Protein Science
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Protein Science (2005), 14:329-340. Published by Cold Spring Harbor Laboratory Press. Copyright © 2005 The Protein Society
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Fast, J.
Right arrow Articles by Linse, S.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Fast, J.
Right arrow Articles by Linse, S.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us   Add to Digg   Add to Reddit   Add to Technorati  
What's this?

Stability of HAMLET—A kinetically trapped {alpha}-lactalbumin oleic acid complex

Jonas Fast1,3, Ann-Kristin Mossberg2, Catharina Svanborg2 and Sara Linse1

1 Department of Biophysical Chemistry and 2 Institute of Laboratory Medicine, Department of Microbiology, Immunology and Glycobiology, Lund University, SE-221 00 Lund, Sweden

(RECEIVED July 9, 2004; FINAL REVISION November 2, 2004; ACCEPTED November 2, 2004)

The stability toward thermal and urea denaturation was measured for HAMLET (human {alpha}-lactalbumin made lethal to tumor cells) and {alpha}-lactalbumin, using circular dichroism and fluorescence spectroscopy as well as differential scanning calorimetry. Under all conditions examined, HAMLET appears to have the same or lower stability than {alpha}-lactalbumin. The largest difference is seen for thermal denaturation of the calcium free (apo) forms, where the temperature at the transition midpoint is 15°C lower for apo HAMLET than for apo {alpha}-lactalbumin. The difference becomes progressively smaller as the calcium concentration increases. Denaturation of HAMLET was found to be irreversible. Samples of HAMLET that have been renatured after denaturation have lost the specific biological activity toward tumor cells. Three lines of evidence indicate that HAMLET is a kinetic trap: (1) It has lower stability than {alpha}-lactalbumin, although it is a complex of {alpha}-lactalbumin and oleic acid; (2) its denaturation is irreversible and HAMLET is lost after denaturation; (3) formation of HAMLET requires a specific conversion protocol.

Keywords: protein stability; protein folding; kinetic trap; {alpha}-lactalbumin

Abbreviations: CD, circular dichroism • DSC, differential scanning calorimetry • EDTA, ethylenediamintetraacetic acid. 1 calorie = 4.185 Joule

Article and publication are at http://www.proteinscience.org/cgi/doi/10.1110/ps.04982905.


Reprint requests to: Jonas Fast, Department of Chemistry and Biochemistry, University of Colorado, Cristol Building, Room 226, Boulder, CO 80309-0215, USA; e-mail: jfast{at}colorado.edu; or Sara Linse, Department of Biophysical Chemistry, Lund University, SE-221 00 Lund, Sweden, e-mail: sara.linse{at}bpc.lu.se; fax: +46-46-2224543.


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Reddit Reddit   Add to Technorati Technorati    What's this?





HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 2005 by The Protein Society.