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MALDI analysis of oligonucleotides directly from montmorillonite.

Identifieur interne : 002248 ( PubMed/Curation ); précédent : 002247; suivant : 002249

MALDI analysis of oligonucleotides directly from montmorillonite.

Auteurs : Dmitri V. Zagorevskii [États-Unis] ; Michael F. Aldersley ; James P. Ferris

Source :

RBID : pubmed:16809045

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English descriptors

Abstract

Oligonucleotides synthesized on a montmorillonite catalyst were analyzed directly. By mixing the catalyst with a matrix (2,4,6-trihydroxyacetophenone or 6-aza-2-thiothymine) and dibasic ammonium citrate, higher molecular weight products were detected compared with "classical" methods such as gel electrophoresis and HPLC with UV as a detector. The oligomers (30-mers and higher) were detected by mass spectrometry even though their concentration was less than 10(-4)% of the total content of the RNA. This method is different from the (MALDI) analysis of the eluates from montmorillonite, which otherwise requires desalting. Placing reaction mixtures with a high concentration of buffers on homoionic, preferably Li-containing, montmorillonite does not require desalting.

DOI: 10.1016/j.jasms.2006.05.012
PubMed: 16809045

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Le document en format XML

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<div type="abstract" xml:lang="en">Oligonucleotides synthesized on a montmorillonite catalyst were analyzed directly. By mixing the catalyst with a matrix (2,4,6-trihydroxyacetophenone or 6-aza-2-thiothymine) and dibasic ammonium citrate, higher molecular weight products were detected compared with "classical" methods such as gel electrophoresis and HPLC with UV as a detector. The oligomers (30-mers and higher) were detected by mass spectrometry even though their concentration was less than 10(-4)% of the total content of the RNA. This method is different from the (MALDI) analysis of the eluates from montmorillonite, which otherwise requires desalting. Placing reaction mixtures with a high concentration of buffers on homoionic, preferably Li-containing, montmorillonite does not require desalting.</div>
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