2004
Refinement of Trypanosoma U6 RNA Stem-Loop Structure Using 1- and 2-Bond Residual Dipolar Couplings
NOVÁK, Petr; Lukáš ŽÍDEK; Petr PADRTA and Vladimír SKLENÁŘBasic information
Original name
Refinement of Trypanosoma U6 RNA Stem-Loop Structure Using 1- and 2-Bond Residual Dipolar Couplings
Name in Czech
Rafinace struktury Trypanosoma U6 RNA s využitím jedno- a dvouvazebných zbytkových dipolárních interakcí
Authors
NOVÁK, Petr (203 Czech Republic); Lukáš ŽÍDEK (203 Czech Republic); Petr PADRTA (203 Czech Republic) and Vladimír SKLENÁŘ (203 Czech Republic, guarantor)
Edition
Brno, 19th NMR Valtice, p. 30-30, 1 pp. 2004
Publisher
Masarykova universita v Brně
Other information
Language
English
Type of outcome
Proceedings paper
Field of Study
10600 1.6 Biological sciences
Country of publisher
Czech Republic
Confidentiality degree
is not subject to a state or trade secret
RIV identification code
RIV/00216224:14310/04:00011133
Organization unit
Faculty of Science
ISBN
80-210-3352-5
Keywords in English
NMR; Residual dipolar couplings; RNA; structure;
Tags
Changed: 31/5/2005 13:42, Mgr. Petr Novák, Ph.D.
In the original language
The spliceosome is a complex of proteins and small nuclear RNAs (snRNAs) responsible for the removal of introns from pre-mRNA in eukaryotes. U6 snRNA has been demonstrated to be a vital element in splicing and its sequence is the most conserved of all snRNAs[1]. U6 snRNA from trypanosoma was our study. Determination of the solution structure of nucleic acid fragments is significantly improved if residual dipolar are measured. This data provides us additional long-range and local geometry restraints using a small degree of molecular alignment with the static magnetic field. We wanted to test polyethylenglycol (PEG) as a alignment medium for measuring the residual dipolar couplings (RDCs). PEG is a stable and unexpensive organic polymer that does not require a complex biochemical preparation like the most often used bacteriophage Pf1. In our study, applicability of PEG to several spin-state-selective E.COSY experiments was investigated. Measured RDCs were tested for internal consistency as refered in [2] in order to check the reliability of the values obtained in the PEG-aligned samples.
In Czech
Rafinace struktury Trypanosoma U6 RNA s využitím jedno- a dvouvazebných zbytkových dipolárních interakcí.
Links
LN00A016, research and development project |
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