BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

1086 related articles for article (PubMed ID: 8573578)

  • 1. Thermodynamics of the membrane insertion process of the M13 procoat protein, a lipid bilayer traversing protein containing a leader sequence.
    Soekarjo M; Eisenhawer M; Kuhn A; Vogel H
    Biochemistry; 1996 Jan; 35(4):1232-41. PubMed ID: 8573578
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Protein transduction domains of HIV-1 and SIV TAT interact with charged lipid vesicles. Binding mechanism and thermodynamic analysis.
    Ziegler A; Blatter XL; Seelig A; Seelig J
    Biochemistry; 2003 Aug; 42(30):9185-94. PubMed ID: 12885253
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Cysteine residues in the transmembrane regions of M13 procoat protein suggest that oligomeric coat proteins assemble onto phage progeny.
    Nagler C; Nagler G; Kuhn A
    J Bacteriol; 2007 Apr; 189(7):2897-905. PubMed ID: 17237167
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The activation energy for insertion of transmembrane alpha-helices is dependent on membrane composition.
    Meijberg W; Booth PJ
    J Mol Biol; 2002 Jun; 319(3):839-53. PubMed ID: 12054874
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Mimicking initial interactions of bacteriophage M13 coat protein disassembly in model membrane systems.
    Stopar D; Spruijt RB; Wolfs CJ; Hemminga MA
    Biochemistry; 1998 Jul; 37(28):10181-7. PubMed ID: 9665724
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Fluorescence resonance energy transfer shows a close helix-helix distance in the transmembrane M13 procoat protein.
    Eisenhawer M; Cattarinussi S; Kuhn A; Vogel H
    Biochemistry; 2001 Oct; 40(41):12321-8. PubMed ID: 11591151
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Magainin 2 amide interaction with lipid membranes: calorimetric detection of peptide binding and pore formation.
    Wenk MR; Seelig J
    Biochemistry; 1998 Mar; 37(11):3909-16. PubMed ID: 9521712
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Modulation of the binding of signal peptides to lipid bilayers by dipoles near the hydrocarbon-water interface.
    Voglino L; McIntosh TJ; Simon SA
    Biochemistry; 1998 Sep; 37(35):12241-52. PubMed ID: 9724538
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Membrane assembly of M13 major coat protein: evidence for a structural adaptation in the hinge region and a tilted transmembrane domain.
    Spruijt RB; Wolfs CJ; Hemminga MA
    Biochemistry; 2004 Nov; 43(44):13972-80. PubMed ID: 15518546
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Mode of insertion of the signal sequence of a bacterial precursor protein into phospholipid bilayers as revealed by cysteine-based site-directed spectroscopy.
    Keller RC; ten Berge D; Nouwen N; Snel MM; Tommassen J; Marsh D; de Kruijff B
    Biochemistry; 1996 Mar; 35(9):3063-71. PubMed ID: 8608147
    [TBL] [Abstract][Full Text] [Related]  

  • 11. The cytoplasmic carboxy terminus of M13 procoat is required for the membrane insertion of its central domain.
    Kuhn A; Wickner W; Kreil G
    Nature; 1986 Jul 24-30; 322(6077):335-9. PubMed ID: 3526160
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Structural characterization of membrane insertion of M13 procoat, M13 coat, and Pf3 coat proteins.
    Thiaudière E; Soekarjo M; Kuchinka E; Kuhn A; Vogel H
    Biochemistry; 1993 Nov; 32(45):12186-96. PubMed ID: 8218296
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Binding of antibacterial magainin peptides to electrically neutral membranes: thermodynamics and structure.
    Wieprecht T; Beyermann M; Seelig J
    Biochemistry; 1999 Aug; 38(32):10377-87. PubMed ID: 10441132
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Binding of oligoarginine to membrane lipids and heparan sulfate: structural and thermodynamic characterization of a cell-penetrating peptide.
    Gonçalves E; Kitas E; Seelig J
    Biochemistry; 2005 Feb; 44(7):2692-702. PubMed ID: 15709783
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Bacteriophage M13 procoat protein inserts into the plasma membrane as a loop structure.
    Kuhn A
    Science; 1987 Dec; 238(4832):1413-5. PubMed ID: 3317833
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Orientation of LamB signal peptides in bilayers: influence of lipid probes on peptide binding and interpretation of fluorescence quenching data.
    Voglino L; Simon SA; McIntosh TJ
    Biochemistry; 1999 Jun; 38(23):7509-16. PubMed ID: 10360948
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Conditional lethal mutations separate the M13 procoat and Pf3 coat functions of YidC: different YIDC structural requirements for membrane protein insertion.
    Chen M; Xie K; Nouwen N; Driessen AJ; Dalbey RE
    J Biol Chem; 2003 Jun; 278(26):23295-300. PubMed ID: 12707259
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Octyl-beta-D-glucopyranoside partitioning into lipid bilayers: thermodynamics of binding and structural changes of the bilayer.
    Wenk MR; Alt T; Seelig A; Seelig J
    Biophys J; 1997 Apr; 72(4):1719-31. PubMed ID: 9083676
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Local dynamics of the M13 major coat protein in different membrane-mimicking systems.
    Stopar D; Spruijt RB; Wolfs CJ; Hemminga MA
    Biochemistry; 1996 Dec; 35(48):15467-73. PubMed ID: 8952500
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Conformational and aggregational properties of the gene 9 minor coat protein of bacteriophage M13 in membrane-mimicking systems.
    Houbiers MC; Spruijt RB; Wolfs CJ; Hemminga MA
    Biochemistry; 1999 Jan; 38(3):1128-35. PubMed ID: 9894010
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 55.