[HTML][HTML] Mucus sialylation determines intestinal host-commensal homeostasis

Y Yao, G Kim, S Shafer, Z Chen, S Kubo, Y Ji, J Luo… - Cell, 2022 - cell.com
Intestinal mucus forms the first line of defense against bacterial invasion while providing
nutrition to support microbial symbiosis. How the host controls mucus barrier integrity and …

Parameter reliability and understanding enzyme function

AG McDonald, KF Tipton - Molecules, 2022 - mdpi.com
Knowledge of the Michaelis–Menten parameters and their meaning in different
circumstances is an essential prerequisite to understanding enzyme function and behaviour …

Analysis of carbohydrates and glycoconjugates by matrix‐assisted laser desorption/ionization mass spectrometry: An update for 2019–2020

DJ Harvey - Mass Spectrometry Reviews, 2023 - Wiley Online Library
This review is the tenth update of the original article published in 1999 on the application of
matrix‐assisted laser desorption/ionization (MALDI) mass spectrometry to the analysis of …

Delivery of nucleotide sugars to the mammalian Golgi: a very well (un) explained story

D Maszczak-Seneczko, M Wiktor, E Skurska… - International Journal of …, 2022 - mdpi.com
Nucleotide sugars (NSs) serve as substrates for glycosylation reactions. The majority of
these compounds are synthesized in the cytoplasm, whereas glycosylation occurs in the …

B4GALT1 as a new biomarker of idiopathic pulmonary fibrosis

C De Vitis, M D'Ascanio, A Sacconi… - International Journal of …, 2022 - mdpi.com
Idiopathic pulmonary fibrosis (IPF) is a disease characterized by progressive scarring of the
lung that involves the pulmonary interstitium. The disease may rapidly progress, leading to …

SLC35A2 Deficiency Promotes an Epithelial-to-Mesenchymal Transition-like Phenotype in Madin–Darby Canine Kidney Cells

M Kot, E Mazurkiewicz, M Wiktor, W Wiertelak… - Cells, 2022 - mdpi.com
In mammalian cells, SLC35A2 delivers UDP–galactose for galactosylation reactions that
take place predominantly in the Golgi lumen. Mutations in the corresponding gene cause a …

Novel Insights into Selected Disease-Causing Mutations within the SLC35A1 Gene Encoding the CMP-Sialic Acid Transporter

B Szulc, Y Zadorozhna, M Olczak, W Wiertelak… - International Journal of …, 2020 - mdpi.com
Congenital disorders of glycosylation (CDG) are a group of rare genetic and metabolic
diseases caused by alterations in glycosylation pathways. Five patients bearing CDG …

The critical role of B4GALT4 in promoting microtubule spindle assembly in HCC through the regulation of PLK1 and RHAMM expression

Z Dai, K Wang, Y Gao - Journal of Cellular Physiology, 2022 - Wiley Online Library
Abstract Beta 1, 4‐galactosyltransferase (B4GALT)‐family glycosyltransferases are involved
in multiple biological processes promoting cancer progression, regulating the dynamic …

[HTML][HTML] An interaction between SLC35A1 and ST3Gal4 is differentially affected by CDG-causing mutations in the SLC35A1 gene

W Wiertelak, M Olczak… - … and Biophysical Research …, 2022 - Elsevier
The sialylation of glycoconjugates is performed by a variety of sialyltransferases using CMP-
sialic acid (CMP-Sia) as a substrate. Sialylation requires the translocation of CMP-Sia …

[HTML][HTML] SLC35A2 deficiency reduces protein levels of core 1 β-1, 3-galactosyltransferase 1 (C1GalT1) and its chaperone Cosmc and affects their subcellular …

W Wiertelak, K Chabowska, B Szulc… - … et Biophysica Acta (BBA …, 2023 - Elsevier
Nucleotide sugar transporters (NSTs) are multitransmembrane proteins, localized in the
Golgi apparatus and/or endoplasmic reticulum, which provide glycosylation enzymes with …