Membrane type-1 matrix metalloprotein inhibitors and uses thereof
一种基质金属、膜型的技术,应用在蛋白酶抑制剂、肽/蛋白质成分、抗炎剂等方向
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Embodiment 1
[0262] Preparation of MT1-MMP-derived peptides
[0263] In carrying out the experiments described in the Examples below, the following peptides were prepared. First, a peptide with the sequence of the cytoplasmic domain of MT1-MMP (RRHGTPRRLLLYCQRSLLDKV; SEQ ID NO: 117) and a non-phosphorylatable form of this peptide (RRHGTPRRLLFCQRSLLDKV; SEQ ID NO: 118) were prepared, wherein in combination with human MT1- The tyrosine at the position corresponding to amino acid 573 of the MMP sequence was replaced by phenylalanine. This non-phosphorylatable peptide was referred to as "M-14".
[0264] Additionally, a peptide with the M-14 sequence fused to the third helix of the cell-penetrating tentaclepedin homology domain (RQIKIWFQNRRMKWKK; SEQ ID NO: 119) was made. This fusion peptide is called ACM-14 and has the sequence: Biotin-Ahx-RQIKIWFQNRRMKWKK-RRHGTPRRLLFCQRSLLDKV (SEQ ID NO: 176). A version of the fusion peptide in which the cytoplasmic MT1-MMP domain sequence was scrambled wa...
Embodiment 2
[0266] Expression of Y573F MT1-MMP inhibits tumor growth
[0267] HT1080 fibrosarcoma cells were stably transfected with WT MT1-MMP or Y573F MT1-MMP. HT1080 cells are very aggressive cancer cells that express elevated levels of MT1-MMP. These two groups of cells were transplanted subcutaneously into athymic nude mice, and tumor growth was monitored. Such as figure 2 As shown, cells expressing the cytoplasmic domain of MT1-MMP exhibited significant tumor growth, whereas no tumor growth was observed in mice receiving cells expressing the Y573F mutant.
Embodiment 3
[0269] ACM-14 and scACM-14 efficiently taken up by fibrosarcoma cells
[0270] To determine whether ACM-14 and scACM-14 were able to enter tumor cells, HT-1080 fibrosarcoma cells were incubated with each peptide (1 μM) for 1 hr, and peptide uptake was analyzed by immunofluorescence and confocal microscopy. Such as image 3 As shown, ACM-14 and its promiscuous form (scACM-14) were visualized in this cell, indicating efficient and rapid cellular uptake.
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