Peptides and calcium regulation in mammalian cells
View Patent ↗Calcium channels in a variety of tissues may contain different subunits, including several different γ (gamma) subunits. We report studies regarding structural features of certain gamma subunits, for example the N-terminal first transmembrane domain (TM1) of the subunit γ6. We disclose that certain structural motifs, for example a GxxxG-like structural motif as described herein, can mediate subunit function for calcium channels. A particular peptide motif that has been identified as significant for the ability to mediate a decrease in calcium current is GxxxA. Compositions and methods are disclosed which are useful in modifying calcium regulation in mammalian cells. In various embodiments, calcium current is modified.
1. An isolated calcium channel gamma6 subunit peptide fragment comprising an N-terminal first transmembrane domain segment of at least 15 continuous amino acids of a rat, mouse, or human source; wherein the peptide fragment has a maximum total length of 15 to 40 amino acids, and wherein the segment comprises a Gx 2 x 3 x 4 G-like structural motif located near the cytoplasmic end of the first transmembrane domain, wherein the Gx 2 x 3 x 4 G-like motif is a x 1 x 2 x 3 x 4 x 5 in which x 1 and x 5 are each independently glycine or alanine or serine and wherein x 2 , x 3 , and x 4 are each independently selected from leucine, valine, phenylalanine, glycine, threonine, isoleucine, alanine and serine, and wherein said peptide fragment can reduce voltage dependent calcium current in a cell.
2. The peptide fragment of claim 1 having a maximum total length of 15 amino acids.
3. The peptide fragment of claim 1 having a maximum total length of about 20 amino acids.
4. The peptide fragment of claim 1 having a homology level of at least 90% to the N-terminal first transmembrane domain segment of a gamma6 (γ 6 ) subunit amino acid sequence from a human source.
5. The peptide fragment of claim 1 having a homology level of at least 90% to the N-terminal first transmembrane domain segment of a γ 6 subunit amino acid sequence from a rat source.
6. The peptide fragment of claim 1 having a homology level of at least 90% to the N-terminal first transmembrane domain segment of a γ 6 subunit amino acid sequence from a mouse source.
7. The peptide fragment of claim 1 wherein x 1 and x 5 are glycine and alanine respectively.
8. The peptide fragment of claim 1 wherein X1 is glycine.
9. The peptide fragment of claim 1 having a structural groove along at least a portion of a three-dimensional projection of a helical face of the first transmembrane domain of the peptide.
10. A method of modifying an ability of a calcium channel to regulate calcium in a cell, comprising exposing said cell to the calcium channel gamma6 subunit peptide fragment of claim 1 .
11. A method of decreasing calcium current in a cell, comprising exposing said cell to the calcium channel gamma6 subunit peptide fragment of claim 1 .
12. The method of claim 11 , wherein said exposing step comprises recombinantly expressing said peptide fragment within said cell.
13. The peptide fragment of claim 1 wherein the N-terminal first transmembrane domain segment has the sequence of SEQ ID NO: 12 or a sequence at least 90% homologous to SEQ ID NO: 12.
14. The peptide fragment of claim 1 having a homology level of at least 90% to the N-terminal first transmembrane domain segment of a gamma6 subunit amino acid sequence from a human, rat, or mouse source.