The researchers characterize their new technique as a neat solution to the "needle in a haystack" problem of nanoscale microscopy, but it's more like the difference between finding the coffee table in a darkened room either by walking around until you fall over it, or using a flashlight. In a new paper, a group from JILA - a joint venture of the National Institute of Standards and Technology (NIST) and the University of Colorado - finds tiny assemblies of biomolecules for subsequent detailed imaging by combining precision laser optics with atomic force microscopy.
The atomic force microscope (AFM) has become one of the standard tools of nanotechnology. The concept is deceptively simple. A needle - not unlike an old-fashioned phonograph stylus, but much smaller with a tip at most only a couple of atoms wide - moves across the surface of the specimen. A laser measures tiny deflections of the tip as it is pushed or pulled by atomic scale forces, such as electrostatic forces or chemical attraction. Scanning the tip back and forth across the sample yields a three-dimensional image of the surface. The resolution can be astonishing - in some cases showing individual atoms, a resolution a thousand times smaller than the best optical microscopes can achieve. Such amazing sensitivity incurs a technical problem: if the probe can image an object of, e.g. 100 nm2, how exactly does one find that object if it could be nearly anywhere on a microscope stage a million times that size? That's not an unusual case in biological applications. The brute-force answer is, one scans the probe back and forth, probably at a higher speed, until it runs into something interesting. Like the coffee table in the dark, this has problems. The AFM tip is not only very delicate and easy to damage, but it can be degraded by picking up unwanted atoms or molecules from the surface. Also, in the biosciences, where the AFM is becoming increasingly important, research specimens usually are "soft" things like proteins or membranes that can be damaged by an uncontrolled collision with the tip. One solution has been to "label" the target molecule with a small fluorescent compound or quantum dot, so that it lights up and is easy to find, but that means chemically altering the subject, which may not be desirable.
Instead, the JILA team opted to use a flashlight.
Building upon an earlier innovation for stabilizing the position of an AFM tip, the group uses a tightly focused, low-power laser beam to optically scan the area, identifying target locations by minute changes in the scattered light. This laser is scanned across the sample to form an image, analogous to forming an AFM image. The same laser - and detection technique - is used to locate the AFM tip. Hence, the laser serves as a common frame of reference and it's relatively straightforward to align the optical and the AFM image. In experiments with patches of cell membrane from single-cell organisms, the group has demonstrated that they can locate these protein complexes and align the AFM tip with a precision of about 40 nm. Relying solely on scattered light, their technique requires no prior chemical labeling or modification of the target molecules.
Churnside A.B. et al.: Label-free optical imaging of membrane patches for atomic force microscopy. Optics Express. Vol. 18, No. 23. Nov. 8, 2010.
Related Articles :