How the molecular weight affects the in vivo fate of exogenous hyaluronan delivered intravenously: A stable-isotope labelling strategy

2021 ◽  
Vol 263 ◽  
pp. 117927
Author(s):  
Matěj Šimek ◽  
Kristina Nešporová ◽  
Anna Kocurková ◽  
Tereza Foglová ◽  
Gabriela Ambrožová ◽  
...  
PROTEOMICS ◽  
2002 ◽  
Vol 2 (2) ◽  
pp. 157-163 ◽  
Author(s):  
Julie M. Pratt ◽  
Duncan H. L. Robertson ◽  
Simon J. Gaskell ◽  
Isabel Riba-Garcia ◽  
Simon J. Hubbard ◽  
...  

2019 ◽  
Author(s):  
Ser Sue Ng ◽  
Jung Eun Park ◽  
Wei Meng ◽  
Christopher Li-Hsian Chen ◽  
Raj N. Kalaria ◽  
...  

AbstractIdentification of proteins that are synthesized de novo in response to specific microenvironmental cues is critical to understanding the molecular mechanisms that underpin key physiological processes and pathologies. Here we report that a brief period of pulsed SILAC diet (Stable Isotope Labelling by Amino acids in Cell culture) enables determination of biological functions corresponding to actively translating proteins in the mouse brain. Our data demonstrate that the hippocampus, cortex and cerebellum are highly active sites of protein synthesis, rapidly expressing key mediators of nutrient sensing and lipid metabolism, as well as critical regulators of synaptic function, axon guidance, and circadian entrainment. Together, these findings confirm that protein metabolic activity varies significantly between brain regions in vivo and indicate that pSILAC-based approaches can identify specific anatomical sites and biological pathways likely to be suitable for drug targeting in neurodegenerative disorders.AbbreviationsApoA1: Apolipoprotein A1, ApoA4: Apolipoprotein A4, ApoE: Apolipoprotein E, ApoJ/Clu: Apolipoprotein J/Clusterin, App: Amyloid-β precursor/A4 protein: App, HDL: high density lipoprotein, Lrp1: Low density lipoprotein receptor-related protein 1, pSILAC: pulsed SILAC, pSIVOM: pulsed-SILAC in vivo labelling in mouse, SILAC: Stable Isotope Labelling by Amino acids in Cell culture)


2010 ◽  
Vol 95 (Suppl 1) ◽  
pp. A43.1-A43
Author(s):  
K Goss ◽  
L Ward ◽  
V Ledger ◽  
G Koster ◽  
P Townsend ◽  
...  

2019 ◽  
Vol 14 (2) ◽  
pp. 313-330 ◽  
Author(s):  
Min Yuan ◽  
Daniel M. Kremer ◽  
He Huang ◽  
Susanne B. Breitkopf ◽  
Issam Ben-Sahra ◽  
...  

2017 ◽  
Vol 4 (3) ◽  
pp. 160810 ◽  
Author(s):  
Elena Gorokhova

In ecology, stable isotope labelling is commonly used for tracing material transfer in trophic interactions, nutrient budgets and biogeochemical processes. The main assumption in this approach is that the enrichment with a heavy isotope has no effect on the organism growth and metabolism. This assumption is, however, challenged by theoretical considerations and experimental studies on kinetic isotope effects in vivo . Here, I demonstrate profound changes in life histories of the rotifer Brachionus plicatilis fed 15 N-enriched algae (0.4–5.0 at%); i.e. at the enrichment levels commonly used in ecological studies. These findings support theoretically predicted effects of heavy isotope enrichment on growth, metabolism and ageing in biological systems and underline the importance of accounting for such effects when using stable isotope labelling in experimental studies.


2009 ◽  
Vol 877 (26) ◽  
pp. 2716-2721 ◽  
Author(s):  
Anthony D. Postle ◽  
Alan N. Hunt

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