Bedoukian   RussellIPM   RussellIPM   Piezoelectric Micro-Sprayer


Home
Animal Taxa
Plant Taxa
Semiochemicals
Floral Compounds
Semiochemical Detail
Semiochemicals & Taxa
Synthesis
Control
Invasive spp.
References

Abstract

Guide

Alphascents
Pherobio
InsectScience
E-Econex
Counterpart-Semiochemicals
Print
Email to a Friend
Kindly Donate for The Pherobase

« Previous Abstract"RAM2, an essential gene of yeast, and RAM1 encode the two polypeptide components of the farnesyltransferase that prenylates a-factor and Ras proteins"    Next AbstractUnexpected increase in indoor pollutants after the introduction of a smoke-free policy in a correctional center »

Arch Biochem Biophys


Title:"Production of the rat complement regulator, Crry, as an active soluble protein in Pichia pastoris"
Author(s):He C; Alexander JJ; Lim A; Quigg RJ;
Address:"Department of Medicine, University of Chicago, Illinois 60637, USA"
Journal Title:Arch Biochem Biophys
Year:1997
Volume:341
Issue:2
Page Number:347 - 352
DOI: 10.1006/abbi.1997.9989
ISSN/ISBN:0003-9861 (Print) 0003-9861 (Linking)
Abstract:"In this report, we describe the use of the methylotrophic yeast Pichia pastoris for the production of the rat complement regulator, Crry. Crry normally exists as an intrinsic membrane protein containing six to seven short consensus repeats (SCRs), a transmembrane region, and a cytoplasmic tail. To produce Crry as a soluble recombinant protein, nucleotides encoding the five N-terminal SCRs from the rat Crry cDNA were amplified by PCR, and cloned into the P. pastoris expression vector, pPIC9. This vector contains the yeast alpha-factor signal sequence, thereby leading to secretion of recombinant protein. This construct was subsequently integrated into P. pastoris strain GS115 genomic DNA. Secreted soluble Crry was produced by induction of the AOX1 promoter with methanol. Recombinant Crry protein was purified to homogeneity by sequential Mono Q and Mono P chromatography. The protein was highly active toward the alternative and classical pathways of complement, inhibiting the latter by approximately 90% at a concentration of 15 nM. The P. pastoris system offers an efficient method for the production of soluble recombinant Crry. Production of active rat Crry offers opportunities to study long-term models of disease in rats, which has not been possible with available heterologous complement inhibitors"
Keywords:"Animals Antigens, Surface DNA, Recombinant Genetic Vectors Mating Factor Peptides/genetics/physiology Pichia/*metabolism Protein Sorting Signals/genetics/physiology Rats Receptors, Cell Surface Receptors, Complement/*biosynthesis/genetics Recombinant Fusi;"
Notes:"MedlineHe, C Alexander, J J Lim, A Quigg, R J eng DK 07510/DK/NIDDK NIH HHS/ DK 41873/DK/NIDDK NIH HHS/ Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S. 1997/05/15 Arch Biochem Biophys. 1997 May 15; 341(2):347-52. doi: 10.1006/abbi.1997.9989"

 
Back to top
 
Citation: El-Sayed AM 2024. The Pherobase: Database of Pheromones and Semiochemicals. <http://www.pherobase.com>.
© 2003-2024 The Pherobase - Extensive Database of Pheromones and Semiochemicals. Ashraf M. El-Sayed.
Page created on 03-07-2024