Interaction of human serum albumin and its clinically relevant modification with oligoribonucleotides

RNA hydrolysis in the presence of HSA proceeds via 2′,3′-cyclophosphate intermediates. Nonenzymatic glycation of HSA decreases protein-mediated oligoribonucleotide cleavage with no influence on the cleavage specificity. Human serum albumin (HSA) was shown to mediate oligoribonucleotide cleavage. Non...

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Veröffentlicht in:Bioorganic & medicinal chemistry 2008-08, Vol.18 (16), p.4511-4514
Hauptverfasser: Gerasimova, Yuliya V., Erchenko, Irina A., Shakirov, Makhmut M., Godovikova, Tatyana S.
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container_end_page 4514
container_issue 16
container_start_page 4511
container_title Bioorganic & medicinal chemistry
container_volume 18
creator Gerasimova, Yuliya V.
Erchenko, Irina A.
Shakirov, Makhmut M.
Godovikova, Tatyana S.
description RNA hydrolysis in the presence of HSA proceeds via 2′,3′-cyclophosphate intermediates. Nonenzymatic glycation of HSA decreases protein-mediated oligoribonucleotide cleavage with no influence on the cleavage specificity. Human serum albumin (HSA) was shown to mediate oligoribonucleotide cleavage. Nonenzymatic glycation of HSA decreased the ribonuclease-like activity of the protein. According to 31P NMR data, both native and glycated albumins induced hydrolysis of RNA molecule through 2′,3′-cyclophosphate intermediates. A feasible mechanism of RNA hydrolysis by native albumin and its clinically relevant modification was discussed.
doi_str_mv 10.1016/j.bmcl.2008.07.060
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source MEDLINE; Elsevier ScienceDirect Journals Complete
subjects Biochemistry - methods
Chromatography, Ion Exchange - methods
Glycation
Human serum albumin
Humans
Hydrolysis
Ligands
Magnetic Resonance Spectroscopy
Models, Chemical
Nucleic Acids - chemistry
Oligoribonucleotides
Oligoribonucleotides - chemistry
Phosphates - chemistry
Protein Binding
RNA - chemistry
RNA-hydrolyzing activity
Serum Albumin - chemistry
Serum Albumin - metabolism
title Interaction of human serum albumin and its clinically relevant modification with oligoribonucleotides
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