5j7d | pdb_00005j7d
Computationally Designed Thioredoxin dF106
Structural highlights
Publication Abstract from PubMedDespite the development of powerful computational tools, the full-sequence design of proteins still remains a challenging task. To investigate the limits and capabilities of computational tools, we conducted a study of the ability of the program Rosetta to predict sequences that recreate the authentic fold of thioredoxin. Focusing on the influence of conformational details in the template structures, we based our study on 8 experimentally determined template structures and generated 120 designs from each. For experimental evaluation, we chose 6 sequences from each of the 8 templates by objective criteria. The 48 selected sequences were evaluated based on their progressive ability to: (1) produce soluble protein in Escherichia coli, (2) yield stable monomeric protein, and (3) the ability of the stable, soluble proteins to adopt the target fold. Of the 48 designs, we were able to synthesize 32, 20 of which resulted in soluble protein. Of these, only two were sufficiently stable to be purified. An X-ray crystal structure was solved for one of the designs, revealing a close resemblance to the target structure. We found a significant difference between the eight template structures to realize the above three criteria despite their high structural similarity. Thus, in order to improve the success rate of computational full-sequence design methods, we recommend that multiple template structures are used. Furthermore, this study shows that special care should be taken when geometry optimizing a structure prior to computational design when using a method that is based on rigid conformations. Computational redesign of thioredoxin is hypersensitive towards minor conformational changes in the backbone template.,Johansson KE, Johansen NT, Christensen S, Horowitz S, Bardwell JC, Olsen JG, Willemoes M, Lindorff-Larsen K, Ferkinghoff-Borg J, Hamelryck T, Winther JR J Mol Biol. 2016 Sep 19. pii: S0022-2836(16)30378-3. doi:, 10.1016/j.jmb.2016.09.013. PMID:27659562[1] From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine. References
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