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Enhancing Robustness of Sortase A by Loop Engineering and Backbone Cyclization
Author(s) -
Zou Zhi,
Mate Diana M.,
Nöth Maximilian,
Jakob Felix,
Schwaneberg Ulrich
Publication year - 2020
Publication title -
chemistry – a european journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.687
H-Index - 242
eISSN - 1521-3765
pISSN - 0947-6539
DOI - 10.1002/chem.202002740
Subject(s) - sortase a , bioconjugation , sortase , robustness (evolution) , chemistry , peptide , conjugate , ligation , staphylococcus aureus , amine gas treating , combinatorial chemistry , biophysics , biochemistry , bacterial protein , microbiology and biotechnology , biology , bacteria , organic chemistry , genetics , mathematics , mathematical analysis , gene
Staphylococcus aureus sortase A (SaSrtA) is widely used for site‐specific protein modifications, but it lacks the robustness for performing bioconjugation reactions at elevated temperatures or in presence of denaturing agents. Loop engineering and subsequent head‐to‐tail backbone cyclization of SaSrtA yielded the cyclized variant CyM6 that has a 7.5 °C increased melting temperature and up to 4.6‐fold increased resistance towards denaturants when compared to the parent rM4. CyM6 gained up to 2.6‐fold (vs. parent rM4) yield of conjugate in ligation of peptide and primary amine under denaturing conditions.