Bridging the gap: a GFP-based strategy for overexpression and purification of membrane proteins with intra and extracellular C-termini.
about
An efficient strategy for small-scale screening and production of archaeal membrane transport proteins in Escherichia coliMembrane protein structure determination using crystallography and lipidic mesophases: recent advances and successes.Biosynthesis and translocation of unsulfated acyltrehaloses in Mycobacterium tuberculosis.Fluorescent probe for high-throughput screening of membrane protein expressionGFP-based evaluation system of recombinant expression through the secretory pathway in insect cells and its application to the extracellular domains of class C GPCRsA Versatile Strategy for Production of Membrane Proteins with Diverse Topologies: Application to Investigation of Bacterial Homologues of Human Divalent Metal Ion and Nucleoside Transporters.Characterization and purification of a Na+/Ca2+ exchanger from an archaebacterium.Tricks of the trade used to accelerate high-resolution structure determination of membrane proteins.Antigen generation and display in therapeutic antibody drug discovery -- a neglected but critical player.Assembling of the Mycobacterium tuberculosis Cell Wall Core.VirB6 and VirB10 from the Brucella type IV secretion system interact via the N-terminal periplasmic domain of VirB6.Improving heterologous membrane protein production in Escherichia coli by combining transcriptional tuning and codon usage algorithms.Applying bimolecular fluorescence complementation to screen and purify aquaporin protein:protein complexesRestrained expression, a method to overproduce toxic membrane proteins by exploiting operator-repressor interactions.Green Fluorescent Protein as a protein localization and topological reporter in mycobacteria.Optimizing E. coli-Based Membrane Protein Production Using Lemo21(DE3) or pReX and GFP-Fusions.Optimization of Membrane Protein Production Using Titratable Strains of E. coli.Strategies for the production of difficult-to-express full-length eukaryotic proteins using microbial cell factories: production of human alpha-galactosidase A.Substrate-bound outward-open structure of a Na+-coupled sialic acid symporter reveals a new Na+ site.The Sodium Sialic Acid Symporter From Staphylococcus aureus Has Altered Substrate Specificity.
P2860
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P2860
Bridging the gap: a GFP-based strategy for overexpression and purification of membrane proteins with intra and extracellular C-termini.
description
2010 nî lūn-bûn
@nan
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
2010年论文
@zh
2010年论文
@zh-cn
name
Bridging the gap: a GFP-based ...... a and extracellular C-termini.
@en
type
label
Bridging the gap: a GFP-based ...... a and extracellular C-termini.
@en
prefLabel
Bridging the gap: a GFP-based ...... a and extracellular C-termini.
@en
P2093
P2860
P356
P1433
P1476
Bridging the gap: a GFP-based ...... ra and extracellular C-termini
@en
P2093
Gabriel Mercado Besserer
Ha-Quyen Bui
Jeff Abramson
Jennifer M Hsieh
Seunghyug Kwon
P2860
P304
P356
10.1002/PRO.365
P577
2010-04-01T00:00:00Z