One-pot three-enzyme chemoenzymatic approach to the synthesis of sialosides containing natural and non-natural functionalities
about
Complete switch from α-2,3- to α-2,6-regioselectivity in Pasteurella dagmatis β-D-galactoside sialyltransferase by active-site redesignCharacterization of Receptor Binding Profiles of Influenza A Viruses Using An Ellipsometry-Based Label-Free Glycan Microarray Assay Platform.Efficient chemoenzymatic synthesis of biotinylated human serum albumin-sialoglycoside conjugates containing O-acetylated sialic acids.Improving low-temperature activity of Sulfolobus acidocaldarius 2-keto-3-deoxygluconate aldolase.Advances in the biology and chemistry of sialic acids.Chemoenzymatic synthesis of GD3 oligosaccharides and other disialyl glycans containing natural and non-natural sialic acidsNovel anti-Sialyl-Tn monoclonal antibodies and antibody-drug conjugates demonstrate tumor specificity and anti-tumor activity.Chemoenzymatic synthesis of α2-3-sialylated carbohydrate epitopes.Enzymatic route to preparative-scale synthesis of UDP-GlcNAc/GalNAc, their analogues and GDP-fucoseChemoenzymatic synthesis of the sialyl Lewis X glycan and its derivatives.Exploration of sialic acid diversity and biology using sialoglycan microarrays.Human xeno-autoantibodies against a non-human sialic acid serve as novel serum biomarkers and immunotherapeutics in cancer.Chemoenzymatic synthesis of sialosides containing C7-modified sialic acids and their application in sialidase substrate specificity studies.Chemoenzymatic synthesis of C8-modified sialic acids and related α2-3- and α2-6-linked sialosides.A sialylated glycan microarray reveals novel interactions of modified sialic acids with proteins and viruses.Protein glycoengineering enabled by the versatile synthesis of aminooxy glycans and the genetically encoded aldehyde tagCross-comparison of protein recognition of sialic acid diversity on two novel sialoglycan microarrays.Converting Pasteurella multocidaα2-3-sialyltransferase 1 (PmST1) to a regioselective α2-6-sialyltransferase by saturation mutagenesis and regioselective screening.Sialic acid metabolism and sialyltransferases: natural functions and applications.Enhanced Cross-Linking of Diazirine-Modified Sialylated Glycoproteins Enabled through Profiling of Sialidase Specificities.Structural Basis for Sialoglycan Binding by the Streptococcus sanguinis SrpA Adhesin.Controlled Multi-functionalization Facilitates Targeted Delivery of Nanoparticles to Cancer Cells.Diversity in specificity, abundance, and composition of anti-Neu5Gc antibodies in normal humans: potential implications for diseaseParallel chemoenzymatic synthesis of sialosides containing a C5-diversified sialic acidSynthetic antigens reveal dynamics of BCR endocytosis during inhibitory signalingRecent advances in chemoenzymatic peptide syntheses.Chemoenzymatic Syntheses of Sialylated Oligosaccharides Containing C5-Modified Neuraminic Acids for Dual Inhibition of Hemagglutinins and Neuraminidases.Cloning and characterization of a viral α2-3-sialyltransferase (vST3Gal-I) for the synthesis of sialyl Lewisx.Enzymatic synthesis of lactosylated and sialylated derivatives of epothilone A.Glycosyltransferase engineering for carbohydrate synthesis.Efficient chemoenzymatic synthesis of sialyl Tn-antigens and derivatives.One-pot multienzyme (OPME) systems for chemoenzymatic synthesis of carbohydrates.Disubstituted Sialic Acid Ligands Targeting Siglecs CD33 and CD22 Associated with Myeloid Leukaemias and B Cell Lymphomas.A Chemical Biology Solution to Problems with Studying Biologically Important but Unstable 9-O-Acetyl Sialic Acids.Effective one-pot multienzyme (OPME) synthesis of monotreme milk oligosaccharides and other sialosides containing 4-O-acetyl sialic acid.Sequential one-pot multienzyme (OPME) synthesis of lacto-N-neotetraose and its sialyl and fucosyl derivatives.One-pot multienzyme synthesis of Lewis x and sialyl Lewis x antigens.Combinatorial chemoenzymatic synthesis and high-throughput screening of sialosides.Chemical preparation of sialyl Lewis x using an enzymatically synthesized sialoside building block.Systematic Chemoenzymatic Synthesis of O-Sulfated Sialyl Lewis x Antigens
P2860
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P2860
One-pot three-enzyme chemoenzymatic approach to the synthesis of sialosides containing natural and non-natural functionalities
description
2006 nî lūn-bûn
@nan
2006 թուականին հրատարակուած գիտական յօդուած
@hyw
2006 թվականին հրատարակված գիտական հոդված
@hy
2006年の論文
@ja
2006年論文
@yue
2006年論文
@zh-hant
2006年論文
@zh-hk
2006年論文
@zh-mo
2006年論文
@zh-tw
2006年论文
@wuu
name
One-pot three-enzyme chemoenzy ...... nd non-natural functionalities
@ast
One-pot three-enzyme chemoenzy ...... nd non-natural functionalities
@en
One-pot three-enzyme chemoenzy ...... nd non-natural functionalities
@nl
type
label
One-pot three-enzyme chemoenzy ...... nd non-natural functionalities
@ast
One-pot three-enzyme chemoenzy ...... nd non-natural functionalities
@en
One-pot three-enzyme chemoenzy ...... nd non-natural functionalities
@nl
prefLabel
One-pot three-enzyme chemoenzy ...... nd non-natural functionalities
@ast
One-pot three-enzyme chemoenzy ...... nd non-natural functionalities
@en
One-pot three-enzyme chemoenzy ...... nd non-natural functionalities
@nl
P2093
P2860
P356
P1433
P1476
One-pot three-enzyme chemoenzy ...... nd non-natural functionalities
@en
P2093
Harshal A Chokhawala
Shengshu Huang
P2860
P2888
P304
P356
10.1038/NPROT.2006.401
P407
P577
2006-01-01T00:00:00Z
P5875
P6179
1000208223