Nucleation and propagation of the collagen triple helix in single-chain and trimerized peptides: transition from third to first order kinetics.
暂无分享,去创建一个
R. Kammerer | A. Lustig | J. Engel | J. Stetefeld | T. Schulthess | R. Landwehr | H. Bächinger | Sabine Frank | Richard A Kammerer | Jörg Stetefeld | Therese Schulthess | Ruth Landwehr | Jürgen Engel | Hans Peter Bächinger | Ariel Lustig | Sergei Boudko | S. Boudko | S. Frank
[1] W. Traub,et al. The chemistry and structure of collagen. , 1971, Advances in protein chemistry.
[2] J. Ramshaw,et al. Sequence Dependence of the Folding of Collagen-like Peptides , 1999, The Journal of Biological Chemistry.
[3] R. Berisio,et al. Structural bases of collagen stabilization induced by proline hydroxylation. , 2001, Biopolymers.
[4] C. Geourjon,et al. Trimeric assembly and three-dimensional structure model of the FACIT collagen COL1-NC1 junction from CD and NMR analysis. , 1996, Biochemistry.
[5] V. Mesyanzhinov,et al. The carboxy-terminal domain initiates trimerization of bacteriophage T4 fibritin. , 1999, Biochemistry. Biokhimiia.
[6] R. Raines,et al. Contribution of tertiary amides to the conformational stability of collagen triple helices. , 2001, Biopolymers.
[7] H. Schägger,et al. Tricine-sodium dodecyl sulfate-polyacrylamide gel electrophoresis for the separation of proteins in the range from 1 to 100 kDa. , 1987, Analytical biochemistry.
[8] K. Piez,et al. Equilibrium and kinetic studies of the helix-coil transition in alpha 1-CB2, a small peptide from collagen. , 1970, Biochemistry.
[9] D. Torchia,et al. Detection of cis and trans X-Pro peptide bonds in proteins by 13C NMR: application to collagen. , 1984, Proceedings of the National Academy of Sciences of the United States of America.
[10] J. Engel,et al. The zipper-like folding of collagen triple helices and the effects of mutations that disrupt the zipper. , 1991, Annual review of biophysics and biophysical chemistry.
[11] J. Engel,et al. Folding of collagen IV. , 1988, European journal of biochemistry.
[12] Terry D. Lee,et al. A microscale electrospray interface for on-line, capillary liquid chromatography/tandem mass spectrometry of complex peptide mixtures. , 1995, Analytical chemistry.
[13] L. Castellanos-Serra,et al. Sensitive reverse staining of bacterial lipopolysaccharides on polyacrylamide gels by using zinc and imidazole salts. , 1997, Analytical biochemistry.
[14] Yue Zhang,et al. The Noncollagenous Domain 1 of Type X Collagen , 1999, The Journal of Biological Chemistry.
[15] Y. Sado,et al. Type IV Collagen of the Glomerular Basement Membrane , 2000, The Journal of Biological Chemistry.
[16] M. Eigen,et al. Co-operative non-enzymic base recognition. 3. Kinetics of the helix-coil transition of the oligoribouridylic--oligoriboadenylic acid system and of oligoriboadenylic acid alone at acidic pH. , 1971, Journal of molecular biology.
[17] Y. Itoh,et al. Comparative analysis of the noncollagenous NC1 domain of type IV collagen: Identification of structural features important for assembly, function, and pathogenesis , 1998, Protein science : a publication of the Protein Society.
[18] K. Piez,et al. HELIX FORMATION BY SINGLE- AND DOUBLE-CHAIN GELATINS FROM RAT SKIN COLLAGEN. , 1964, Biochemistry.
[19] J. Engel,et al. Cooperative equilibrium transitions coupled with a slow annealing step explain the sharpness and hysteresis of collagen folding. , 2000, Matrix biology : journal of the International Society for Matrix Biology.
[20] M G Rossmann,et al. Structure of bacteriophage T4 fibritin: a segmented coiled coil and the role of the C-terminal domain. , 1997, Structure.
[21] T. V. Burjanadze,et al. Thermodynamic substantiation of water‐bridged collagen structure , 1992, Biopolymers.
[22] N. Sreerama,et al. Poly(pro)II helices in globular proteins: identification and circular dichroic analysis. , 1994, Biochemistry.
[23] G Fischer,et al. Side-chain effects on peptidyl-prolyl cis/trans isomerisation. , 1998, Journal of molecular biology.
[24] J. Edsall,et al. Physical biochemistry. 2nd ed: By Henry B. Bull, Professor of Chemistry, School of Medicine, Northwestern University, Chicago, Illinois. John Wiley and Sons, New York, N. Y., 1951. viii + 355 pp. Price $5.75 , 1952 .
[25] L. Moroder,et al. Disulfide-Bridged Heterotrimeric Collagen Peptides Containing the Collagenase Cleavage Site of Collagen Type I. Synthesis and Conformational Properties , 1999 .
[26] D. Prockop,et al. Synthesis of (Pro-Hyp-Gly) n of defined molecular weights. Evidence for the stabilization of collagen triple helix by hydroxypyroline. , 1973, Biochimica et biophysica acta.
[27] R. Kammerer,et al. Tenascin-C Hexabrachion Assembly Is a Sequential Two-step Process Initiated by Coiled-coil α-Helices* , 1998, The Journal of Biological Chemistry.
[28] R. Timpl,et al. Three Conformationally Distinct Domains in the Amino-Terminal Segment of Type III Procollagen and Its Rapid Triple Helix ⇄ Coil Transition , 1978 .
[29] D. Reinhardt,et al. Properties of the Collagen Type XVII Ectodomain , 2001, The Journal of Biological Chemistry.
[30] N. Morris,et al. Type IX Collagen NC1 Domain Peptides Can Trimerize in Vitro without Forming a Triple Helix* , 1996, The Journal of Biological Chemistry.
[31] Murray Goodman,et al. A Template-Induced Incipient Collagen-Like Triple-Helical Structure , 1996 .
[32] H M Berman,et al. Crystal and molecular structure of a collagen-like peptide at 1.9 A resolution. , 1994, Science.
[33] H. Bosshard,et al. Folding of a three–stranded coiled coil , 2000, Protein science : a publication of the Protein Society.
[34] R. Timpl,et al. Folding mechanism of the triple helix in type-III collagen and type-III pN-collagen. Role of disulfide bridges and peptide bond isomerization. , 1980, European journal of biochemistry.
[35] R. Kammerer,et al. Stabilization of short collagen-like triple helices by protein engineering. , 2001, Journal of molecular biology.
[36] T. Pihlajaniemi,et al. A short sequence in the N‐terminal region is required for the trimerization of type XIII collagen and is conserved in other collagenous transmembrane proteins , 2000, The EMBO journal.
[37] W. F. Harrington,et al. Collagen structure in solution. I. Kinetics of helix regeneration in single-chain gelatins. , 1970, Biochemistry.
[38] R. Timpl,et al. The Role of Cis-Trans Isomerization of Peptide Bonds in the Coil ⇄ Triple Helix Conversion of Collagen , 1978 .
[39] V. Malashkevich,et al. Crystallization and preliminary crystallographic study of the pentamerizing domain from cartilage oligomeric matrix protein: A five‐stranded α‐helical bundle , 1996 .
[40] J. Engel,et al. The triple helix ⇌ coil conversion of collagen‐like polytripeptides in aqueous and nonaqueous solvents. Comparison of the thermodynamic parameters and the binding of water to (L‐Pro‐L‐Pro‐Gly)n and (L‐Pro‐L‐Hyp‐Gly)n , 1977 .
[41] H. Bächinger,et al. Thermal stability and folding of type IV procollagen and effect of peptidyl-prolyl cis-trans-isomerase on the folding of the triple helix. , 1989, The Journal of biological chemistry.