Routine and Timely Sub-picoNewton Force Stability and Precision for Biological Applications of Atomic Force Microscopy

被引:54
作者
Churnside, Allison B. [1 ,2 ]
Sullan, Ruby May A. [1 ]
Nguyen, Duc M. [1 ,3 ]
Case, Sara O. [1 ]
Bull, Matthew S. [1 ,2 ]
King, Gavin M. [1 ]
Perkins, Thomas T. [1 ,4 ]
机构
[1] Natl Inst Stand & Technol, Joint Inst Lab Astrophys, Boulder, CO 80309 USA
[2] Univ Colorado, Dept Phys, Boulder, CO 80309 USA
[3] Univ Colorado, Dept Chem & Biol Engn, Boulder, CO 80309 USA
[4] Univ Colorado, Dept Mol Cellular & Dev Biol, Boulder, CO 80309 USA
基金
美国国家科学基金会;
关键词
Atomic force microscopy; scanning probe microscopy; single molecule force spectroscopy; drift; overstretching DNA; cantilever; DNA; CANTILEVERS; SPECTROSCOPY;
D O I
10.1021/nl301166w
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Force drift is a significant, yet unresolved, problem in atomic force 1 microscopy (AFM). We show that the primary source of force drift for a popular class of cantilevers is their gold coating, even though they are coated on both sides to minimize drift. Drift of the zero-force position of the cantilever was reduced from 900 nm for gold-coated cantilevers to 70 nm (N = 10; rms) for uncoated cantilevers over the first 2 h after wetting the tip; a majority of these uncoated cantilevers (60%) showed significantly less drift (12 nm, rms). Removing the gold also led to similar to 10-fold reduction in reflected light, yet short-term (0.1-10 s) force precision improved. Moreover, improved force precision did not require extended settling; most of the cantilevers tested (9 out of 15) achieved sub-pN force precision (0.54 +/- 0.02 pN) over a broad bandwidth (0.01-10 Hz) just 30 min after loading. Finally, this precision was maintained while stretching DNA. Hence, removing gold enables both routine and timely access to sub-pN force precision in liquid over extended periods (100 s). We expect that many current and future applications of AFM can immediately benefit from these improvements in force stability and precision.
引用
收藏
页码:3557 / 3561
页数:5
相关论文
共 31 条
[1]   Reducing probe dependent drift in atomic force microscope with symmetrically supported torsion levers [J].
Beyder, A ;
Spagnoli, C ;
Sachs, F .
REVIEW OF SCIENTIFIC INSTRUMENTS, 2006, 77 (05)
[2]   High-resolution atomic force microscopy and spectroscopy of native membrane proteins [J].
Bippes, Christian A. ;
Muller, Daniel J. .
REPORTS ON PROGRESS IN PHYSICS, 2011, 74 (08)
[3]   Ten years of tension: single-molecule DNA mechanics [J].
Bustamante, C ;
Bryant, Z ;
Smith, SB .
NATURE, 2003, 421 (6921) :423-427
[4]   Automated setpoint adjustment for biological contact mode atomic force microscopy imaging [J].
Casuso, Ignacio ;
Scheuring, Simon .
NANOTECHNOLOGY, 2010, 21 (03)
[5]   Direct observation of the three-state folding of a single protein molecule [J].
Cecconi, C ;
Shank, EA ;
Bustamante, C ;
Marqusee, S .
SCIENCE, 2005, 309 (5743) :2057-2060
[6]   Mechanical stability of single DNA molecules [J].
Clausen-Schaumann, H ;
Rief, M ;
Tolksdorf, C ;
Gaub, HE .
BIOPHYSICAL JOURNAL, 2000, 78 (04) :1997-2007
[7]   DNA: An extensible molecule [J].
Cluzel, P ;
Lebrun, A ;
Heller, C ;
Lavery, R ;
Viovy, JL ;
Chatenay, D ;
Caron, F .
SCIENCE, 1996, 271 (5250) :792-794
[8]   Protein adsorption on model surfaces with controlled nanotopography and chemistry [J].
Denis, FA ;
Hanarp, P ;
Sutherland, DS ;
Gold, J ;
Mustin, C ;
Rouxhet, PG ;
Dufrêne, YF .
LANGMUIR, 2002, 18 (03) :819-828
[9]   Force-clamp spectroscopy monitors the folding trajectory of a single protein [J].
Fernandez, JM ;
Li, HB .
SCIENCE, 2004, 303 (5664) :1674-1678
[10]   High-resolution, single-molecule measurements of biomolecular motion [J].
Greenleaf, William J. ;
Woodside, Michael T. ;
Block, Steven M. .
ANNUAL REVIEW OF BIOPHYSICS AND BIOMOLECULAR STRUCTURE, 2007, 36 :171-190