(Phys.org) —JILA researchers have engineered a short, flexible, reusable probe for the atomic force microscope (AFM) that enables state-of-the-art precision and stability in picoscale force measurements. Shorter, softer and more agile than standard and recently enhanced AFM probes, the JILA tips will benefit nanotechnology and studies of folding and stretching in biomolecules such as proteins and DNA.
An AFM probe is a cantilever, shaped like a tiny diving board with a small, atomic-scale point on the free end. To measure forces at the molecular scale in a liquid, the probe attaches its tip to a molecule such as a protein and pulls; the resulting deflection of the cantilever is measured. The forces are in the realm of piconewtons, or trillionths of a newton. One newton is roughly the weight of a small apple.
The new probe design, described in ACS Nano, is the JILA research group's third recent advance in AFM technology. JILA is jointly operated by the National Institute of Standards and Technology (NIST) and University of Colorado Boulder.
The group previously improved AFM position stability by using laser beams to sense motion and removing the gold coating from long probe tips, or cantilevers, to enhance long-term force stability. However, removing the gold reduces the strength of the signal being measured, and using long cantilevers leads to other measurement problems such as slower response to dynamic events like protein unfolding.
The latest modification overcomes these and other issues, improving precision without loss of stability, speed, or sensitivity. JILA researchers used a focused ion beam to cut a hole in the center of a short commercial cantilever and thinned the remaining support structures, thereby reducing the cantilever's stiffness and friction near surfaces. The result is excellent long-term stability and improved short-term precision, respectively, in AFM force measurements.
JILA researchers also added a protective glass cap over the gold coating at the end of the cantilever to retain beneficial reflectivity, and then removed the remaining gold to gain force stability. The modified cantilever enables rapid, precise and stable force measurements across a broad range of operating frequencies.
"Previously, we had to average the Brownian (random) motion of our favorite cantilever for about 60 milliseconds to get a measurement that had a precision of 1 piconewton," JILA/NIST biophysicist Tom Perkins says. "Now, we can get the same precision in 1 millisecond or so."
JILA researchers demonstrated significant benefits for single molecule studies. For instance, the short, soft cantilevers can quickly measure abrupt changes in force when a protein unfolds. Protein folding is required for proper biological function and misfolding can lead to diseases such as Alzheimer's. The new cantilevers match the response of stiffer, unmodified cantilevers but with greater stability and precision. Force stability is crucial in this application because protein folding and unfolding rates are exponentially sensitive to tiny changes (smaller than 1 piconewton) in applied load. The new device also can track fleeting nanoscale events, including protein folding, over hundreds of seconds—much longer periods than previously possible. The new design should also be applicable to rapid probing of the mechanical properties of materials at the nanoscale.
Significantly, the new cantilevers are robust enough to be reused for multiple days. Moreover, JILA researchers say the new design is simple and inexpensive to make, and thus, suitable for routine use.
"Amazingly, this project was spearheaded by a talented undergraduate. We hope other groups with similarly talented students will adopt these cantilevers. We certainly are," Perkins said.
Explore further: Making a Point: Picoscale Stability in a Room-Temperature AFM
M.S. Bull, R.M.A. Sullan, H. Li and T.T. Perkins. "Improved single-molecule force spectroscopy using micromachined cantilevers." ACS Nano. Published online March 26,2014. DOI: 10.1021/nn5010588