help button home button Biophys. J.
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS

Originally published as Biophys J. BioFAST on September 17, 2004.
doi:10.1529/biophysj.104.048983
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
biophysj.104.048983v1
87/6/4135    most recent
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
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 HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Nikova, D. N.
Right arrow Articles by Greve, J.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Nikova, D. N.
Right arrow Articles by Greve, J.
Biophysical Journal 87:4135-4145 (2004)
© 2004 The Biophysical Society

Unexpected Binding Motifs for Subnucleosomal Particles Revealed by Atomic Force Microscopy

Dessy N. Nikova * {ddagger}, Lisa H. Pope * ¶, Martin L. Bennink * {dagger}, Kirsten A. van Leijenhorst-Groener *, Kees van der Werf * and Jan Greve *

* Biophysical Techniques, Department of Science and Technology, and {dagger} MESA+ Research Institute, University of Twente, Enschede, The Netherlands; {ddagger} University of Muenster, Institute of Physiology, Muenster, Germany; and University of Illinois at Chicago, Department of Physics, Chicago, Illinois USA

Correspondence: Address reprint requests to D. N. Nikova, University of Muenster, Institute of Physiology, 27b Robert Koch St., 48149 Muenster, Germany. Tel.: 49-251-8355336; Fax: 49-251-8355331; E-mail: nikovad{at}uni-muenster.de.

The structure of individual nucleosomes organized within reconstituted 208-12 arrays at different levels of compaction was examined by tapping mode atomic force microscopy in air and liquid. Reconstitution at lower histone octamer to DNA weight ratios showed an extended beads-on-a-string morphology with less than the expected maximum of 12 nucleosome core particles per array, each particle located in the most favored positioning site. A correlation of the contour lengths of these arrays with the number of observed particles revealed two distinct populations of particles, one with ~50 nm of bound DNA and a second population with ~25 nm. The measured nucleosome center-to-center distances indicate that this ~25 nm is not necessarily symmetrically bound about the dyad axis, but can also correspond to DNA bound from either the entry or exit point of the particle to a location at or close to the dyad axis. An assessment of particle heights suggests that particles wrapping ~25 nm of DNA are most likely to be subnucleosomal particles, which lack either one or both H2A-H2B dimers. At a higher reconstitution ratio, folded compact arrays fully populated with 12 nucleosome core particles, were observed. Liquid measurements demonstrated dynamic movements of DNA loops protruding from these folded arrays.




This article has been cited by other articles:


Home page
Nucleic Acids ResHome page
M. Engelhardt
Choreography for nucleosomes: the conformational freedom of the nucleosomal filament and its limitations
Nucleic Acids Res., August 13, 2007; 35(16): e106 - e106.
[Abstract] [Full Text] [PDF]


Home page
Biophys. JHome page
F. Montel, E. Fontaine, P. St-Jean, M. Castelnovo, and C. Faivre-Moskalenko
Atomic Force Microscopy Imaging of SWI/SNF Action: Mapping the Nucleosome Remodeling and Sliding
Biophys. J., July 15, 2007; 93(2): 566 - 578.
[Abstract] [Full Text] [PDF]


Home page
Biophys. JHome page
S. Sheng, D. M. Czajkowsky, and Z. Shao
Localization of Linker Histone in Chromatosomes by Cryo-Atomic Force Microscopy
Biophys. J., August 15, 2006; 91(4): L35 - L37.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 2004 by the Biophysical Society.