Method for orienting DNA molecules on mica surfaces in one direction for atomic force microscopy imaging

被引:7
作者
Gad, M
Machida, M
Mizutani, W
Ishikawa, M
机构
[1] AIST, Angstrom Tech Partnership, Joint Res Ctr Atom Technol, Tsukuba, Ibaraki 3050046, Japan
[2] AIST, Natl Inst Biosci & Human Technol, Tsukuba, Ibaraki 3058566, Japan
关键词
D O I
10.1080/07391102.2001.10506755
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
An efficient method was developed to stretch DNA molecules on an atomically flat surface for AFM imaging. This method involves anchoring DNA molecules from their 5' ends to amino silanized mica surfaces, N-Succinimidyl6-[3'-(2-pyridyldithio) propionamido]hexanoate (LC-SPDP), a heterobifunctional cross-linker with a flexible spacer arm was used for this purpose. Immobilization was carried out by introducing a thiol group to the 5' end of DNA by PCR. Thiolated molecules were then reacted with the cross linker to conjugate with its 2-pyridyl disulphide group via sulfhydryl exchange. The resulting complex was deposited on amino silanized mica where NHS-ester moiety of the cross link-or reacted with the primary amino group on the surface. Samples were washed by a current of water and dried by an air jet in one direction parallel to the surface. DNA molecules were fully stretched in one direction on imaging them by AFM.
引用
收藏
页码:471 / 477
页数:7
相关论文
共 23 条
[11]   ATOMIC FORCE MICROSCOPY OF REOVIRUS DSRNA - A ROUTINE TECHNIQUE FOR LENGTH MEASUREMENTS [J].
LYUBCHENKO, YL ;
JACOBS, BL ;
LINDSAY, SM .
NUCLEIC ACIDS RESEARCH, 1992, 20 (15) :3983-3986
[12]   Structure, force, and energy of a double-stranded DNA oligonucleotide under tensile loads [J].
MacKerell, AD ;
Lee, GU .
EUROPEAN BIOPHYSICS JOURNAL WITH BIOPHYSICS LETTERS, 1999, 28 (05) :415-426
[13]   Atomic force microscopy imaging of DNA covalently immobilized on a functionalized mica substrate [J].
Shlyakhtenko, LS ;
Gall, AA ;
Weimer, JJ ;
Hawn, DD ;
Lyubchenko, YL .
BIOPHYSICAL JOURNAL, 1999, 77 (01) :568-576
[14]   A sensitive and rapid method for mapping protein bound to DNA by atomic force microscopy [J].
Tanigawa, M ;
Machida, M ;
Okada, T .
BIOSCIENCE BIOTECHNOLOGY AND BIOCHEMISTRY, 1997, 61 (10) :1751-1753
[15]  
Tanigawa M, 2000, Nucleic Acids Res, V28, pE38, DOI 10.1093/nar/28.9.e38
[16]   STRETCHED DNA STRUCTURES OBSERVED WITH ATOMIC-FORCE MICROSCOPY [J].
THUNDAT, T ;
ALLISON, DP ;
WARMACK, RJ .
NUCLEIC ACIDS RESEARCH, 1994, 22 (20) :4224-4228
[17]   PHYSICAL STUDIES OF PROTEIN-DNA COMPLEXES BY FOOTPRINTING [J].
TULLIUS, TD .
ANNUAL REVIEW OF BIOPHYSICS AND BIOPHYSICAL CHEMISTRY, 1989, 18 :213-237
[18]   Atomic force microscopy observation of deoxyribonucleic acid stretched and anchored onto aluminum electrodes [J].
Ueda, M ;
Iwasaki, H ;
Kurosawa, O ;
Washizu, M .
JAPANESE JOURNAL OF APPLIED PHYSICS PART 1-REGULAR PAPERS SHORT NOTES & REVIEW PAPERS, 1999, 38 (4A) :2118-2119
[19]   APPLICATIONS OF ELECTROSTATIC STRETCH-AND-POSITIONING OF DNA [J].
WASHIZU, M ;
KUROSAWA, O ;
ARAI, I ;
SUZUKI, S ;
SHIMAMOTO, N .
IEEE TRANSACTIONS ON INDUSTRY APPLICATIONS, 1995, 31 (03) :447-456
[20]   ATOMIC FORCE MICROSCOPY OF DNA-MOLECULES [J].
YANG, J ;
TAKEYASU, K ;
SHAO, Z .
FEBS LETTERS, 1992, 301 (02) :173-176