3b83

Publication Abstract from PubMed

The de novo design of globular beta sheet proteins remains largely an unsolved problem. It is unclear whether most designs are failing because the designed sequences do not have favorable energies in the target conformations or whether more emphasis should be placed on negative design, that is, explicitly identifying sequences that have poor energies when adopting undesired conformations. We tested whether we could redesign the sequence of a naturally occurring beta sheet protein, tenascin, with a design algorithm that does not include explicit negative design. Denaturation experiments indicate that the designs are significantly more stable than the wild-type protein and the crystal structure of one design closely matches the design model. These results suggest that extensive negative design is not required to create well-folded beta sandwich proteins. However, it is important to note that negative design elements may be encoded in the conformation of the protein backbone which was preserved from the wild-type protein.

Computer-based redesign of a beta sandwich protein suggests that extensive negative design is not required for de novo beta sheet design.,Hu X, Wang H, Ke H, Kuhlman B Structure. 2008 Dec 10;16(12):1799-805. PMID:19081056^[1]

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.