Zampieri Niccolò, Xu Chong-Feng, Neubert Thomas A, Chao Moses V
Molecular Neurobiology Program, Skirball Institute for Biomolecular Medicine and Department of Cell Biology, New York University School of Medicine, New York, New York 10016, USA.
J Biol Chem. 2005 Apr 15;280(15):14563-71. doi: 10.1074/jbc.M412957200. Epub 2005 Feb 8.
The p75 neurotrophin receptor (p75(NTR)), a member of the tumor necrosis factor superfamily of receptors, undergoes multiple proteolytic cleavage events. These events are initiated by an alpha-secretase-mediated release of the extracellular domain followed by a gamma-secretase-mediated intramembrane cleavage. However, the specific determinants of p75(NTR) cleavage events are unknown. Many other substrates of gamma-secretase cleavage have been identified, including Notch, amyloid precursor protein, and ErbB4, indicating there is broad substrate recognition by gamma-secretase. Using a series of deletion mutations and chimeric receptors of p75(NTR) and the related Fas receptor, we have identified domains that are essential for p75(NTR) proteolysis. The initial alpha-secretase cleavage was extracellular to the transmembrane domain. Unfortunately, deletion mutants were not capable of defining the requirements of ectodomain shedding. Although this cleavage is promiscuous with respect to amino acid sequence, its position with respect to the transmembrane domain is invariant. The generation of chimeric receptors exchanging different domains of noncleavable Fas receptor with p75(NTR), however, revealed that a discrete domain above the membrane is sufficient for efficient cleavage of p75(NTR). Mass spectrometric analysis confirmed the cleavage can occur with a truncated p75(NTR) displaying only 15 extracellular amino acids in the stalk region.
p75神经营养因子受体(p75(NTR))是肿瘤坏死因子超家族受体的成员之一,会经历多次蛋白水解切割事件。这些事件由α-分泌酶介导的细胞外结构域释放引发,随后是γ-分泌酶介导的跨膜切割。然而,p75(NTR)切割事件的具体决定因素尚不清楚。γ-分泌酶切割的许多其他底物已被鉴定出来,包括Notch、淀粉样前体蛋白和ErbB4,这表明γ-分泌酶具有广泛的底物识别能力。通过一系列p75(NTR)的缺失突变和嵌合受体以及相关的Fas受体,我们确定了对p75(NTR)蛋白水解至关重要的结构域。最初的α-分泌酶切割发生在跨膜结构域的细胞外。不幸的是,缺失突变体无法确定胞外域脱落的要求。尽管这种切割在氨基酸序列方面具有随意性,但其相对于跨膜结构域的位置是不变的。然而,用p75(NTR)与不可切割的Fas受体交换不同结构域生成嵌合受体,结果表明膜上方的一个离散结构域足以有效切割p75(NTR)。质谱分析证实,仅在柄区显示15个细胞外氨基酸的截短型p75(NTR)也能发生切割。