The extracellular Ig domain I of Emmprin (34-94) carrying a chitobiose unit
at Asn(44) was chemically synthesized. Boc-Asn with a benzyl-protected chi
tobiose unit was synthesized and used for the preparation of peptide thioes
ter with the sequence of Emmprin (34-58) by Boc strategy. C-Terminal peptid
e amide (59-94) was also prepared by the solid-phase method. These segments
were condensed by activation of the thioester group by silver ions to obta
in a protected form of Emmprin (34-94)-NH2. After deprotection and air oxid
ation, the desired Emmprin (34-94)-NH2 with chitobiose was successfully obt
ained. (C) 2001 Elsevier Science Ltd. All rights reserved.