Literature DB >> 9490795

A liquid chromatography/electrospray mass spectrometric study on the post-transcriptional modification of tRNA.

H Taniguchi1, N Hayashi.   

Abstract

Liquid chromatography/electrospray mass spectrometry is one of the rapidly developing techniques with which mass of large hydrophilic polymers such as proteins and nucleic acids can be determined precisely. The technique was applied to studies on the modifications of tRNAs. Various tRNA species purified from Escherichia coli were directly injected into a capillary reversed-phase column and the desalted and concentrated tRNAs were analyzed on-line with an electrospray mass spectrometer. In some cases, small but significant differences were noted between the theoretical and observed molecular masses, suggesting that there exist still unknown modifications. Under high resolution measurements, multiple peaks corresponding to species modified to a varying extent were resolved. To study the structures in detail, the isolated tRNA species were digested with ribonuclease T1, and the resulting mixture of fragments were analyzed by the same liquid chromatography/mass spectrometry. In this way, most of the fragments were easily identified solely from their masses, and the positions where the expected and real structures differ were revealed. The results obtained showed the presence of micro-heterogeneity among tRNAs and demonstrated at the same time the power of the hyphenated technique for the structural analysis on nucleic acids.

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Year:  1998        PMID: 9490795      PMCID: PMC147412          DOI: 10.1093/nar/26.6.1481

Source DB:  PubMed          Journal:  Nucleic Acids Res        ISSN: 0305-1048            Impact factor:   16.971


  26 in total

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Review 3.  The transfer RNA identity problem: a search for rules.

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Journal:  Nucleic Acids Res       Date:  1994-01-11       Impact factor: 16.971

9.  Affinity purification and characterization of myristoylated alanine-rich protein kinase C substrate (MARCKS) from bovine brain. Comparison of the cytoplasmic and the membrane-bound forms.

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Authors:  S Manenti; O Sorokine; A Van Dorsselaer; H Taniguchi
Journal:  J Biol Chem       Date:  1994-03-18       Impact factor: 5.157

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2.  The catalytic domain of topological knot tRNA methyltransferase (TrmH) discriminates between substrate tRNA and nonsubstrate tRNA via an induced-fit process.

Authors:  Anna Ochi; Koki Makabe; Ryota Yamagami; Akira Hirata; Reiko Sakaguchi; Ya-Ming Hou; Kazunori Watanabe; Osamu Nureki; Kunihiro Kuwajima; Hiroyuki Hori
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  2 in total

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