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Salt Potentiates Methylamine Counteraction System to Offset the Deleterious Effects of Urea on Protein Stability and Function
- Source :
- PLoS ONE, PLoS ONE, Vol 10, Iss 3, p e0119597 (2015)
- Publication Year :
- 2015
- Publisher :
- Public Library of Science (PLoS), 2015.
-
Abstract
- Cellular methylamines are osmolytes (low molecular weight organic compounds) believed to offset the urea's harmful effects on the stability and function of proteins in mammalian kidney and marine invertebrates. Although urea and methylamines are found at 2:1 molar ratio in tissues, their opposing effects on protein structure and function have been questioned on several grounds including failure to counteraction or partial counteraction. Here we investigated the possible involvement of cellular salt, NaCl, in urea-methylamine counteraction on protein stability and function. We found that NaCl mediates methylamine counteracting system from no or partial counteraction to complete counteraction of urea's effect on protein stability and function. These conclusions were drawn from the systematic thermodynamic stability and functional activity measurements of lysozyme and RNase-A. Our results revealed that salts might be involved in protein interaction with charged osmolytes and hence in the urea-methylamine counteraction.
- Subjects :
- lcsh:Medicine
Methylamines
chemistry.chemical_compound
Protein structure
Urea
Denaturation (biochemistry)
lcsh:Science
Multidisciplinary
Protein Stability
Methylamine
lcsh:R
Proteins
Ribonuclease, Pancreatic
Hydrogen-Ion Concentration
Enzyme Activation
chemistry
Biochemistry
Osmolyte
Thermodynamics
lcsh:Q
Muramidase
Salts
Chemical stability
Lysozyme
Research Article
Subjects
Details
- ISSN :
- 19326203
- Volume :
- 10
- Database :
- OpenAIRE
- Journal :
- PLOS ONE
- Accession number :
- edsair.doi.dedup.....a5aa2e9aee70bc09e5fa79eb318e8356