Abstract
Naturally split DnaE intein from Nostoc punctiforme (Npu) has robust protein trans-splicing activity and high tolerance of sequence variations at the splicing junctions. We determined the solution structure of a single chain variant of NpuDnaE intein by NMR spectroscopy. Based on the NMR structure and the backbone dynamics of the single chain NpuDnaE intein, we designed a functional split variant of the NpuDnaE intein having a short C-terminal half (C-intein) composed of six residues. In vivo and in vitro protein ligation of model proteins by the newly designed split intein were demonstrated.
Original language | English |
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Pages (from-to) | 1451-1456 |
Number of pages | 6 |
Journal | FEBS Letters |
Volume | 583 |
Issue number | 9 |
DOIs | |
Publication status | Published - 6 May 2009 |
MoE publication type | A1 Journal article-refereed |
Keywords
- Chemical modification
- Intein
- NMR spectroscopy
- Nuclear spin relaxation
- Protein ligation
- Protein splicing
- Protein trans-splicing