http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2015033392-A

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_8e071d18fea054bf8d1420d483e78ed1
classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y02P20-52
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07K14-435
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filingDate 2014-11-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_590cc443536a933d9b471ea980a4a6ac
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f70cab12af0104a782865afefe43b13a
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_79f7bf74558f33e0237dd5e0ee62184a
publicationDate 2015-02-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-2015033392-A
titleOfInvention Protein surface remodeling
abstract A system for routine modification is provided to make proteins more stable and / or to prevent aggregation. Aggregation is a major cause of poor protein behavior. Systems are provided for modifying proteins to produce more stable variants. The method involves identifying non-conserved hydrophobic amino acid residues on the protein surface that are suitable for mutating to more hydrophilic residues (eg, charged amino acids). Any number of residues on the surface are modified to produce variants that are more soluble, have a higher resistance to aggregation, have a higher refolding ability, and / or are more stable in various conditions There is a case. The present invention also provides GFP, streptavidin, and GST variants with high theoretical net charge produced by the techniques of the present invention. Also provided are kits for performing such modifications in any protein of interest. [Selection] Figure 1
priorityDate 2006-06-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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