Aminopeptidases do not directly degrade tau protein

<p>Abstract</p> <p>Background</p> <p>Tau hyperphosphorylation and aggregation to form intracellular neurofibrillar tangles is prevalent in a number of tauopathies. Thus there is current interest in the mechanisms involved in Tau clearance. It was recently reported that...

Full description

Bibliographic Details
Main Authors: Hersh Louis B, Guan Hanjun, Chow K
Format: Article
Language:English
Published: BMC 2010-11-01
Series:Molecular Neurodegeneration
Online Access:http://www.molecularneurodegeneration.com/content/5/1/48
id doaj-c76a7584391e44e2a6dffa7bf1248bbd
record_format Article
spelling doaj-c76a7584391e44e2a6dffa7bf1248bbd2020-11-24T22:06:28ZengBMCMolecular Neurodegeneration1750-13262010-11-01514810.1186/1750-1326-5-48Aminopeptidases do not directly degrade tau proteinHersh Louis BGuan HanjunChow K<p>Abstract</p> <p>Background</p> <p>Tau hyperphosphorylation and aggregation to form intracellular neurofibrillar tangles is prevalent in a number of tauopathies. Thus there is current interest in the mechanisms involved in Tau clearance. It was recently reported that Tau can be degraded by an aminopeptidase known as the puromycin sensitive aminopeptidase (PSA). Until now PSA has been reported to only cleave peptides, with the largest reported substrates having 30-50 amino acids. We have studied this unique PSA cleavage reaction using a number of different PSA preparations.</p> <p>Results</p> <p>An N-terminally His tagged-PSA was expressed and purified from Sf9 insect cells. Although this PSA preparation cleaved Tau, product analysis with N and C terminal Tau antibodies coupled with mass spectrometry showed an endoproteolytic cleavage atypical for an aminopeptidase. Furthermore, the reaction was not blocked by the general aminopeptidase inhibitor bestatin or the specific PSA inhibitor puromycin. In order to test whether Tau hydrolysis might be caused by a protease contaminant the enzyme was expressed in E. coli as glutathione S-transferase and maltose binding protein fusion proteins or in Sf9 cells as a C-terminally His-tagged protein. After purification to near homogeneity none of these other recombinant forms of PSA cleaved Tau. Further, Tau-cleaving activity and aminopeptidase activities derived from the Sf9 cell expression system were separable by molecular sieve chromatography. When tested in a cellular context we again failed to see a PSA dependent cleavage of Tau. A commercial preparation of a related aminopeptidase, aminopeptidase N, also exhibited Tau cleaving activity, but this activity could also be separated from aminopeptidase activity.</p> <p>Conclusion</p> <p>It is concluded that PSA does not directly cleave Tau.</p> http://www.molecularneurodegeneration.com/content/5/1/48
collection DOAJ
language English
format Article
sources DOAJ
author Hersh Louis B
Guan Hanjun
Chow K
spellingShingle Hersh Louis B
Guan Hanjun
Chow K
Aminopeptidases do not directly degrade tau protein
Molecular Neurodegeneration
author_facet Hersh Louis B
Guan Hanjun
Chow K
author_sort Hersh Louis B
title Aminopeptidases do not directly degrade tau protein
title_short Aminopeptidases do not directly degrade tau protein
title_full Aminopeptidases do not directly degrade tau protein
title_fullStr Aminopeptidases do not directly degrade tau protein
title_full_unstemmed Aminopeptidases do not directly degrade tau protein
title_sort aminopeptidases do not directly degrade tau protein
publisher BMC
series Molecular Neurodegeneration
issn 1750-1326
publishDate 2010-11-01
description <p>Abstract</p> <p>Background</p> <p>Tau hyperphosphorylation and aggregation to form intracellular neurofibrillar tangles is prevalent in a number of tauopathies. Thus there is current interest in the mechanisms involved in Tau clearance. It was recently reported that Tau can be degraded by an aminopeptidase known as the puromycin sensitive aminopeptidase (PSA). Until now PSA has been reported to only cleave peptides, with the largest reported substrates having 30-50 amino acids. We have studied this unique PSA cleavage reaction using a number of different PSA preparations.</p> <p>Results</p> <p>An N-terminally His tagged-PSA was expressed and purified from Sf9 insect cells. Although this PSA preparation cleaved Tau, product analysis with N and C terminal Tau antibodies coupled with mass spectrometry showed an endoproteolytic cleavage atypical for an aminopeptidase. Furthermore, the reaction was not blocked by the general aminopeptidase inhibitor bestatin or the specific PSA inhibitor puromycin. In order to test whether Tau hydrolysis might be caused by a protease contaminant the enzyme was expressed in E. coli as glutathione S-transferase and maltose binding protein fusion proteins or in Sf9 cells as a C-terminally His-tagged protein. After purification to near homogeneity none of these other recombinant forms of PSA cleaved Tau. Further, Tau-cleaving activity and aminopeptidase activities derived from the Sf9 cell expression system were separable by molecular sieve chromatography. When tested in a cellular context we again failed to see a PSA dependent cleavage of Tau. A commercial preparation of a related aminopeptidase, aminopeptidase N, also exhibited Tau cleaving activity, but this activity could also be separated from aminopeptidase activity.</p> <p>Conclusion</p> <p>It is concluded that PSA does not directly cleave Tau.</p>
url http://www.molecularneurodegeneration.com/content/5/1/48
work_keys_str_mv AT hershlouisb aminopeptidasesdonotdirectlydegradetauprotein
AT guanhanjun aminopeptidasesdonotdirectlydegradetauprotein
AT chowk aminopeptidasesdonotdirectlydegradetauprotein
_version_ 1725823549109698560