Institute of Organic Chemistry and Biochemistry, Czech Academy of Sciences, Flemingovo namesti 2, 160 00 Prague 6, Czech Republic.
Second Faculty of Medicine, Charles University, V Uvalu 84, 150 06 Prague 5, Czech Republic.
Int J Mol Sci. 2019 Sep 9;20(18):4430. doi: 10.3390/ijms20184430.
Transient receptor potential (TRPs) channels are crucial downstream targets of calcium signalling cascades. They can be modulated either by calcium itself and/or by calcium-binding proteins (CBPs). Intracellular messengers usually interact with binding domains present at the most variable TRP regions-N- and C-cytoplasmic termini. Calmodulin (CaM) is a calcium-dependent cytosolic protein serving as a modulator of most transmembrane receptors. Although CaM-binding domains are widespread within intracellular parts of TRPs, no such binding domain has been characterised at the TRP melastatin member-the transient receptor potential melastatin 6 (TRPM6) channel. Another CBP, the S100 calcium-binding protein A1 (S100A1), is also known for its modulatory activities towards receptors. S100A1 commonly shares a CaM-binding domain. Here, we present the first identified CaM and S100A1 binding sites at the N-terminal of TRPM6. We have confirmed the L520-R535 N-terminal TRPM6 domain as a shared binding site for CaM and S100A1 using biophysical and molecular modelling methods. A specific domain of basic amino acid residues (R526/R531/K532/R535) present at this TRPM6 domain has been identified as crucial to maintain non-covalent interactions with the ligands. Our data unambiguously confirm that CaM and S100A1 share the same binding domain at the TRPM6 N-terminus although the ligand-binding mechanism is different.
瞬时受体电位 (TRP) 通道是钙信号级联的关键下游靶标。它们可以通过钙本身和/或钙结合蛋白 (CBP) 进行调节。细胞内信使通常与位于 TRP 最可变的 N-和 C-细胞质末端的结合域相互作用。钙调蛋白 (CaM) 是一种钙依赖性细胞溶质蛋白,作为大多数跨膜受体的调节剂。尽管 CaM 结合域广泛存在于 TRP 的细胞内部分,但在 TRP 金属蛋白酶 6 (TRPM6) 通道中尚未表征这种结合域。另一种 CBP,即 S100 钙结合蛋白 A1 (S100A1),也因其对受体的调节活性而闻名。S100A1 通常具有与 CaM 结合的结构域。在这里,我们首次在 TRPM6 的 N 端鉴定出 CaM 和 S100A1 结合位点。我们使用生物物理和分子建模方法证实了 L520-R535 N 端 TRPM6 结构域是 CaM 和 S100A1 的共同结合位点。该 TRPM6 结构域上存在的碱性氨基酸残基 (R526/R531/K532/R535) 的特定结构域已被确定为与配体保持非共价相互作用的关键。我们的数据明确证实 CaM 和 S100A1 在 TRPM6 N 端共享相同的结合域,尽管配体结合机制不同。