The SrtA reaction had little influence on either the antibody-binding activity of the ZZ moiety or the enzymatic activity of AP, Luc, or GOD moieties of the conjugates. Additionally, antibody-ZZ-proteins were yielded easily by mixing antibody with ZZ-AP, ZZ-Luc, or ZZ-GOD, allowing their use in an enzyme-linked immunosorbent assay. These results suggest that the enzymatic approach with SrtA facilitates the construction of ZZ-proteins. Furthermore, mixing antibody and ZZ-proteins produces a wide variety of antibody-ZZ-proteins.