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In vivo localisation and stability of human Mcl-1 using green fluorescent protein (GFP) fusion proteins.
- Source :
-
FEBS letters [FEBS Lett] 2000 Jul 28; Vol. 478 (1-2), pp. 72-6. - Publication Year :
- 2000
-
Abstract
- Mcl-1 is an anti-apoptotic member of the Bcl-2 family of proteins. We have expressed full length and mutated GFP:Mcl-1 fusion proteins to define structural motifs that control protein localisation and stability. When expressed in U-937 cells, full length Mcl-1 locates primarily within mitochondria and its half-life was approximately 3 h, which was identical to the native, endogenously expressed protein. When the terminal 20 amino acids from the C-terminus of the protein were detected, the protein was diffused in the cytoplasm, but its stability was unaffected. This confirms that this region is responsible for efficient targeting to mitochondria. Surprisingly, deletion of 104 amino acids (residues 79-183) that contain putative PEST sequences and other stability regulating motifs, did not affect protein stability.
- Subjects :
- Amino Acid Motifs
Biological Transport
Blotting, Western
Cytoplasm metabolism
Green Fluorescent Proteins
Half-Life
Humans
Luminescent Proteins genetics
Luminescent Proteins metabolism
Mitochondria metabolism
Myeloid Cell Leukemia Sequence 1 Protein
Neoplasm Proteins chemistry
Neoplasm Proteins genetics
Recombinant Fusion Proteins chemistry
Recombinant Fusion Proteins genetics
Sequence Deletion
Thermodynamics
Transfection
U937 Cells
Neoplasm Proteins metabolism
Protein Sorting Signals genetics
Protein Sorting Signals physiology
Proto-Oncogene Proteins c-bcl-2
Recombinant Fusion Proteins metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 0014-5793
- Volume :
- 478
- Issue :
- 1-2
- Database :
- MEDLINE
- Journal :
- FEBS letters
- Publication Type :
- Academic Journal
- Accession number :
- 10922472
- Full Text :
- https://doi.org/10.1016/s0014-5793(00)01809-3