Studies on chymotrypsin-like catalysis by synthetic peptides
@article{Corey1994StudiesOC, title={Studies on chymotrypsin-like catalysis by synthetic peptides}, author={Michael J. Corey and Eva Hallakova and Kathleen C. Pugh and John M Stewart}, journal={Applied Biochemistry and Biotechnology}, year={1994}, volume={47}, pages={199-212} }
The synthetic peptide Chymohelizyme-1 (CHZ-1) exhibits esterase activity against carbobenzoxytyrosinep-nitrophenyl ester (ZTONP), carbobenzoxyalaninep-nitrophenyl ester (ZAONP), andt-butyloxycarbonyltyrosinep-nitrophenyl ester (BocTONP). However, earlier reports of catalytic activity against less labile esters and amides have proven to be incorrect. The major reason for the errors appears to have been the omission of certain controls in the previous work. Although the catalytic triad does not…
14 Citations
Design, synthesis and catalytic activity of a serine protease synthetic model
- Chemistry, BiologyLetters in Peptide Science
- 2006
Results suggest that the designed carrier brings in appropriate contact the catalytic triad residues (Ser, His, Asp) resulting in the obtained hydrolytic activity.
De novo designed polypeptide catalysts with adopted folded structures
- Chemistry, Biology
- 1998
It was found that so far the most severe limitation of folded polypeptide catalysts is the efficiency obtained in the bond-making and bond-breaking steps, whereas the binding of substrates, even on the surface of helical structures in aqueous solution, is of comparable strength to that which occurs in nature.
Polypeptides with supersecondary structures as templates in rational catalyst design. Catalysis of self functionalization by designed helix–loop–helix motifs
- Chemistry, Biology
- 1996
The ability of a designed helix–loop–helix motif, RA-42, to catalyse its own functionalization is thereby demonstrated for the first time.
Interhelical carbon bridging of catalytic helix–loop–helix polypeptide motifs
- Chemistry, Biology
- 2000
The catalysis of the site-selective reaction has been investigated in detail using a number of designed helix–loop–helix polypeptide motifs that have been reacted with DSG and the longer N-hydroxysuccinimide ester bis(sulfosucc inimidyl) suberate (BS3).
Structure of a cyclic peptide with a catalytic triad, determined by computer simulation and NMR spectroscopy
- Biology, ChemistryJ. Comput. Aided Mol. Des.
- 1996
A cyclic, eight-residue peptide that possesses the catalytic triad residues of the serine proteases is reported that is synthesised and purified and hydrolyses p-nitrophenyl acetate about nine times faster than free histidine.
Site-selective control of the reactivity of surface-exposed histidine residues in designed four-helix-bundle catalysts.
- BiologyFolding & design
- 1998
Synthesis of functionalised nucleosides for incorporation into nucleic acid-based serine protease mimics.
- Chemistry, BiologyMolecules
- 2007
The synthesis of nucleosides modified with an extra imidazole, carboxyl and hydroxyl group can be incorporated into an oligonucleotide duplex, thus generating a novel type of serine protease mimic.
Functionalization and Properties of Designed Folded Polypeptides
- Biology, Chemistry
- 1999
Strategies for functionalization using both the naturally occurring amino acids and post-synthetic incorporation of non-natural functionality will be described, as well as the level of function that has been achieved by rational design.
Protein Design: A Hierarchic Approach
- BiologyScience
- 1995
The de novo design of peptides and proteins has recently emerged as an approach for investigating protein structure and function. Designed, helical peptides provide model systems for dissecting and…
References
SHOWING 1-7 OF 7 REFERENCES
Design and synthesis of a peptide having chymotrypsin-like esterase activity.
- Biology, ChemistryScience
- 1990
A peptide having enzyme-like catalytic activity has been designed and synthesized and is inhibited by ChTr specific inhibitors and is inactive toward benzoyl arginine ethyl ester, a trypsin substrate.
An NADH-coupled assay for femtogram or nanogram quantities of chymotrypsin.
- Biology, ChemistryAnalytical biochemistry
- 1983
Synthesis and stability of 3-nitro-2-pyridinesulfenyl chloride (NpysCl).
- ChemistryInternational journal of peptide and protein research
- 1993
The stability of NpysCl was determined in a variety of solvents, with and without base, to determine the most suitable solvent and base for the synthesis of N-Npys amino acids.
The binding of nucleotides by pancreatic ribonuclease. I. Proton uptake and release associated with anion binding.
- Biology, ChemistryThe Journal of biological chemistry
- 1966
Interactions involving both electrostatic and hydrogen bonding between the phosphate group and the binding site appear to explain the considerable stability of RNase-nucleotide complexes, and changes in the H+ concentration caused by the addition of various competitive inhibitors at the same pH.
Solid Phase Peptide Synthesis
- Chemistry, Biology
- 1984
This work has shown that effective methods of peptide synthesis are crucial to progress in this area, because only by synthesis can adequate amounts of important peptides be made available for chemical, biologi...
Effects of resin swelling and substitution on solid phase synthesis.
- Chemistry, Materials ScienceInternational journal of peptide and protein research
- 1992
Effects of resin swelling, uniformity, and substitution on the solid phase synthesis of long, structured and/or branched peptides were evaluated.