The biochemical properties of α-1,3-galactosyltransferase WciN from serotype 6B were systemically characterized with the chemically synthesized Glcα-PP-(CH)-OPh as an acceptor substrate. The site-directed mutation of D38 and A150 residues of WciN was further investigated, and the enzymatic activities of those WciN mutants revealed that A150 residue was the pivotal residue responsible for nucleotide donor recognition and the single-site mutation could completely cause pneumococcus serotype switch. Using WciN and WciN mutants as useful tool enzymes, the disaccharides Galα1,3Glcα-PP-(CH)-OPh and Glcα1,3Glcα-PP-(CH)-OPh were successfully prepared in multi-milligram scale in high yields.
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http://dx.doi.org/10.3389/fchem.2022.914698 | DOI Listing |
Transl Lung Cancer Res
April 2024
Department of Thoracic Oncology and Surgery, China State Key Laboratory of Respiratory Disease & National Clinical Research Center for Respiratory Disease, the First Affiliated Hospital of Guangzhou Medical University, Guangzhou, China.
Background: Albeit considered with superior survival, around 30% of the early-stage non-squamous non-small cell lung cancer (Ns-NSCLC) patients relapse within 5 years, suggesting unique biology. However, the biological characteristics of early-stage Ns-NSCLC, especially in the Chinese population, are still unclear.
Methods: Multi-omics interrogation of early-stage Ns-NSCLC (stage I-III), paired blood samples and normal lung tissues (n=76) by whole-exome sequencing (WES), RNA sequencing, and T-cell receptor (TCR) sequencing were conducted.
Nat Commun
September 2023
Oxford Motor Neuron Disease Centre, Nuffield Department of Clinical Neurosciences, University of Oxford, John Radcliffe Hospital, Oxford, OX3 9DU, UK.
Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disease characterized by progressive motor neuron loss, with additional pathophysiological involvement of non-neuronal cells such as microglia. The commonest ALS-associated genetic variant is a hexanucleotide repeat expansion (HRE) mutation in C9orf72. Here, we study its consequences for microglial function using human iPSC-derived microglia.
View Article and Find Full Text PDFFront Chem
June 2022
National Glycoengineering Research Center, Shandong Provincial Key Laboratory of Carbohydrate Chemistry and Glycobiology, Shandong University, Qingdao, China.
The biochemical properties of α-1,3-galactosyltransferase WciN from serotype 6B were systemically characterized with the chemically synthesized Glcα-PP-(CH)-OPh as an acceptor substrate. The site-directed mutation of D38 and A150 residues of WciN was further investigated, and the enzymatic activities of those WciN mutants revealed that A150 residue was the pivotal residue responsible for nucleotide donor recognition and the single-site mutation could completely cause pneumococcus serotype switch. Using WciN and WciN mutants as useful tool enzymes, the disaccharides Galα1,3Glcα-PP-(CH)-OPh and Glcα1,3Glcα-PP-(CH)-OPh were successfully prepared in multi-milligram scale in high yields.
View Article and Find Full Text PDFAm J Hum Genet
June 2016
Institute of Human Genetics, Technische Universität München, 81675 Munich, Germany; Institute of Human Genetics, Helmholtz Zentrum München, 85764 Neuherberg, Germany.
Multiple acyl-CoA dehydrogenase deficiencies (MADDs) are a heterogeneous group of metabolic disorders with combined respiratory-chain deficiency and a neuromuscular phenotype. Despite recent advances in understanding the genetic basis of MADD, a number of cases remain unexplained. Here, we report clinically relevant variants in FLAD1, which encodes FAD synthase (FADS), as the cause of MADD and respiratory-chain dysfunction in nine individuals recruited from metabolic centers in six countries.
View Article and Find Full Text PDFBiochemistry
July 2012
State Key Laboratory of Medicinal Chemical Biology, Nankai University, Tianjin 300071, China.
Almost all Streptococcus pneumoniae (pneumococcus) capsule serotypes employ the Wzy-dependent pathway for their capsular polysaccharide (CPS) biosynthesis. The assembly of the CPS repeating unit (RU) is the first committed step in this pathway. The wciN gene was predicted to encode a galactosyltransferase involved in the RU assembly of pneumococcus type 6B CPS.
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