Liepinsh E, Ilag L L, Otting G, Ibáñez C F
Department of Medical Biochemistry and Biophysics, Karolinska Institute, Stockholm, Sweden.
EMBO J. 1997 Aug 15;16(16):4999-5005. doi: 10.1093/emboj/16.16.4999.
The intracellular domain of the p75 neurotrophin receptor (p75ICD) lacks catalytic activity but contains a motif similar to death domains found in the cytoplasmic regions of members of the tumor necrosis factor receptor family and their downstream targets. Although some aspects of the signaling pathways downstream of p75 have been elucidated recently, mechanisms of receptor activation and proximal signaling events are unknown. Here we report the nuclear magnetic resonance (NMR) structure of the 145 residue long p75ICD. The death domain of p75ICD consists of two perpendicular sets of three helices packed into a globular structure. The polypeptide segment connecting the transmembrane and death domains as well as the serine/threonine-rich C-terminal end are highly flexible in p75ICD. Unlike the death domains involved in signaling by the TNF receptor and Fas, p75ICD does not self-associate in solution. A surface area devoid of charged residues in the p75ICD death domain may indicate a potential site of interaction with downstream targets.
p75神经营养因子受体的细胞内结构域(p75ICD)缺乏催化活性,但包含一个与肿瘤坏死因子受体家族成员及其下游靶点的细胞质区域中发现的死亡结构域相似的基序。尽管最近已经阐明了p75下游信号通路的一些方面,但受体激活机制和近端信号事件尚不清楚。在此,我们报道了145个残基长的p75ICD的核磁共振(NMR)结构。p75ICD的死亡结构域由两组相互垂直的三个螺旋组成,堆积成球状结构。在p75ICD中,连接跨膜结构域和死亡结构域的多肽片段以及富含丝氨酸/苏氨酸的C末端非常灵活。与参与TNF受体和Fas信号传导的死亡结构域不同,p75ICD在溶液中不会自我缔合。p75ICD死亡结构域中一个没有带电残基的表面区域可能表明其与下游靶点相互作用的潜在位点。