No abstract

Rapid biosensing requires fast mass transport of the analyte to the surface of the sensing element. To optimize analysis times, both mass transport in solution and the geometry and size of the sensing element need to be considered. Small dielectric spheres, tens of microns in diameter, can act as label-free biosensors using whispering gallery mode (WGM) resonances. WGM resonances are sensitive to the effective refractive index, which changes upon analyte binding to recognition sites on functionalized resonators. The spherical geometry and tens of microns diameter of these resonators provides an efficient target for sensing while their compact size enables detection in limited volumes. Here, we explore conditions leading to rapid analyte detection using WGM resonators as label-free sensors in 10 μL sample droplets. Droplet evaporation leads to potentially useful convective mixing, but also limits the time over which analysis can be completed. We show that active droplet mixing combined with initial binding rate measurements is required for accurate nanomolar protein quantification within the first minute following injection.

Scanning resonator microscopy (SRM) is developed to integrate whispering gallery mode (WGM) sensing with atomic force microscopy (AFM). The hybrid technique combines the exquisite refractive index sensing of whispering gallery mode resonators with the topography mapping capabilities of AFM. A 45 μm diameter barium titanate microsphere is attached to the end of a conventional AFM cantilever and acts as both a WGM resonator and stylus for mapping surface topography. Calibration plots, taken in contact-mode feedback, show that the WGM spectrum responds to changes in both solution and substrate refractive index. SRM imaging of a glass substrate reveals changes in surface refractive index that correspond to a small, 36 nm high feature measured simultaneously in the contact-mode topography image. Spectral measurements confirm that the contrast arises from refractive index changes and not coupling with sample topography, thus validating the approach. Additional measurements on thin polymer films and protein-coated surfaces are presented and discussed in terms of possible areas of application for SRM.

The desire to directly probe biological structures on the length scales that they exist has driven the steady development of various high-resolution microscopy techniques. Among these, optical microscopy and, in particular, fluorescence-based approaches continue to occupy dominant roles in biological studies given their favorable attributes. Fluorescence microscopy is both sensitive and specific, is generally noninvasive toward biological samples, has excellent temporal resolution for dynamic studies, and is relatively inexpensive. Light-based microscopies can also exploit a myriad of contrast mechanisms based on spectroscopic signatures, energy transfer, polarization, and lifetimes to further enhance the specificity or information content of a measurement. Historically, however, spatial resolution has been limited to approximately half the wavelength due to the diffraction of light. Near-field scanning optical microscopy (NSOM) is one of several optical approaches currently being developed that combines the favorable attributes of fluorescence microscopy with superior spatial resolution. NSOM is particularly well suited for studies of both model and biological membranes and application to these systems is discussed.