Resonance energy transfer assay with synaptobrevin substrate moiety
Compositions and methods for analyzing intracellular BoNT protease activity, and especially BoNT/B, BoNT/G, BoNT/D, and/or BoNT/F protease activity are provided. Most preferably, cells express one or more recombinant hybrid proteins that include one or more fluorescent proteins and at least one BoNT protease recognition and cleavage sequence, and analysis is performed using FRET analysis.
1. A cell-based method of measuring protease activity of a Botulinum neurotoxin (BoNT) protease, comprising:
providing a transfected cell that produces a hybrid protein comprising a structure of A-B-C-D; wherein A is a transmembrane domain from synaptobrevin targeted to an intracellular vesicle membrane and is not cleavable by said BoNT protease, B is a first fluorescent protein, C is a BoNT protease recognition and cleavage sequence, and D is a second fluorescent protein selected to form a Forster resonance energy transfer (FRET) pair with said first fluorescent protein, and wherein a peptide spacer is disposed between one or more of C and B and C and D, wherein said peptide spacer and said BoNT protease recognition and cleavage sequence are selected to support FRET between said first fluorescent protein and said second fluorescent protein;
contacting said transfected cell with said BoNT protease under conditions to take up the BoNT protease by said transfected cell; and
measuring FRET between said first and second fluorescent proteins in said transfected cell.
2. The method of claim 1 , wherein said transfected cell is a cell selected from the group consisting of a neuronal cell, a neuroendocrine tumor cell, a hybrid cell, and a stem cell.
3. The method of claim 1 , wherein C comprises at least two of a BoNT/B, a BoNT/G, a BoNT/D, and a BoNT/F protease recognition and cleavage sequence.
4. The method of claim 1 , wherein C is a portion of synaptobrevin.
5. The method of claim 1 , wherein said peptide spacer comprises a length of equal to or less than 12 amino acids.
6. The method of claim 1 , further comprising a step of contacting said transfected cell with a putative BoNT inhibitor prior to contacting said transfected cell with said BoNT protease.
7. The method of claim 1 , wherein said hybrid protein having the structure of A-B-C-D comprises the amino acid sequence of SEQ ID NO: 2.
8. A cell-based method of measuring protease activity of a Botulinum neurotoxin (BoNT) protease, comprising:
providing a transfected cell that produces a first hybrid protein having a structure of A-C-B and a second hybrid protein having a structure of A-C-D; wherein A is a transmembrane domain of synaptobrevin targeted to an intracellular vesicle membrane and is not cleavable by said BoNT protease, B is a first fluorescent protein, C is a BoNT protease recognition and cleavage sequence, and D is a second fluorescent selected to form a FRET pair with said first fluorescent protein, wherein a peptide spacer is disposed between one or more of A and C, C and B, and C and D, wherein said transmembrane domain, said peptide spacer, and said BoNT protease recognition and cleavage sequence are selected to support FRET between said first fluorescent protein and said second fluorescent protein when said first hybrid protein and said second hybrid protein are collocated with a vesicle;
contacting said transfected cell with said BoNT protease under conditions to take up said BoNT protease by said transfected cell; and
measuring FRET between said first and second fluorescent proteins in said transfected cell.
9. The method of claim 8 , wherein said first hybrid protein comprises the amino acid sequence of SEQ ID NO: 4, and wherein said second hybrid protein comprises the amino acid sequence of SEQ ID NO: 6.
10. The method of claim 8 , wherein said transfected cell is a cell selected from the group consisting of a neuronal cell, a neuroendocrine tumor cell, a hybrid cell, and a stem cell.
11. The method of claim 8 , wherein C comprises at least two of a BoNT/B, a BoNT/G, a BoNT/D, and a BoNT/F protease recognition and cleavage sequence.
12. The method of claim 8 , wherein C is a portion of synaptobrevin.
13. The method of claim 8 , wherein said peptide spacer comprises a length of equal to or less than 12 amino acids.
14. The method of claim 8 , further comprising a step of contacting said transfected cell with a putative BoNT inhibitor prior to contacting said transfected cell with said BoNT protease.