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Determination of Sedimentation Coefficients for Small Peptides

Overview
Journal Biophys J
Publisher Cell Press
Specialty Biophysics
Date 1998 Feb 4
PMID 9449347
Citations 30
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Abstract

Direct fitting of sedimentation velocity data with numerical solutions of the Lamm equations has been exploited to obtain sedimentation coefficients for single solutes under conditions where solvent and solution plateaus are either not available or are transient. The calculated evolution was initialized with the first experimental scan and nonlinear regression was employed to obtain best-fit values for the sedimentation and diffusion coefficients. General properties of the Lamm equations as data analysis tools were examined. This method was applied to study a set of small peptides containing amphipathic heptad repeats with the general structure Ac-YS-(AKEAAKE)nGAR-NH2, n = 2, 3, or 4. Sedimentation velocity analysis indicated single sedimenting species with sedimentation coefficients (s(20,w) values) of 0.37, 0.45, and 0.52 S, respectively, in good agreement with sedimentation coefficients predicted by hydrodynamic theory. The described approach can be applied to synthetic boundary and conventional loading experiments, and can be extended to analyze sedimentation data for both large and small macromolecules in order to define shape, heterogeneity, and state of association.

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References
1.
MULHERN T, Howlett G, Reid G, Simpson R, McColl D, Anders R . Solution structure of a polypeptide containing four heptad repeat units from a merozoite surface antigen of Plasmodium falciparum. Biochemistry. 1995; 34(11):3479-91. DOI: 10.1021/bi00011a001. View

2.
Jackson R, Baker H, Gilliam E, Gotto Jr A . Primary structure of very low density apolipoprotein C-II of human plasma. Proc Natl Acad Sci U S A. 1977; 74(5):1942-5. PMC: 431048. DOI: 10.1073/pnas.74.5.1942. View

3.
Claverie J, Dreux H, Cohen R . Sedimentation of generalized systems of interacting particles. I. Solution of systems of complete Lamm equations. Biopolymers. 1975; 14(8):1685-1700. DOI: 10.1002/bip.1975.360140811. View

4.
Garcia de la Torre J, Carrasco B, Harding S . SOLPRO: theory and computer program for the prediction of SOLution PROperties of rigid macromolecules and bioparticles. Eur Biophys J. 1997; 25(5-6):361-72. DOI: 10.1007/s002490050049. View

5.
Howlett G, SCHACHMAN H . Allosteric regulation of aspartate transcarbamoylase. Changes in the sedimentation coefficient promoted by the bisubstrate analogue N-(phosphonacetyl)-L-aspartate. Biochemistry. 1977; 16(23):5077-83. DOI: 10.1021/bi00642a021. View