Dennis Patrick B, Mercer Carol A
University of Cincinnati, Genome Research Institute, Department of Cancer and Cell Biology, Cincinnati, Ohio, USA.
Methods Enzymol. 2009;452:97-118. doi: 10.1016/S0076-6879(08)03607-0.
The endpoint of the autophagic process is the breakdown of delivered cytoplasmic cargo in lysosomes. Therefore, assays based on degradation of cargo are of particular interest in that they can measure regulation of the entire autophagic process, including changes in cargo delivery and breakdown in the lytic compartment. Betaine homocysteine methyltransferase (BHMT) is one of many cytosolic proteins found in the mammalian autophagosome, and delivery of BHMT to the lysosome results in its proteolysis to discrete fragments under certain conditions. Making use of these observations, the GST-BHMT assay was developed as an endpoint, cargo-based autophagy assay. Using this assay as a starting point, additional cargo-based assays have been developed with the potential to measure autophagic degradation of specific subcellular compartments. Here we describe the development and validation of these assays.
自噬过程的终点是溶酶体中所运送的细胞质货物的降解。因此,基于货物降解的检测方法特别受关注,因为它们能够测量整个自噬过程的调控情况,包括货物运送的变化以及在溶酶体中的降解情况。甜菜碱同型半胱氨酸甲基转移酶(BHMT)是在哺乳动物自噬体中发现的众多胞质蛋白之一,在特定条件下,BHMT被运送至溶酶体后会被蛋白水解成离散的片段。基于这些观察结果,开发了GST-BHMT检测法作为一种基于货物的自噬终点检测法。以该检测法为起点,又开发了其他基于货物的检测方法,这些方法有可能用于测量特定亚细胞区室的自噬降解。在此,我们描述这些检测方法的开发与验证过程。