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Improved variants of SrtA for site-specific conjugation on antibodies and proteins with high efficiency.
Chen, Long; Cohen, Justin; Song, Xiaoda; Zhao, Aishan; Ye, Zi; Feulner, Christine J; Doonan, Patrick; Somers, Will; Lin, Laura; Chen, Peng R.
Afiliación
  • Chen L; Beijing National Laboratory for Molecular Sciences, College of Chemistry and Molecular Engineering, Synthetic and Functional Biomolecules Center, Peking University, Beijing 100871, China.
  • Cohen J; Department of Global Biotherapeutics Technologies, Pfizer Inc., Cambridge, MA 02140, USA.
  • Song X; School of Life Sciences, Nanjing University, China.
  • Zhao A; Beijing National Laboratory for Molecular Sciences, College of Chemistry and Molecular Engineering, Synthetic and Functional Biomolecules Center, Peking University, Beijing 100871, China.
  • Ye Z; Beijing National Laboratory for Molecular Sciences, College of Chemistry and Molecular Engineering, Synthetic and Functional Biomolecules Center, Peking University, Beijing 100871, China.
  • Feulner CJ; Department of Global Biotherapeutics Technologies, Pfizer Inc., Cambridge, MA 02140, USA.
  • Doonan P; Department of Global Biotherapeutics Technologies, Pfizer Inc., Cambridge, MA 02140, USA.
  • Somers W; Department of Global Biotherapeutics Technologies, Pfizer Inc., Cambridge, MA 02140, USA.
  • Lin L; Department of Global Biotherapeutics Technologies, Pfizer Inc., Cambridge, MA 02140, USA.
  • Chen PR; Beijing National Laboratory for Molecular Sciences, College of Chemistry and Molecular Engineering, Synthetic and Functional Biomolecules Center, Peking University, Beijing 100871, China.
Sci Rep ; 6: 31899, 2016 08 18.
Article en En | MEDLINE | ID: mdl-27534437
ABSTRACT
Sortase mediated ligation is a highly specific platform for conjugation that relies on the specificity of the transpeptidase Sortase A (SrtA) for short peptide sequences (LPXTG and GGG). SrtA retains its specificity while accepting a wide range of potential substrates, but its broad use is limited by the wild-type enzyme's poor kinetics, which require large amounts of SrtA and extended reaction times for efficient conjugation. Prior explorations have aimed to improve the kinetics of SrtA with limited success. Herein we describe the discovery of further improved SrtA variants with increased efficiency for the conjugation reaction, and demonstrate their robustness in labelling proteins and antibodies in a site-specific manner. Our variants require significantly lower amounts of enzyme than WT SrtA and can be used to attach small molecules to the N or C-terminus of the heavy or light chain in antibodies with excellent yields. These improved variants can also be used for highly efficient site-specific PEGylation.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Polietilenglicoles / Coloración y Etiquetado / Proteínas Bacterianas / Cisteína Endopeptidasas / Aminoaciltransferasas / Mutación Missense / Anticuerpos Idioma: En Revista: Sci Rep Año: 2016 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Polietilenglicoles / Coloración y Etiquetado / Proteínas Bacterianas / Cisteína Endopeptidasas / Aminoaciltransferasas / Mutación Missense / Anticuerpos Idioma: En Revista: Sci Rep Año: 2016 Tipo del documento: Article País de afiliación: China
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