Cathepsin B carboxydipeptidase specificity analysis using internally quenched fluorescent peptides.
暂无分享,去创建一个
L. Juliano | M. Juliano | A. K. Carmona | Maria Helena S Cezari | Luciano Puzer | Maria Aparecida Juliano | Adriana K Carmona | Luiz Juliano | M. H. Cezari | L. Puzer
[1] A. Barrett,et al. Cathepsin B, Cathepsin H, and cathepsin L. , 1981, Methods in enzymology.
[2] Bonnie F. Sloane,et al. Cathepsin B and human tumor progression. , 1998, Biological chemistry.
[3] R. Ménard,et al. Major increase in endopeptidase activity of human cathepsin B upon removal of occluding loop contacts. , 1997, Biochemistry.
[4] L. Ellerby,et al. Lysosomal Protease Pathways to Apoptosis , 2001, The Journal of Biological Chemistry.
[5] R. Huber,et al. Crystal structure of cathepsin B inhibited with CA030 at 2.0-A resolution: A basis for the design of specific epoxysuccinyl inhibitors. , 1995, Biochemistry.
[6] R Huber,et al. The refined 2.15 A X-ray crystal structure of human liver cathepsin B: the structural basis for its specificity. , 1991, The EMBO journal.
[7] J. Scharfstein,et al. Host Cell Invasion by TRYPANOSOMA cRUZI Is Potentiated by Activation of Bradykinin B2 Receptors , 2000, The Journal of experimental medicine.
[8] D. Buttle,et al. Cathepsin B. , 1997, The international journal of biochemistry & cell biology.
[9] P. Coignet. On specificity , 2003 .
[10] M. Mcgrath. The lysosomal cysteine proteases. , 1999, Annual review of biophysics and biomolecular structure.
[11] J. Scharfstein,et al. Comparison of the specificity, stability and individual rate constants with respective activation parameters for the peptidase activity of cruzipain and its recombinant form, cruzain, from Trypanosoma cruzi. , 2001, European journal of biochemistry.
[12] L. Juliano,et al. Specificity of Cathepsin B to Fluorescent Substrates Containing Benzyl Side-Chain-Substituted Amino Acids at P1 Subsite , 2000, Journal of protein chemistry.
[13] R. Ménard,et al. Engineering of papain: selective alteration of substrate specificity by site-directed mutagenesis. , 1991, Biochemistry.
[14] D. Turk,et al. Revised Definition of Substrate Binding Sites of Papain-Like Cysteine Proteases , 1998, Biological chemistry.
[15] G. H. Coombs,et al. Analysis of the S(2) subsite specificities of the recombinant cysteine proteinases CPB of Leishmania mexicana, and cruzain of Trypanosoma cruzi, using fluorescent substrates containing non-natural basic amino acids. , 2001, Molecular and biochemical parasitology.
[16] T Vernet,et al. Role of the Occluding Loop in Cathepsin B Activity* , 1997, The Journal of Biological Chemistry.
[17] R J Fletterick,et al. Structural determinants of specificity in the cysteine protease cruzain , 1997, Protein science : a publication of the Protein Society.
[18] R. Ménard,et al. Interdependency of sequence and positional specificities for cysteine proteases of the papain family. , 1999, Biochemistry.
[19] R. Ménard,et al. S′2 substrate specificity and the role of His110 and His111 in the exopeptidase activity of human cathepsin B , 2002 .
[20] G. Gores,et al. Cathepsin B contributes to TNF-alpha-mediated hepatocyte apoptosis by promoting mitochondrial release of cytochrome c. , 2000, The Journal of clinical investigation.
[21] C. P. Huber,et al. Crystal structures of recombinant rat cathepsin B and a cathepsin B-inhibitor complex. , 1995, The Journal of Biological Chemistry.
[22] G. Caliendo,et al. Synthesis and hydrolysis by cathepsin B of fluorogenic substrates with the general structure benzoyl-X-ARG-MCA containing non-natural basic amino acids at position X. , 2001, Biochimica et Biophysica Acta.
[23] Bonnie F. Sloane,et al. Molecular regulation, membrane association and secretion of tumor cathepsin B , 1999, APMIS : acta pathologica, microbiologica, et immunologica Scandinavica.
[24] A. Barrett,et al. The specificity of cathepsin B. Hydrolysis of glucagon at the C-terminus by a peptidyldipeptidase mechanism. , 1978, The Biochemical journal.
[25] N. Rawlings,et al. Proteinases 1: lysosomal cysteine proteinases. , 1995, Protein profile.
[26] A. Baici,et al. Stimulation of angiogenesis through cathepsin B inactivation of the tissue inhibitors of matrix metalloproteinases , 1999, FEBS letters.
[27] P. Bonneau,et al. Engineering the S2 subsite specificity of human cathepsin S to a cathepsin L- and cathepsin B-like specificity. , 1994, The Journal of biological chemistry.
[28] Bonnie F. Sloane,et al. Plasma membrane association of cathepsin B in human prostate cancer: Biochemical and immunogold electron microscopic analysis , 2001, The Prostate.
[29] R. Ménard,et al. The specificity of the S1' subsite of cysteine proteases , 1993, FEBS letters.
[30] A. Szpaderska,et al. An intracellular form of cathepsin B contributes to invasiveness in cancer. , 2001, Cancer research.
[31] L. Juliano,et al. Probing the specificity of cysteine proteinases at subsites remote from the active site: analysis of P4, P3, P2' and P3' variations in extended substrates. , 2000, The Biochemical journal.
[32] C. P. Huber,et al. Characterization of cathepsin B specificity by site-directed mutagenesis. Importance of Glu245 in the S2-P2 specificity for arginine and its role in transition state stabilization. , 1993, The Journal of biological chemistry.