Jagged-1 juxtamembrane region: Biochemical characterization and cleavage by ADAM17 (TACE) catalytic domain

被引:12
作者
Coglievina, Maristella [1 ]
Guarnaccia, Corrado [1 ]
Zlatev, Ventsislav [1 ]
Pongor, Sandor [1 ]
Pintar, Alessandro [1 ]
机构
[1] ICGEB, Prot Struct & Bioinformat Grp, I-34149 Trieste, Italy
关键词
Notch signaling; Ectodomain shedding; Alagille syndrome; Metalloprotease; Circular dichroism; Mass spectrometry; CONVERTING-ENZYME TACE; ALAGILLE-SYNDROME; METALLOPROTEINASE; SECRETASE;
D O I
10.1016/j.bbrc.2013.02.022
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Ectodomain shedding of membrane receptors and ligands carried out by ADAMs (A disintegrin and metalloprotease) plays a major role in several signaling pathways, including Notch. The grounds of substrate recognition, however, are poorly understood. We demonstrate that a recombinant protein corresponding to the juxtamembrane region of Jagged-1, one of the Notch ligands, behaves as a structured module and is cleaved by ADAM17 catalytic domain at El054. A short synthetic peptide is cleaved at the same site but at a much higher rate, implying that the structure of the cleavage site in the native protein is a key determinant for substrate recognition. We also show that an Alagille syndrome-associated mutation near E1054 increases the cleavage rate, which suggests that this mutation may lead to an unbalance in Notch signaling due to a higher level of Jagged-1 shedding. (C) 2013 Elsevier Inc. All rights reserved.
引用
收藏
页码:666 / 671
页数:6
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