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Single Molecule Manipulation and Sensing with the Atomic Force Microscope

Published online by Cambridge University Press:  02 July 2020

S.M. Lindsay
Affiliation:
Department of Physics and Astronomy, Arizona State University, Tempe, AZ85287
S. H. Leuba
Affiliation:
Physical Molecular Biology, LRBGE, National Cancer Institute, NIH, Bethesda, MD20892 , USA
J. Zlatanova
Affiliation:
Argonne National Laboratory, Argonne, IL60439, USA
M. A. Karymov
Affiliation:
Physical Molecular Biology, LRBGE, National Cancer Institute, NIH, Bethesda, MD20892 , USA
R. Bash
Affiliation:
Department of Chemistry and Biochemistry, Tempe, AZ85287
Y-Z. Liu
Affiliation:
Department of Physics and Astronomy, Arizona State University, Tempe, AZ85287
D. Lohr
Affiliation:
Department of Chemistry and Biochemistry, Tempe, AZ85287
R. E. Harrington
Affiliation:
Department of Microbiology, Arizona State University, Tempe, AZ85287
X.D. Cui
Affiliation:
Department of Physics and Astronomy, Arizona State University, Tempe, AZ85287
X. Zarate
Affiliation:
Department of Chemistry and Biochemistry, Tempe, AZ85287
E. Perez
Affiliation:
Department of Physics and Astronomy, Arizona State University, Tempe, AZ85287
A. Moore
Affiliation:
Department of Chemistry and Biochemistry, Tempe, AZ85287
T.A. Moore
Affiliation:
Department of Chemistry and Biochemistry, Tempe, AZ85287
D. Gust
Affiliation:
Department of Microbiology, Arizona State University, Tempe, AZ85287
O.F. Sankey
Affiliation:
Department of Physics and Astronomy, Arizona State University, Tempe, AZ85287
J. Thomfor
Affiliation:
Department of Physics and Astronomy, Arizona State University, Tempe, AZ85287
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Extract

The atomic force microscope (AFM) can be used both to manipulate molecules and to make measurements on individual molecules. Here, we describe manipulation of chromatin constructs as an example of the first type of measurement, and electronic measurements on single molecules as an example of the second type.

An AFM was used to both image and stretch single synthetic chromatin fibers consisting of twelve core nucleosomes with no linker histones. Peaks in the force-curves are attributed to sequential detachment of nucleosomes from the glass support (Figure 1). The short distances between peaks and reversibility of the pulling process show that the nucleosomes remain intact even at tensions on the order of 350 picoNewtons (pN). This is more than an order of magnitude larger than the force required to de-spool histone octamers from the nucleosomal DNA in laser optical tweezer measurements made with longer molecules, suggesting that loading rates and sample size are important factors in determining the force required to break inter-molecular bonds.

Type
Biomaterials
Copyright
Copyright © Microscopy Society of America

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