th - 1988 - 51st ENC Conference
th - 1988 - 51st ENC Conference
th - 1988 - 51st ENC Conference
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-- 150 I ISOTOPE DETECTED NOE EXPERIMENTS ON 13C LABELED tRNAPhe: William<br />
H. Gmeiner*and C. Dale Poulter, Department of Chemistry, University<br />
of Utah, Salt Lake City, UT 84112<br />
Isotope directed and isotope detected nuclear Overhauser effect experiments are<br />
performed on tRNA^ ne from E. coli in which all <strong>th</strong>e adenine residues were labeled at<br />
position 8 wi<strong>th</strong> ±jC. The experiments are used to establish <strong>th</strong>e presence of <strong>th</strong>e<br />
unusual Hoogsteen type base-pair in <strong>th</strong>e solution structure of <strong>th</strong>e molecule. A<br />
relaxation p~file of <strong>th</strong>e lab~edlsite is presented in which <strong>th</strong>e effect of two<br />
quadrupolar --N spins on <strong>th</strong>e -C- H spin system is analyzed. The rel~ation effect<br />
on <strong>th</strong>e imino proton of uridine in adenosine-uridine base-pairs by <strong>th</strong>e--C label is<br />
used to measure <strong>th</strong>e relative populations of Watson-Crick and Hoogsteen base-pairs in<br />
a chloroform soluble model system.<br />
- - isi<br />
I<br />
Inversion Recovery Cross Polarization (IRCP) techniques are used to probe <strong>th</strong>e<br />
structures of morphologlcally different polye<strong>th</strong>ylenes. Crystalline and amorphous<br />
components were resolved by <strong>th</strong>eir different cross polarization (CP) rates which were<br />
discriminated by an IRCP pulse sequence. At least two major magnetically distinct<br />
environments were detected in each sample. The arystalllne-amorphous interfaclal<br />
domains were also detected in some samples. The cross polarization time, TCH, of<br />
each phase was compared among <strong>th</strong>ese morphologically different samples and can be<br />
interpreted in terms of structural details.<br />
The effect on TCH by varying magic angle spinning speed and spln-lock power<br />
were also studied. The chemical shift anlsotropy (CSA) of each component and <strong>th</strong>e<br />
degree of crystalllnlty of <strong>th</strong>ese semicrystalllne polymers were also discussed in <strong>th</strong>e<br />
study.<br />
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