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. 2010 Jun 21;285(35):27265–27278. doi: 10.1074/jbc.M110.113647

FIGURE 5.

FIGURE 5.

Oligomerization of human AChE, BChE, and mutants lacking the C-terminal t-peptide or containing exchanged t-peptides. A, comparison of the amino acid sequences of C-terminal t-peptides from human AChE and BChE. Identical residues are indicated by asterisks. Highly and moderately similar residues are indicated by double dots and single dots, respectively. B, schematic representations of AChET, BChET, and their mutants. AChET and BChET are wild-type human AChE and BChE, respectively. AChEΔT and BChEΔT are mutants in which the t-peptides were deleted. AChEBChE-T and BChEAChE-T are chimeras in which the t-peptides of AChE and BChE were exchanged. C, HEK293T cells were transfected with cDNAs encoding AChET, AChEΔT, AChEBChE-T, BChET, BChEΔT, or BChEAChE-T with and without cDNA encoding PRiMA for 2 days. Cell extracts containing equal amounts of enzymatic activity were subjected to sucrose density gradient analysis as in Fig. 1A. The positions of the peaks corresponding to the G1, G2, and G4a forms of AChE (left panel) and BChE (right panel) are shown by vertical dashed lines. Enzymatic activities are expressed in arbitrary units, and one representative result is shown (n = 4).