TY - JOUR
T1 - Polypeptide synthesis using an expressed peptide as a building block for condensation with a peptide thioester
T2 - Application to the synthesis of phosphorylated p21Max protein(1-101)
AU - Kawakami, Toru
AU - Hasegawa, Koki
AU - Teruya, Kenta
AU - Akaji, Kenichi
AU - Horiuchi, Masataka
AU - Inagaki, Fuyuhiko
AU - Kurihara, Yasuyuki
AU - Uesugi, Seiichi
AU - Aimoto, Saburo
PY - 2001
Y1 - 2001
N2 - An expressed peptide proved to be useful as a building block for the synthesis of a polypeptide via the thioester method. A partially protected peptide segment, for use as a C-terminal building block, could be prepared from a recombinant protein; its N-terminal amino acid residue was transaminated to an α-oxoacyl group, the side-chain amino groups were then protected with t-butoxycarbonyl (Boc) groups, and, finally, the α-oxoacyl group was removed. On the other hand, an O-phosphoserine-containing peptide thioester was synthesized via a solid-phase method using Boc chemistry. These building blocks were then condensed in the presence of silver ions and an active ester component. During the condensation, epimerization at the condensation site could be suppressed by the use of N,N-dimthylformamide (DMF) as a solvent. Using this strategy, a phosphorylated partial peptide of the p21Max protein, [Ser(PO3H2)2,11]-p21Max(1-101), was successfully synthesized.
AB - An expressed peptide proved to be useful as a building block for the synthesis of a polypeptide via the thioester method. A partially protected peptide segment, for use as a C-terminal building block, could be prepared from a recombinant protein; its N-terminal amino acid residue was transaminated to an α-oxoacyl group, the side-chain amino groups were then protected with t-butoxycarbonyl (Boc) groups, and, finally, the α-oxoacyl group was removed. On the other hand, an O-phosphoserine-containing peptide thioester was synthesized via a solid-phase method using Boc chemistry. These building blocks were then condensed in the presence of silver ions and an active ester component. During the condensation, epimerization at the condensation site could be suppressed by the use of N,N-dimthylformamide (DMF) as a solvent. Using this strategy, a phosphorylated partial peptide of the p21Max protein, [Ser(PO3H2)2,11]-p21Max(1-101), was successfully synthesized.
KW - Expressed peptide
KW - Max protein
KW - Peptide building block
KW - Peptide synthesis
KW - Peptide thioester
KW - Phosphorylated peptide
KW - Transamination
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U2 - 10.1002/psc.341
DO - 10.1002/psc.341
M3 - Article
C2 - 11587186
AN - SCOPUS:0034813131
SN - 1075-2617
VL - 7
SP - 474
EP - 487
JO - Journal of Peptide Science
JF - Journal of Peptide Science
IS - 9
ER -