Dissertation/Thesis Abstract

Exploring the potential of protein cages as MRI contrast agents with an emphasis on protein cage characterization by mass spectrometry techniques
by Liepold, Lars Otto, Ph.D., Montana State University, 2009, 197; 3379898
Abstract (Summary)

Described here is the development of a protein cages as efficient and potentially relevant MRI contrast agents. Three approaches are outlined to fuse high affinity Gd3+ chelating moieties to the surfaces of protein cages. In the first approach, a metal binding peptide has been genetically engineered into the subunit of Cowpea chlorotic mottle virus (CCMV) and to the small heat shock protein cage from Methanococcus jannaschii (HSP). The genetic fusion resulted in a 200x binding enhancement of Gd3+ to CCMV in comparison with wild type CCMV and metal binding functionality was added to the HSP protein cage. In a second approach DOTA-Gd was attached to CCMV by reactions with endogenous lysine residues on the surface of the viral capsids and resulted in r1 = 2,806 at 61 MHz for the 28nm diameter particle.

Directed by the results of earlier generations of protein cage based contrast agents a next generation MRI contrast agent was designed. In this work a DTPA-Gd containing polymer was grown in the interior of HSP resulting in T1 particle relaxivities of 4,200mM-1 sec -1 for the 12nm particle. Relaxivity parameters were determined and this analysis suggests that the rotational correlation time of the Gd 3+ chelate has been optimized while the exchange life time of Gd 3+-bound water is slower than optimal. This synthetic approach holds much promise for the development of future generations of contrast agents.

Throughout the evolution of the protein cage based contrast agents there has also been and evolution of our ability to characterize these cages with mass spectrometric techniques. Specifically refined methodologies are presented for QT of characterization of protein cage at the level of amino acids, protein subunits, protein complexes and their cellular expression. Furthermore, correct charge state assignment is crucial to assigning an accurate mass to supramolecular complexes such as protein cages analyzed by electrospray mass spectrometry. Conventional charge state assignment techniques fall short of reliably and unambiguously predicting the correct charge state for many supramolecular complexes. We provide an explanation of the shortcomings of the conventional techniques and have developed a robust charge state assignment method that is applicable to all spectra.

Indexing (document details)
Advisor: Douglas, Trevor, Young, Mark
Commitee: Bothner, Brian, Cloninger, Mary, Teintze, Martin
School: Montana State University
Department: Chemistry and Biochemistry
School Location: United States -- Montana
Source: DAI-B 70/12, Dissertation Abstracts International
Source Type: DISSERTATION
Subjects: Analytical chemistry, Biochemistry, Physical chemistry
Keywords: Contrast agents, Electrospray ionization, Gadolinium, Magnetic resonance imaging, Native spray, Protein cages
Publication Number: 3379898
ISBN: 978-1-109-49729-8
Copyright © 2019 ProQuest LLC. All rights reserved. Terms and Conditions Privacy Policy Cookie Policy
ProQuest