Antiproliferative effect of pHLIP-amanitin.
Antiproliferative effect of pHLIP-amanitin.
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DOI:
10.1021/bi301647y
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发表时间:
2013-02-19
期刊:
影响因子:
2.9
通讯作者:
Reshetnyak YK
中科院分区:
文献类型:
--
作者:
Moshnikova A;Moshnikova V;Andreev OA;Reshetnyak YK
Toxins could be effective anti-cancer drugs, if their selective delivery into cancer cells could be achieved. We have shown that the energy of membrane associated-folding of water-soluble membrane peptides of pHLIP® (pH Low Insertion Peptide) family could be used to move cell-impermeable cargoes across the lipid bilayer in cytoplasm of cancer cells. Here we present the results of a study of pHLIP-mediated cellular delivery of a polar cell-impermeable toxin, α-amanitin, inhibitor of RNA polymerase II. We show that pHLIP can deliver α-amanitin into cells in a pH-dependent fashion and induce cell death within 48 hours. Translocation capability could be tuned by conjugating amanitin to the C-terminus of pHLIP via linkers of different hydrophobicity cleavable in cytoplasm. pHLIP-SPDP-amanitin, which exhibits 4–5 times higher anti-proliferative ability at pH 6 compare to pH 7.4, was selected as the best construct. The major mechanism of amanitin delivery is direct translocation (flip) across a membrane by pHLIP and cleavage of S-S bond in a cytoplasm. Anti-proliferative effect was monitored on four different human cancer cell lines. pHLIP-mediated cytoplasmic delivery of amanitin could open great opportunities to use the toxin as a potent pH-selective anti-cancer agent, which predominantly targets highly-proliferative cancer cells with low extracellular pH.
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影响因子:
10.3
作者:
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通讯作者:
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影响因子:
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DOI:
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发表时间:
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作者:
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通讯作者:
Thompson, David H.