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filingDate 2009-08-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2014-10-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_632bc6915c2e1c2d206d17f79cc88ab2
publicationDate 2014-10-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-8859730-B2
titleOfInvention Native chemical ligation at serine and threonine sites
abstract A chemoselective chemical ligation method is disclosed. The method joins two peptide segments efficiently to produce a larger peptide or protein, by generating a natural peptide bond (Xaa-Ser and Xaa-Thr) at the ligation site (Xaa represents any 5 amino acid). The method requires two steps (FIG. 1 ( a )): a) reacting the starting peptide(s) to form an acetal intermediate with an acetal group at the ligation site; b) converting said acetal intermediate to a desired peptide or protein with said natural peptide bond.
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