In search of the ideal protein sequence |
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Authors: | Godzik A. |
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Affiliation: | Department of Molecular Biology, The Scripps Research Institute 10666 North Torrey Pines Road, La Jolla, CA 92037, USA |
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Abstract: | The inverse of a folding problem is to find the ideal sequencethat folds into a particular protein structure. This problemhas been addressed using the topology fingerprintbased threadingalgorithm, capable of calculating a score (energy) of an arbitrarysequence-structure pair. At first, the search is conducted byunconstrained minimization of the energy in sequence space.It is shown that using energy as the only design criterion leadsto spurious solutions with incorrect amino acid composition.The problem lies in the general features of the protein energysurface as a function of both structure and sequence. The proposedsolution is to design the sequence by maximizing the differencebetween its energy in the desired structure and in other knownprotein structures. Depending on the size of the database ofstructures to avoid, sequences bearing significantsimilarity to the native sequence of the target protein areobtained using this procedure. |
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Keywords: | algorithm/ protein folding/ protein sequence/ structure |
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