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De novo design of a non-local β-sheet protein with high stability and accuracy

E. Marcos, TM. Chidyausiku, AC. McShan, T. Evangelidis, S. Nerli, L. Carter, LG. Nivón, A. Davis, G. Oberdorfer, K. Tripsianes, NG. Sgourakis, D. Baker,

. 2018 ; 25 (11) : 1028-1034. [pub] 20181029

Jazyk angličtina Země Spojené státy americké

Typ dokumentu časopisecké články, Research Support, N.I.H., Extramural, práce podpořená grantem

Perzistentní odkaz   https://www.medvik.cz/link/bmc19034933

Grantová podpora
Howard Hughes Medical Institute - United States
R35 GM125034 National Institute of General Medical Sciences - United States
S10 OD018455 Office of the Director - United States

E-zdroje Online Plný text

NLK ProQuest Central od 2004-01-01 do Před 1 rokem
Health & Medicine (ProQuest) od 2004-01-01 do Před 1 rokem

β-sheet proteins carry out critical functions in biology, and hence are attractive scaffolds for computational protein design. Despite this potential, de novo design of all-β-sheet proteins from first principles lags far behind the design of all-α or mixed-αβ domains owing to their non-local nature and the tendency of exposed β-strand edges to aggregate. Through study of loops connecting unpaired β-strands (β-arches), we have identified a series of structural relationships between loop geometry, side chain directionality and β-strand length that arise from hydrogen bonding and packing constraints on regular β-sheet structures. We use these rules to de novo design jellyroll structures with double-stranded β-helices formed by eight antiparallel β-strands. The nuclear magnetic resonance structure of a hyperthermostable design closely matched the computational model, demonstrating accurate control over the β-sheet structure and loop geometry. Our results open the door to the design of a broad range of non-local β-sheet protein structures.

Citace poskytuje Crossref.org

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