4.5 Article

Solution structure of DnaE intein from Nostoc punctiforme: Structural basis for the design of a new split intein suitable for site-specific chemical modification

Journal

FEBS LETTERS
Volume 583, Issue 9, Pages 1451-1456

Publisher

WILEY
DOI: 10.1016/j.febslet.2009.03.058

Keywords

Intein; Protein splicing; NMR spectroscopy; Protein ligation; Nuclear spin relaxation; Chemical modification; Protein trans-splicing

Funding

  1. Academy of Finland [118385]
  2. Centre for International Mobility (CIMO)
  3. Academy of Finland (AKA) [118385, 118385] Funding Source: Academy of Finland (AKA)

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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. (C) 2009 Federation of European Biochemical Societies. Published by Elsevier B. V. All rights reserved.

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