RRC ID 61450
著者 Tabata A, Ohkubo Y, Tamura M, Tomoyasu T, Ohkura K, Nagamune H.
タイトル Construction of an improved drug delivery system tool with enhanced versatility in cell-targeting.
ジャーナル Anticancer Res
Abstract BACKGROUND/AIM:The aim of this study was to develop an improved drug delivery system (DDS) tool with enhanced versatility in the cell-targeting step using as Z-domain, a modified IgG binding domain of protein A from Staphylococcus aureus, as an IgG adapter domain.
MATERIALS AND METHODS:The chimera protein expression system composed of the Z-domain and chimeric cholesterol-dependent cytolysin mutant named His-Z-CDC(ss)(IS) was constructed in Escherichia coli. His-Z-CDC(ss)(IS) was purified by Ni-affinity chromatography, and its abilities for controlled pore formation, membrane binding, IgG binding, and target cell-specific delivery of liposomes carrying medicine were investigated.
RESULTS AND DISCUSSION:His-Z-CDC(ss)(IS) purified by Ni-affinity chromatography indicated pore-forming activity only under disulfide bond reducing conditions. His-Z-CDC(ss)(IS) also demonstrated an ability to bind both IgG and cholesterol-embedded liposomes via its Z-domain and domain 4, respectively. Furthermore, anticarcinoembryonic antigen (CEA) IgG-bound His-Z-CDC(ss)(IS) indicated effective delivery of liposomes carrying drugs to CEA-expressing cells.
CONCLUSION:His-Z-CDC(ss)(IS) was revealed to be an improved DDS tool with enhanced versatility in cell targeting.
巻・号 33(7)
ページ 2905-10
公開日 2013-7-1
PII 33/7/2905
PMID 23780978
MeSH Carcinoembryonic Antigen / metabolism* Cell Membrane / drug effects Cell Membrane / metabolism Cells, Cultured Cholesterol / metabolism Drug Delivery Systems* Fibroblasts / metabolism* Fluorouracil / administration & dosage Hemolysis / drug effects Hep G2 Cells / metabolism* Humans Immunoglobulin G / metabolism Liposomes* Perforin / genetics Perforin / metabolism* Protein Transport Recombinant Fusion Proteins / metabolism* Staphylococcus aureus
IF 1.994
リソース情報
ヒト・動物細胞 NB1RGB(RCB0222)