2KSA
Substance P in DMPC/CHAPS isotropic q=0.25 bicelles as a ligand for NK1R
2KSA の概要
| エントリーDOI | 10.2210/pdb2ksa/pdb |
| 関連するPDBエントリー | 2KS9 2KSB |
| NMR情報 | BMRB: 20116 |
| 分子名称 | Substance-P receptor, Substance P (2 entities in total) |
| 機能のキーワード | substance p, dmpc/chaps bicelle, autodock, nk1r, neuropeptide receptor-neuropeptide complex, neuropeptide receptor/neuropeptide |
| 由来する生物種 | Homo sapiens (human) 詳細 |
| タンパク質・核酸の鎖数 | 2 |
| 化学式量合計 | 43030.47 |
| 構造登録者 | |
| 主引用文献 | Gayen, A.,Goswami, S.K.,Mukhopadhyay, C. NMR evidence of GM1-induced conformational change of Substance P using isotropic bicelles Biochim.Biophys.Acta, 2010 Cited by PubMed Abstract: Substance P (SP) is one of the target neurotransmitters associated with diseases related to chronic inflammation, pain and depression. The selective receptor for SP, NK(1)R is located in the heterogeneous microdomains or caveolae in membrane. Gangliosides, specifically GM1, are markers of these heterogeneous sites. Also, gangliosides are considered as important regulatory elements in cell-cell recognition and cell signaling. In the present work, we describe the conformations of Substance P in the presence of ternary membrane systems containing GM1 at the physiological concentration. SP is mostly unstructured in water, but appears as extended 3(10) helical or turn III in isotropic bicelles, more pronounced in the presence of GM1. NMR results suggest that, in the GM1 containing bicelles, the peptide is more inserted into the membrane with its C-terminus, while N-terminus lies close to the membrane-water interface. The NMR-derived conformation of SP in GM1 bicelles is docked on homology modeled NK(1)R and resulting interactions satisfy reported mutagenesis, fluorescence, photo-affinity labeling and modeling data. The results highlight efficacy of GM1 in membrane in providing structure in an otherwise flexible neurotransmitter Substance P; thus providing indication that it may be useful also for other neurotransmitter peptides/proteins associated with membrane. PubMed: 20937248DOI: 10.1016/j.bbamem.2010.09.023 主引用文献が同じPDBエントリー |
| 実験手法 | SOLUTION NMR |
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