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154 related items for PubMed ID: 20454718
1. Quantitative determination of protein stability and ligand binding using a green fluorescent protein reporter system. Moreau MJ, Morin I, Schaeffer PM. Mol Biosyst; 2010 Jul; 6(7):1285-92. PubMed ID: 20454718 [Abstract] [Full Text] [Related]
2. Enhancing the stability and solubility of the glucocorticoid receptor ligand-binding domain by high-throughput library screening. Seitz T, Thoma R, Schoch GA, Stihle M, Benz J, D'Arcy B, Wiget A, Ruf A, Hennig M, Sterner R. J Mol Biol; 2010 Nov 05; 403(4):562-77. PubMed ID: 20850457 [Abstract] [Full Text] [Related]
3. Assessment of membrane protein expression and stability using a split green fluorescent protein reporter. Rodríguez-Banqueri A, Kowalczyk L, Palacín M, Vázquez-Ibar JL. Anal Biochem; 2012 Apr 01; 423(1):7-14. PubMed ID: 22285978 [Abstract] [Full Text] [Related]
4. Development of a protease activity assay using heat-sensitive Tus-GFP fusion protein substrates. Askin SP, Morin I, Schaeffer PM. Anal Biochem; 2011 Aug 15; 415(2):126-33. PubMed ID: 21570945 [Abstract] [Full Text] [Related]
5. Thermodynamic analysis of ligand-induced changes in protein thermal unfolding applied to high-throughput determination of ligand affinities with extrinsic fluorescent dyes. Layton CJ, Hellinga HW. Biochemistry; 2010 Dec 28; 49(51):10831-41. PubMed ID: 21050007 [Abstract] [Full Text] [Related]
6. How disorder influences order and vice versa--mutual effects in fusion proteins containing an intrinsically disordered and a globular protein. Sambi I, Gatti-Lafranconi P, Longhi S, Lotti M. FEBS J; 2010 Nov 28; 277(21):4438-51. PubMed ID: 20875082 [Abstract] [Full Text] [Related]
7. Efficient selection of IgG Fc domain-binding peptides fused to fluorescent protein using E. coli expression system and dot-blotting assay. Jeong YJ, Kang HJ, Bae KH, Kim MG, Chung SJ. Peptides; 2010 Feb 28; 31(2):202-6. PubMed ID: 20025916 [Abstract] [Full Text] [Related]
8. Green fluorescent protein-tagging reduces the nucleocytoplasmic shuttling specifically of unphosphorylated STAT1. Meyer T, Begitt A, Vinkemeier U. FEBS J; 2007 Feb 28; 274(3):815-26. PubMed ID: 17288561 [Abstract] [Full Text] [Related]
9. A general technique to rank protein-ligand binding affinities and determine allosteric versus direct binding site competition in compound mixtures. Annis DA, Nazef N, Chuang CC, Scott MP, Nash HM. J Am Chem Soc; 2004 Dec 01; 126(47):15495-503. PubMed ID: 15563178 [Abstract] [Full Text] [Related]
10. A simple dual selection for functionally active mutants of Plasmodium falciparum dihydrofolate reductase with improved solubility. Japrung D, Chusacultanachai S, Yuvaniyama J, Wilairat P, Yuthavong Y. Protein Eng Des Sel; 2005 Oct 01; 18(10):457-64. PubMed ID: 16120637 [Abstract] [Full Text] [Related]
11. Temperature influence on fluorescence intensity and enzyme activity of the fusion protein of GFP and hyperthermophilic xylanase. Zhang C, Liu MS, Xing XH. Appl Microbiol Biotechnol; 2009 Sep 01; 84(3):511-7. PubMed ID: 19390851 [Abstract] [Full Text] [Related]
12. Green fluorescent protein as a reporter for macromolecular localization in bacterial cells. Margolin W. Methods; 2000 Jan 01; 20(1):62-72. PubMed ID: 10610805 [Abstract] [Full Text] [Related]
13. Comparative analysis of protein aggregates by blue native electrophoresis and subsequent sodium dodecyl sulfate-polyacrylamide gel electrophoresis in a three-dimensional geometry gel. Stegemann J, Ventzki R, Schrödel A, de Marco A. Proteomics; 2005 May 01; 5(8):2002-9. PubMed ID: 15841497 [Abstract] [Full Text] [Related]
14. Investigation of charged polymer influence on green fluorescent protein thermal stability. de Lencastre Novaes LC, Mazzola PG, Pessoa A, Vessoni Penna TC. N Biotechnol; 2011 Jul 01; 28(4):391-5. PubMed ID: 21334469 [Abstract] [Full Text] [Related]
15. Pulse proteolysis: a simple method for quantitative determination of protein stability and ligand binding. Park C, Marqusee S. Nat Methods; 2005 Mar 01; 2(3):207-12. PubMed ID: 15782190 [Abstract] [Full Text] [Related]
17. Green fluorescent protein and factorial approach: an effective partnership for screening the soluble expression of recombinant proteins in Escherichia coli. Coutard B, Gagnaire M, Guilhon AA, Berro M, Canaan S, Bignon C. Protein Expr Purif; 2008 Oct 01; 61(2):184-90. PubMed ID: 18602837 [Abstract] [Full Text] [Related]
19. Observations of green fluorescent protein as a fusion partner in genetically engineered Escherichia coli: monitoring protein expression and solubility. Cha HJ, Wu CF, Valdes JJ, Rao G, Bentley WE. Biotechnol Bioeng; 2000 Mar 05; 67(5):565-74. PubMed ID: 10649231 [Abstract] [Full Text] [Related]