Search Results - "Nguyen, Giang K. T"
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Butelase 1 is an Asx-specific ligase enabling peptide macrocyclization and synthesis
Published in Nature chemical biology (01-09-2014)“…Peptide macrocycles are attracting increasing attention as tools for research and as potential therapeutics. The highly efficient butelase 1—homologous to…”
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Total Synthesis of Circular Bacteriocins by Butelase 1
Published in Journal of the American Chemical Society (08-06-2016)“…Circular bacteriocins, ranging from 35 to 70 amino acids, are the largest cyclic peptides produced by lactic acid bacteria to suppress growth of other…”
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3
Characterization and application of natural and recombinant butelase-1 to improve industrial enzymes by end-to-end circularization
Published in RSC advances (30-06-2021)“…Butelase-1, an asparaginyl endopeptidase or legumain, is the prototypical and fastest known Asn/Asp-specific peptide ligase. It is highly useful for…”
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Butelase-mediated synthesis of protein thioesters and its application for tandem chemoenzymatic ligation
Published in Chemical communications (Cambridge, England) (18-12-2015)“…Using a recently discovered peptide ligase, butelase 1, we developed a novel method to access protein thioesters in good yield. We successfully combined it…”
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Engineering a Catalytically Efficient Recombinant Protein Ligase
Published in Journal of the American Chemical Society (19-04-2017)“…Breaking and forming peptidyl bonds are fundamental biochemical reactions in protein chemistry. Unlike proteases that are abundantly available, fast-acting…”
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Butelase-mediated cyclization and ligation of peptides and proteins
Published in Nature protocols (01-10-2016)“…This protocol from Nguyen et al . describes the use of the plant cyclase butelase 1 for the efficient cyclization and ligation of peptides and proteins. After…”
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Butelase-Mediated Macrocyclization of d-Amino-Acid-Containing Peptides
Published in Angewandte Chemie International Edition (04-10-2016)“…Macrocyclic compounds have received increasing attention in recent years. With their large surface area, they hold promise for inhibiting protein–protein…”
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Cyclization of a G4-specific peptide enhances its stability and G-quadruplex binding affinity
Published in Chemical communications (Cambridge, England) (23-01-2020)“…G-quadruplexes (G4) are non-canonical nucleic acid structures with important implications in biology. Based on an α-helical fragment of the RHAU helicase that…”
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Butelase-Mediated Ligation as an Efficient Bioconjugation Method for the Synthesis of Peptide Dendrimers
Published in Bioconjugate chemistry (16-11-2016)“…Herein we report a novel enzymatic bioconjugation method to prepare peptide dendrimers. Under the catalysis of a newly discovered peptide ligase, butelase 1,…”
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Butelase 1: A Versatile Ligase for Peptide and Protein Macrocyclization
Published in Journal of the American Chemical Society (16-12-2015)“…Macrocyclization is a valuable tool for drug design and protein engineering. Although various methods have been developed to prepare macrocycles, a general and…”
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Allotides: Proline-Rich Cystine Knot α‑Amylase Inhibitors from Allamanda cathartica
Published in Journal of natural products (Washington, D.C.) (24-04-2015)“…Cystine knot α-amylase inhibitors belong to a knottin family of peptidyl inhibitors of 30–32 residues and contain two to four prolines. Thus far, only four…”
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Enzymatic Engineering of Live Bacterial Cell Surfaces Using Butelase 1
Published in Angewandte Chemie International Edition (26-06-2017)“…Butelase‐mediated ligation (BML) can be used to modify live bacterial cell surfaces with diverse cargo molecules. Surface‐displayed butelase recognition motif…”
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Site-Specific N-Terminal Labeling of Peptides and Proteins using Butelase 1 and Thiodepsipeptide
Published in Angewandte Chemie International Edition (21-12-2015)“…An efficient ligase with exquisite site‐specificity is highly desirable for protein modification. Recently, we discovered the fastest known ligase called…”
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Orally Active Peptidic Bradykinin B1 Receptor Antagonists Engineered from a Cyclotide Scaffold for Inflammatory Pain Treatment
Published in Angewandte Chemie International Edition (04-06-2012)“…Edible: By grafting natural peptide antagonists onto the cyclotide kalata B1, orally active peptides were engineered, which are potentially useful therapeutics…”
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Ginsentides: Cysteine and Glycine-rich Peptides from the Ginseng Family with Unusual Disulfide Connectivity
Published in Scientific reports (01-11-2018)“…Ginseng, a popular and valuable traditional medicine, has been used for centuries to maintain health and treat disease. Here we report the discovery and…”
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Butelase-Mediated Macrocyclization of d-Amino-Acid-Containing Peptides
Published in Angewandte Chemie (04-10-2016)“…Macrocyclic compounds have received increasing attention in recent years. With their large surface area, they hold promise for inhibiting protein–protein…”
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Identification and Characterization of Roseltide, a Knottin-type Neutrophil Elastase Inhibitor Derived from Hibiscus sabdariffa
Published in Scientific reports (19-12-2016)“…Plant knottins are of therapeutic interest due to their high metabolic stability and inhibitory activity against proteinases involved in human diseases. The…”
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A high-throughput peptidomic strategy to decipher the molecular diversity of cyclic cysteine-rich peptides
Published in Scientific reports (11-03-2016)“…Cyclotides are plant cyclic cysteine-rich peptides (CRPs). The cyclic nature is reported to be gene-determined with a precursor containing a…”
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Site-Specific N-Terminal Labeling of Peptides and Proteins using Butelase 1 and Thiodepsipeptide
Published in Angewandte Chemie (21-12-2015)“…An efficient ligase with exquisite site‐specificity is highly desirable for protein modification. Recently, we discovered the fastest known ligase called…”
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Site-Specific N-Terminal Labeling of Peptides and Proteins using Butelase1 and Thiodepsipeptide
Published in Angewandte Chemie (21-12-2015)“…An efficient ligase with exquisite site-specificity is highly desirable for protein modification. Recently, we discovered the fastest known ligase called…”
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