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. 2010 Aug 6;285(43):33307–33314. doi: 10.1074/jbc.M110.153940

FIGURE 1.

FIGURE 1.

The S0-S1 linker is palmitoylated in BK channels. A, schematic illustrating the topology of the BK channel pore-forming α-subunit. Sequence alignments of cysteine residues in the S0-S1 linker indicate evolutionary conservation (gray box) across vertebrates, Drosophila and C. elegans. Murine sequence numbered starting from the initiation methionine (MDALI), accession number: AF156674. CSS-Palm prediction scores were determined with the CSS-Palm v2.0 platform. B, representative fluorographs (upper) and Western blots (lower) of full-length ZERO-HA channels and ZERO channels with mutation of key cysteine residues in the S0-S1 linker, expressed in HEK293 cells. Constructs were labeled with [3H]palmitate for 4 h and immunoprecipitated (IP) by using α-HA magnetic microbeads and detected by fluorography. Ratios (normalized to the wild-type ZERO channel) of [3H]palmitate detection in comparison to total protein expression are included.