Download Intramembrane-Cleaving Proteases (I-CLiPs) (Proteases in by Nigel M. Hooper (Editor), Uwe Lendeckel (Editor) PDF

By Nigel M. Hooper (Editor), Uwe Lendeckel (Editor)

In recent times increasingly more proteases were pointed out that catalyse peptide bond hydrolysis within the aircraft of the mobile membrane. those so-called intramembrane-cleaving proteases (I-CLiPs) are all in favour of a various variety of mobile methods, together with phone rules, signalling, quorum sensing, protein processing, lipid metabolism and the spread out protein reaction. a few I-CLiPs play severe roles in illnesses corresponding to Alzheimer s and viral an infection. The authors, who're all global leaders during this fascinating box of cellphone biology, supply an outline of a number of the proteases together with contemporary info derived from the structural decision of a few of the I-CliPs, and talk about many of the roles that those proteases play in biology and disorder. the purpose of this e-book is to supply an replace in this rising staff of bizarre yet vital proteases for either the professional and people with a broader curiosity in proteases. among the objective viewers should be protease researchers, enzymologists, these operating in academia and the pharmaceutical on organic procedures and illnesses related to I-CLiPs.

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Extra info for Intramembrane-Cleaving Proteases (I-CLiPs) (Proteases in Biology and Disease)

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Louvi A. and Artavanis-Tsakonas S. (2006) Notch signalling in vertebrate neural development. Nat Rev Neurosci 7, 93–102. 28 GOLDE ET AL. , Bolduc M. and Leclerc D. (2005) Signal peptide peptidase promotes the formation of hepatitis C virus non-enveloped particles and is captured on the viral membrane during assembly. J Gen Virol 86, 3055–3064. , Wen P. , Siman R. and Robakis N. K. (2003) A CBP binding transcriptional repressor produced by the PS1/epsilon-cleavage of N-cadherin is inhibited by PS1 FAD mutations.

2005; Krawitz et al. 2005). No mouse knockouts have been reported. These studies suggest that SPP and its homologs have important functional roles in development. In C. elegans, deficiency of ce-imp-2 (a SPP like gene) causes a severe developmental phenotype (Grigorenko et al. 2004). The effect of knockout of the two other C. elegans SPP homologs was not reported. Drosophila deficient in one of two SPP genes (CG11840) had defective trachea and died as larvae (Casso et al. 2005). In Zebrafish, when either the SPP or SPPL3 homologs were knocked down, an embryonic lethal phenotype was observed, with 24 GOLDE ET AL.

2004). Assembly of these -secretase complexes is tightly regulated in a coordinated manner. The available data suggest a model for -secretase complex assembly where first NCT and APH-1 form an initial complex (LaVoie et al. 2003). In the next step of assembly PS joins this NCT/APH-1 assembly intermediate to form a ternary complex. Finally PEN-2 assembles to trigger PS endoproteolysis into its NTF and CTF (Takasugi et al. 2003). Following these assembly steps which take place at the endoplasmic reticulum (Kim et al.

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