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.
Full Text
The Full Text of this article is available as a PDF (104.9 KB).
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Biemann K. Mass spectrometry of peptides and proteins. Annu Rev Biochem. 1992;61:977–1010. doi: 10.1146/annurev.bi.61.070192.004553. [DOI] [PubMed] [Google Scholar]
- Fenn J. B., Mann M., Meng C. K., Wong S. F., Whitehouse C. M. Electrospray ionization for mass spectrometry of large biomolecules. Science. 1989 Oct 6;246(4926):64–71. doi: 10.1126/science.2675315. [DOI] [PubMed] [Google Scholar]
- Greig M., Griffey R. H. Utility of organic bases for improved electrospray mass spectrometry of oligonucleotides. Rapid Commun Mass Spectrom. 1995;9(1):97–102. doi: 10.1002/rcm.1290090121. [DOI] [PubMed] [Google Scholar]
- Hayashi N., Suzuki M., Titani K., Taniguchi H. Structural studies of tRNAs by capillary high performance liquid chromatography/electrospray mass spectrometry. Nucleic Acids Symp Ser. 1995;(34):153–154. [PubMed] [Google Scholar]
- Hillenkamp F., Karas M. Mass spectrometry of peptides and proteins by matrix-assisted ultraviolet laser desorption/ionization. Methods Enzymol. 1990;193:280–295. doi: 10.1016/0076-6879(90)93420-p. [DOI] [PubMed] [Google Scholar]
- Holmes W. M., Hurd R. E., Reid B. R., Rimerman R. A., Hatfield G. W. Separation of transfer ribonucleic acid by sepharose chromatography using reverse salt gradients. Proc Natl Acad Sci U S A. 1975 Mar;72(3):1068–1071. doi: 10.1073/pnas.72.3.1068. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kowalak J. A., Bruenger E., McCloskey J. A. Posttranscriptional modification of the central loop of domain V in Escherichia coli 23 S ribosomal RNA. J Biol Chem. 1995 Jul 28;270(30):17758–17764. doi: 10.1074/jbc.270.30.17758. [DOI] [PubMed] [Google Scholar]
- Kowalak J. A., Pomerantz S. C., Crain P. F., McCloskey J. A. A novel method for the determination of post-transcriptional modification in RNA by mass spectrometry. Nucleic Acids Res. 1993 Sep 25;21(19):4577–4585. doi: 10.1093/nar/21.19.4577. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Limbach P. A., Crain P. F., McCloskey J. A. Characterization of oligonucleotides and nucleic acids by mass spectrometry. Curr Opin Biotechnol. 1995 Feb;6(1):96–102. doi: 10.1016/0958-1669(95)80015-8. [DOI] [PubMed] [Google Scholar]
- Little D. P., Thannhauser T. W., McLafferty F. W. Verification of 50- to 100-mer DNA and RNA sequences with high-resolution mass spectrometry. Proc Natl Acad Sci U S A. 1995 Mar 14;92(6):2318–2322. doi: 10.1073/pnas.92.6.2318. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Manenti S., Sorokine O., Van Dorsselaer A., Taniguchi H. 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. J Biol Chem. 1992 Nov 5;267(31):22310–22315. [PubMed] [Google Scholar]
- Manenti S., Sorokine O., Van Dorsselaer A., Taniguchi H. Demyristoylation of the major substrate of protein kinase C (MARCKS) by the cytoplasmic fraction of brain synaptosomes. J Biol Chem. 1994 Mar 18;269(11):8309–8313. [PubMed] [Google Scholar]
- Manenti S., Sorokine O., Van Dorsselaer A., Taniguchi H. Isolation of the non-myristoylated form of a major substrate of protein kinase C (MARCKS) from bovine brain. J Biol Chem. 1993 Apr 5;268(10):6878–6881. [PubMed] [Google Scholar]
- Matsubara M., Kusubata M., Ishiguro K., Uchida T., Titani K., Taniguchi H. Site-specific phosphorylation of synapsin I by mitogen-activated protein kinase and Cdk5 and its effects on physiological functions. J Biol Chem. 1996 Aug 30;271(35):21108–21113. doi: 10.1074/jbc.271.35.21108. [DOI] [PubMed] [Google Scholar]
- Potier N., Van Dorsselaer A., Cordier Y., Roch O., Bischoff R. Negative electrospray ionization mass spectrometry of synthetic and chemically modified oligonucleotides. Nucleic Acids Res. 1994 Sep 25;22(19):3895–3903. doi: 10.1093/nar/22.19.3895. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Saks M. E., Sampson J. R., Abelson J. N. The transfer RNA identity problem: a search for rules. Science. 1994 Jan 14;263(5144):191–197. doi: 10.1126/science.7506844. [DOI] [PubMed] [Google Scholar]
- Sampson J. R., Uhlenbeck O. C. Biochemical and physical characterization of an unmodified yeast phenylalanine transfer RNA transcribed in vitro. Proc Natl Acad Sci U S A. 1988 Feb;85(4):1033–1037. doi: 10.1073/pnas.85.4.1033. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Seno T., Kobayashi M., Nishimura S. Purification of Excherichia coli methionine tRNAF and methionine tRNAM and studies on their biophysical and biochemical properties. Biochim Biophys Acta. 1968 Nov 20;169(1):80–94. doi: 10.1016/0005-2787(68)90010-5. [DOI] [PubMed] [Google Scholar]
- Shimizu M., Asahara H., Tamura K., Hasegawa T., Himeno H. The role of anticodon bases and the discriminator nucleotide in the recognition of some E. coli tRNAs by their aminoacyl-tRNA synthetases. J Mol Evol. 1992 Nov;35(5):436–443. doi: 10.1007/BF00171822. [DOI] [PubMed] [Google Scholar]
- Sprinzl M., Dank N., Nock S., Schön A. Compilation of tRNA sequences and sequences of tRNA genes. Nucleic Acids Res. 1991 Apr 25;19 (Suppl):2127–2171. doi: 10.1093/nar/19.suppl.2127. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Sprinzl M., Hartmann T., Meissner F., Moll J., Vorderwülbecke T. Compilation of tRNA sequences and sequences of tRNA genes. Nucleic Acids Res. 1987;15 (Suppl):r53–188. doi: 10.1093/nar/15.suppl.r53. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Sprinzl M., Hartmann T., Weber J., Blank J., Zeidler R. Compilation of tRNA sequences and sequences of tRNA genes. Nucleic Acids Res. 1989;17 (Suppl):r1–172. doi: 10.1093/nar/17.suppl.r1. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Sprinzl M., Vorderwülbecke T., Hartmann T. Compilation of sequences of tRNA genes. Nucleic Acids Res. 1985;13 (Suppl):r51–104. doi: 10.1093/nar/13.suppl.r51. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Taniguchi H., Manenti S., Suzuki M., Titani K. Myristoylated alanine-rich C kinase substrate (MARCKS), a major protein kinase C substrate, is an in vivo substrate of proline-directed protein kinase(s). A mass spectroscopic analysis of the post-translational modifications. J Biol Chem. 1994 Jul 15;269(28):18299–18302. [PubMed] [Google Scholar]
- Taniguchi H., Suzuki M., Manenti S., Titani K. A mass spectrometric study on the in vivo posttranslational modification of GAP-43. J Biol Chem. 1994 Sep 9;269(36):22481–22484. [PubMed] [Google Scholar]
- Watanabe K., Hayashi N., Oyama A., Nishikawa K., Ueda T., Miura K. Unusual anticodon loop structure found in E.coli lysine tRNA. Nucleic Acids Res. 1994 Jan 11;22(1):79–87. doi: 10.1093/nar/22.1.79. [DOI] [PMC free article] [PubMed] [Google Scholar]
