Tag and release: strategies for the intracellular cleavage of protein conjugates

被引:9
作者
Baumann, Alice Leonie [1 ,2 ]
Hackenberger, Christian Peter Richard [1 ,2 ]
机构
[1] Leibniz Forschungsinst Mol Pharmakol Forschungsve, Campus Berlin Buch,Robert Roessle Str 10, D-13125 Berlin, Germany
[2] Humboldt Univ, Inst Chem, Brook Taylor Str 2, D-12489 Berlin, Germany
关键词
TRIGGERED DRUG-RELEASE; DOXORUBICIN; ACTIVATION; CHEMISTRY; DELIVERY; PRODRUGS; CLICK; MODEL; PH; OPTIMIZATION;
D O I
10.1016/j.cbpa.2019.04.019
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Attaching a functional moiety to a protein is required for a wealth of applications, comprising targeted delivery, controlling of enzyme activity, and prodrug-based therapy. Targeting intracellular processes requires the cellular delivery of the protein. While at first, a stable connection between the protein and the modification is desired, once inside the cell, the conjugate might be cleaved again to restore or activate the function of the individual parts. This can be achieved by employing cleavable linkages in conjugates, which are responsive to chemical or enzymatic stimuli inside cells. In this overview we describe strategies, how such entities can be introduced into proteins and how selective intracellular cleavage can be accomplished.
引用
收藏
页码:39 / 46
页数:8
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