| Literature DB >> 2498751 |
Abstract
We have developed a method for the isolation of a brain subcellular fraction enriched in both highly aggregated polyribosomes and cytoskeletal proteins. This method is based on gentle homogenization of brain tissue and low speed centrifugation. The mechanism of association of polyribosomes to cytoskeletal structures has been studied by in vitro treatment of this fraction with polyribosome-disaggregating agents. RNase and EDTA, while succeeding in completely disrupting them into monosomes or subunits, did not release them from cytoskeleton. Puromycin showed no noticeable effect.Entities:
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Year: 1989 PMID: 2498751 DOI: 10.1007/bf00971317
Source DB: PubMed Journal: Neurochem Res ISSN: 0364-3190 Impact factor: 3.996