| pubmed-article:17635931 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:17635931 | lifeskim:mentions | umls-concept:C0596402 | lld:lifeskim |
| pubmed-article:17635931 | lifeskim:mentions | umls-concept:C0035542 | lld:lifeskim |
| pubmed-article:17635931 | lifeskim:mentions | umls-concept:C1521761 | lld:lifeskim |
| pubmed-article:17635931 | pubmed:issue | 38 | lld:pubmed |
| pubmed-article:17635931 | pubmed:dateCreated | 2007-9-14 | lld:pubmed |
| pubmed-article:17635931 | pubmed:abstractText | The cytotoxic action of ribonucleases (RNases) requires the interaction of the enzyme with the cellular membrane, its internalization, translocation to the cytosol, and the degradation of ribonucleic acid. The interplay of these processes as well as the role of the thermodynamic and proteolytic stability, the catalytic activity, and the evasion from the intracellular ribonuclease inhibitor (RI) has not yet been fully elucidated. As cytosolic internalization is indispensable for the cytotoxicity of extracellular ribonucleases, we investigated the extent of cytosolic internalization of a cytotoxic, RI-evasive RNase A variant (G88R-RNase A) and of various similarly cytotoxic but RI-sensitive RNase A tandem enzyme variants in comparison to the internalization of the non-cytotoxic and RI-sensitive RNase A. After incubation of K-562 cells with the RNase A variants for 36 h, the internalized amount of RNases was analyzed by rapid cell disruption followed by subcellular fractionation and semiquantitative immunoblotting. The data indicate that an enhanced cellular uptake and an increased entry of the RNases into the cytosol can outweigh the abolishment of catalytic activity by RI. As all RNase A variants proved to be resistant to the proteases present in the different subcellular fractions for more than 100 h, our results suggest that the cytotoxic potency of RNases is determined by an efficient internalization into the cytosol. | lld:pubmed |
| pubmed-article:17635931 | pubmed:language | eng | lld:pubmed |
| pubmed-article:17635931 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:17635931 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:17635931 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:17635931 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:17635931 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:17635931 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:17635931 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:17635931 | pubmed:month | Sep | lld:pubmed |
| pubmed-article:17635931 | pubmed:issn | 0021-9258 | lld:pubmed |
| pubmed-article:17635931 | pubmed:author | pubmed-author:Ulbrich-Hofma... | lld:pubmed |
| pubmed-article:17635931 | pubmed:author | pubmed-author:ArnoldUlrichU | lld:pubmed |
| pubmed-article:17635931 | pubmed:author | pubmed-author:LeichFranzisk... | lld:pubmed |
| pubmed-article:17635931 | pubmed:author | pubmed-author:StöhrNadineN | lld:pubmed |
| pubmed-article:17635931 | pubmed:author | pubmed-author:RietzAnneA | lld:pubmed |
| pubmed-article:17635931 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:17635931 | pubmed:day | 21 | lld:pubmed |
| pubmed-article:17635931 | pubmed:volume | 282 | lld:pubmed |
| pubmed-article:17635931 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:17635931 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:17635931 | pubmed:pagination | 27640-6 | lld:pubmed |
| pubmed-article:17635931 | pubmed:meshHeading | pubmed-meshheading:17635931... | lld:pubmed |
| pubmed-article:17635931 | pubmed:meshHeading | pubmed-meshheading:17635931... | lld:pubmed |
| pubmed-article:17635931 | pubmed:meshHeading | pubmed-meshheading:17635931... | lld:pubmed |
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| pubmed-article:17635931 | pubmed:meshHeading | pubmed-meshheading:17635931... | lld:pubmed |
| pubmed-article:17635931 | pubmed:meshHeading | pubmed-meshheading:17635931... | lld:pubmed |
| pubmed-article:17635931 | pubmed:meshHeading | pubmed-meshheading:17635931... | lld:pubmed |
| pubmed-article:17635931 | pubmed:meshHeading | pubmed-meshheading:17635931... | lld:pubmed |
| pubmed-article:17635931 | pubmed:meshHeading | pubmed-meshheading:17635931... | lld:pubmed |
| pubmed-article:17635931 | pubmed:meshHeading | pubmed-meshheading:17635931... | lld:pubmed |
| pubmed-article:17635931 | pubmed:meshHeading | pubmed-meshheading:17635931... | lld:pubmed |
| pubmed-article:17635931 | pubmed:meshHeading | pubmed-meshheading:17635931... | lld:pubmed |
| pubmed-article:17635931 | pubmed:meshHeading | pubmed-meshheading:17635931... | lld:pubmed |
| pubmed-article:17635931 | pubmed:meshHeading | pubmed-meshheading:17635931... | lld:pubmed |
| pubmed-article:17635931 | pubmed:year | 2007 | lld:pubmed |
| pubmed-article:17635931 | pubmed:articleTitle | Endocytotic internalization as a crucial factor for the cytotoxicity of ribonucleases. | lld:pubmed |
| pubmed-article:17635931 | pubmed:affiliation | Institute of Biochemistry and Biotechnology, Martin Luther University Halle-Wittenberg, Halle, Germany. | lld:pubmed |
| pubmed-article:17635931 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:17635931 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
| http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:17635931 | lld:pubmed |
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| http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:17635931 | lld:pubmed |
