DIRECT MEASUREMENT OF HYDROGEN-BONDING IN DNA NUCLEOTIDE BASES BY ATOMIC-FORCE MICROSCOPY

被引:214
作者
BOLAND, T
RATNER, BD
机构
[1] UNIV WASHINGTON, CTR BIOENGN, SEATTLE, WA 98195 USA
[2] UNIV WASHINGTON, DEPT CHEM ENGN, SEATTLE, WA 98195 USA
关键词
D O I
10.1073/pnas.92.12.5297
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
We have used self-assembled purines and pyrimidines on planar gold surfaces and on gold-coated atomic force microscope (AFM) tips to directly probe intermolecular hydrogen bonds. Electron spectroscopy for chemical analysis (ESCA) and thermal programmed desorption (TPD) measurements of the molecular layers suggested mono-layer coverage and a desorption energy of about 25 kcal/mol. Experiments were performed under water, with all four DNA bases immobilized on AFM tips and flat surfaces. Directional hydrogen-bonding interaction between the tip molecules and the surface molecules could be measured only when opposite base-pair coatings were used. The directional interactions were inhibited by excess nucleotide base in solution. Nondirectional van der Waals forces were present in all other cases. Forces as low as two interacting base pairs have been measured. With coated AFM tips, surface chemistry-sensitive recognition atomic force microscopy can be performed.
引用
收藏
页码:5297 / 5301
页数:5
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