Hydrogel Viscoelasticity Modulates Cell Nascent Extracellular Matrix Deposition
In this study, interpenetrating polymer network hydrogels with tunable viscoelastic properties were developed to study the mechanical regulation of nascent extracellular matrix (nECM) deposition. Cells cultured on high‐viscosity (high tanδ) hydrogels deposited more nECM and increased hydrogel remodeling independent of cellular contraction forces. These
Matthew L. Tan +5 more
wiley +1 more source
Activating pyruvate kinase improves red blood cell integrity by reducing band 3 tyrosine phosphorylation. [PDF]
Le K +13 more
europepmc +1 more source
Mass Spectrometry Structural Proteomics Enabled by Limited Proteolysis and Cross‐Linking
ABSTRACT The exploration of protein structure and function stands at the forefront of life science and represents an ever‐expanding focus in the development of proteomics. As mass spectrometry (MS) offers readout of protein conformational changes at both the protein and peptide levels, MS‐based structural proteomics is making significant strides in the
Haiyan Lu +4 more
wiley +1 more source
Pyruvate Kinase M1/2 Proteoformics for Accurate Insights into Energy Metabolism Abnormity to Promote the Overall Management of Ovarian Cancer Towards Predictive, Preventive, and Personalized Medicine Approaches. [PDF]
Wang Y +4 more
europepmc +1 more source
Interactions of tumor necrosis factor receptor-associated factor 4 and pyruvate kinase muscle isoform 2 promote malignant behavior and aerobic glycolysis in colorectal cancer cells. [PDF]
Liu T, Zhu S, Sun J, Ma Y.
europepmc +1 more source
Pyruvate Kinase M2-Responsive Release of Paclitaxel and Indoleamine 2,3-Dioxygenase Inhibitor for Immuno-Chemotherapy of Nonsmall Cell Lung Cancer. [PDF]
Wu H +13 more
europepmc +1 more source
Hydrogen sulfide coordinates glucose metabolism switch through destabilizing tetrameric pyruvate kinase M2. [PDF]
Wang RH +20 more
europepmc +1 more source
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Pyruvate kinase (PK) deficiency due to mutations of the PKLR gene is a common cause of hereditary nonspherocytic hemolytic anemia. Thus far, 55 different mutations have been described in patients with PK-deficient hemolytic anemia. Polymorphisms within the PKLR gene and in the tightly linked glucocerebrosidase (GBA) gene suggest that PK deficiency may ...
Ernest Beutler, Luciano Baronciani
openaire +3 more sources

