Harding P J, Attrill H, Ross S, Koeppe J R, Kapanidis A N, Watts A
Biomembrane Structure Unit, Department of Biochemistry, University of Oxford, South Parks Road, Oxford, OX1 3QU, U.K.
Biochem Soc Trans. 2007 Aug;35(Pt 4):760-3. doi: 10.1042/BST0350760.
NT (neurotensin) is an endogenous tridecapeptide neurotransmitter found in the central nervous system and gastrointestinal tract. One receptor for NT, NTS1, belongs to the GPCR (G-protein-coupled receptor) superfamily, has seven putative transmembrane domains, and is being studied by a range of single-molecule, functional and structural approaches. To enable biophysical characterization, sufficient quantities of the receptor need to be expressed and purified in an active form. To this end, rat NTS1 has been expressed in Escherichia coli in an active ligand-binding form at the cell membrane and purified in sufficient amounts for structural biology studies either with or without fluorescent protein [YFP (yellow fluorescent protein) and CFP (cyan fluorescent protein)] fusions. Ligand binding has been demonstrated in a novel SPR (surface plasmon resonance) approach, as well as by conventional radioligand binding measurements. These improvements in production of NTS1 now open up the possibility of direct structural studies, such as solid-state NMR to interrogate the NT-binding site, EM (electron microscopy), and X-ray crystallography and NMR.
神经降压素(NT)是一种内源性十三肽神经递质,存在于中枢神经系统和胃肠道中。NT的一种受体NTS1属于G蛋白偶联受体(GPCR)超家族,具有七个假定的跨膜结构域,目前正通过一系列单分子、功能和结构方法进行研究。为了进行生物物理表征,需要以活性形式表达和纯化足够数量的受体。为此,大鼠NTS1已在大肠杆菌中以活性配体结合形式表达于细胞膜上,并已纯化出足够数量用于结构生物学研究,无论是否有荧光蛋白[黄色荧光蛋白(YFP)和青色荧光蛋白(CFP)]融合。配体结合已通过一种新型表面等离子体共振(SPR)方法以及传统的放射性配体结合测量得到证实。NTS1生产方面的这些改进现在为直接结构研究开辟了可能性,例如通过固态核磁共振来探究NT结合位点、电子显微镜(EM)以及X射线晶体学和核磁共振。