Chemistry and Biochemistry, University of California, Los Angeles, Los Angeles, California, 90095, USA.
Chembiochem. 2021 Dec 2;22(23):3277-3282. doi: 10.1002/cbic.202100379. Epub 2021 Sep 23.
Endosomal escape continues to be a limiting factor in the therapeutic use of nanomaterials. Assays to visualize endosomal escape often do not decouple the endosomal/lysosomal disruption from the release of payload into the cytosol. Here, we discuss three approaches to directly probe endosomal/lysosomal rupture: calcein dye dilution, lysosome size quantification and endosome/lysosome membrane integrity visualized with a genetically engineered cell line. We apply the three assays to endosomes/lysosomes ruptured via osmotic pressure and photochemical internalization.
内体逃逸仍然是纳米材料治疗应用的一个限制因素。用于可视化内体逃逸的测定方法通常不能将内体/溶酶体的破坏与有效载荷释放到细胞质中分开。在这里,我们讨论了三种直接探测内体/溶酶体破裂的方法:钙黄绿素染料稀释、溶酶体大小定量以及使用基因工程细胞系可视化内体/溶酶体膜的完整性。我们将这三种测定方法应用于通过渗透压和光化学内化破裂的内体/溶酶体。