Site-specific PEGylation of lidamycin and its antitumor activity

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Site-specific PEGylation of lidamycin and its antitumor activity

In this study, N-terminal site-specific mono-PEGylation of the recombinant lidamycin apoprotein (rLDP) of lidamycin (LDM) was prepared using a polyethyleneglycol (PEG) derivative (M w 20 kDa) through a reactive terminal aldehyde group under weak acidic conditions (pH 5.5). The biochemical properties of mPEG-rLDP-AE, an enediyne-integrated conjugate, were analyzed by SDS-PAGE, RP-HPLC, SEC-HPLC ...

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ژورنال

عنوان ژورنال: Acta Pharmaceutica Sinica B

سال: 2015

ISSN: 2211-3835

DOI: 10.1016/j.apsb.2015.03.006