ATOMIC FORCE MICROSCOPY IMAGING OF DOUBLE-STRANDED DNA AND RNA

被引:141
|
作者
LYUBCHENKO, YL
GALL, AA
SHLYAKHTENKO, LS
HARRINGTON, RE
JACOBS, BL
ODEN, PI
LINDSAY, SM
机构
[1] ARIZONA STATE UNIV, DEPT BIOCHEM, TEMPE, AZ 85287 USA
[2] ARIZONA STATE UNIV, DEPT MICROBIOL, TEMPE, AZ 85287 USA
[3] MICROPROBE CORP, BOTHELL, WA 98021 USA
来源
关键词
D O I
10.1080/07391102.1992.10508670
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A procedure for imaging long DNA and double stranded RNA (dsRNA) molecules using Atomic Force Microscopy (AFM) is described. Stable binding of double stranded DNA molecules to the flat mica surface is achieved by chemical modification of freshly cleaved mica under mild conditions with 3-aminopropyltriethoxy silane. We have obtained striking images of intact lambda DNA, Hind III restriction fragments of lambda DNA and dsRNA from reovirus. These images are stable under repeated scanning and measured contour lengths are accurate to within a few percent. This procedure leads to strong DNA attachment, allowing imaging under water. The widths of the DNA images lie in the range of 20 to 80nm for data obtained in air with commercially available probes. The work demonstrates that AFM is now a routine tool for simple measurements such as a length distribution. Improvement of substrate and sample preparation methods are needed to achieve yet higher resolution.
引用
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页码:589 / 606
页数:18
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