Anilkumar Narayanapanicker, Uekita Takamasa, Couchman John R, Nagase Hideaki, Seiki Motoharu, Itoh Yoshifumi
Department of Matrix Biology, Kennedy Institute of Rheumatology Division, Imperial College London, London, UK.
FASEB J. 2005 Aug;19(10):1326-8. doi: 10.1096/fj.04-3651fje. Epub 2005 Jun 9.
MT1-MMP is a type I transmembrane proteinase that promotes cell migration and invasion. Here, we report that MT1-MMP is palmitoylated at Cys574 in the cytoplasmic domain, and this lipid modification is critical for its promotion of cell migration and clathrin-mediated internalization. The palmitoylation-defective mutant (C574A) failed to promote cell migration and was not internalized through clathrin pathway like wild-type, but it was internalized through the caveolae pathway. Reintroducing a cysteine at different positions in the cytoplasmic tail of the C574A mutant revealed that the position of the palmitoylated cysteine relative to LLY573, a motif that interacts with mu2 subunit of adaptor protein 2, is critical for the cell motility-promoting activity of MT1-MMP and its clathrin-mediated internalization. Taken together, palmitoylation of MT1-MMP is one of the key posttranslational modifications that determines MT1-MMP-dependent cell migration.
基质金属蛋白酶1(MT1-MMP)是一种促进细胞迁移和侵袭的I型跨膜蛋白酶。在此,我们报道MT1-MMP在其胞质结构域的半胱氨酸574处发生棕榈酰化,这种脂质修饰对其促进细胞迁移和网格蛋白介导的内化至关重要。棕榈酰化缺陷型突变体(C574A)无法促进细胞迁移,且不像野生型那样通过网格蛋白途径内化,但它可通过小窝途径内化。在C574A突变体的胞质尾部不同位置重新引入半胱氨酸后发现,棕榈酰化半胱氨酸相对于与衔接蛋白2的μ2亚基相互作用的基序LLY573的位置,对MT1-MMP的细胞运动促进活性及其网格蛋白介导的内化至关重要。综上所述,MT1-MMP的棕榈酰化是决定MT1-MMP依赖性细胞迁移的关键翻译后修饰之一。