Macromolecular dynamics studied by magnetic resonance and neutron scattering
| dc.contributor.advisor | Rorschach, Harold E., Jr. | |
| dc.creator | Lin, Chen | |
| dc.date.accessioned | 2009-06-04T00:31:25Z | |
| dc.date.available | 2009-06-04T00:31:25Z | |
| dc.date.issued | 1992 | |
| dc.description.abstract | Macromolecular dynamics is important for both understanding biological processes and practical applications such as MR imaging data interpretation. We have used the QNS method to study the dynamics of trypsin chain segments. Trypsin powder and trypsin in D$\sb2$O were studied for temperatures from 100K to 300K. Energy spectra of the scattered neutrons were measured for various neutron momentum transfer. Diffusive type motion of chain segments are observed for trypsin solutions at temperatures above the freezing point, while powder and frozen samples display minimum chain motion. The motion of trypsin chain segments can be fitted by a general "jump-diffusion" model which describes the conformational changes of a macromolecule as transitions between its substates. The diffusion coefficient of the trypsin chain segment is 2.4 $\times$ 10$\sp{-6}$ cm$\sp2$/sec and the average residence time of trypsin in its substates is 1.3 $\times$ 10$\sp{-11}$ second when trypsin is in D$\sb2$O at 300K. We measured the average mean square thermal vibration amplitude of trypsin (0.65 A$\sp2$) which is slightly larger than the results from computer simulations and X-ray diffraction studies. We also have tested macromolecular dynamics theory on poly-acrylic acid. We measured the frequency dependence of proton T$\sb1$ relaxation rates of poly-acrylic acid in D$\sb2$O solutions with different pDs and salt concentrations. Frequency dispersion data analyzed using both a flexible chain model and a stiff chain model give a maximum correlation time of 1.5-2.3 $\times$ 10$\sp{-7}$ second depends on the model. No significant change due pD and salt concentration difference was found. | |
| dc.format.extent | 92 p. | en_US |
| dc.format.mimetype | application/pdf | |
| dc.identifier.callno | Thesis Phys. 1992 Lin | |
| dc.identifier.citation | Lin, Chen. "Macromolecular dynamics studied by magnetic resonance and neutron scattering." (1992) Diss., Rice University. <a href="https://hdl.handle.net/1911/16579">https://hdl.handle.net/1911/16579</a>. | |
| dc.identifier.uri | https://hdl.handle.net/1911/16579 | |
| dc.language.iso | eng | |
| dc.rights | Copyright is held by the author, unless otherwise indicated. Permission to reuse, publish, or reproduce the work beyond the bounds of fair use or other exemptions to copyright law must be obtained from the copyright holder. | |
| dc.subject | Biophysics | |
| dc.subject | Molecular physics | |
| dc.title | Macromolecular dynamics studied by magnetic resonance and neutron scattering | |
| dc.type | Thesis | |
| dc.type.material | Text | |
| thesis.degree.department | Physics | |
| thesis.degree.discipline | Natural Sciences | |
| thesis.degree.grantor | Rice University | |
| thesis.degree.level | Doctoral | |
| thesis.degree.name | Doctor of Philosophy |
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