Unfolding Top7 loses secondary structure (x) after tertiary interactions, unlike the one-step unfolding of natural proteins.
BAKER/ELSEVIER
Previous tests relied on proteins that had been modified extensively but were still based on naturally occurring protein structures. These variants also folded rapidly, suggesting that cooperative folding might be intrinsic to any protein of a certain size and final stability.
The Washington group thought, however, that Top7 would make a more rigorous test substrate. They had computationally designed Top7 to be stable despite its completely novel fold and structure. Its folding,...
The Rockefeller University Press
2007
The Rockefeller University Press
2007
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