Nanoscale resolution in the focal plane of an optical microscope.

نویسندگان

  • Volker Westphal
  • Stefan W Hell
چکیده

Utilizing single fluorescent molecules as probes, we prove the ability of a far-field microscope to attain spatial resolution down to 16 nm in the focal plane, corresponding to about 1/50 of the employed wavelength. The optical bandwidth expansion by nearly an order of magnitude is realized by a saturated depletion through stimulated emission of the molecular fluorescent state. We demonstrate that en route to the molecular scale, the resolving power increases with the square root of the saturation level, which constitutes a new law regarding the resolution of an emerging class of far-field light microscopes that are not limited by diffraction.

برای دانلود رایگان متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Measuring 0.1-nm motion in 1 ms in an optical microscope with differential back-focal-plane detection.

Back-focal-plane detection of micrometer-sized beads offers subnanometer resolution for single-molecule, optical trapping experiments. However, laser beam-pointing instability and mechanical drift of the microscope limit the resolution of optical-trapping experiments. By combining two infrared lasers with improved differential beam-pointing stability (< or = 0.05 microrad), we simultaneously me...

متن کامل

Applications of Confocal Laser Scanning Microscopy in Dentistry. Study of the changes of the post-extraction sites

The Confocal Laser Scanning Microscope (CLSM) is an optical microscope that includes a laser light as a light source and an electronic system which helps on image processing. It obtains high-resolution and extremely thin optical image sections, removing the interference caused by the light arriving from the different optical fields across the thickness of the sample, and focusing on a single pl...

متن کامل

Stimulated emission depletion (STED) nanoscopy of a fluorescent protein-labeled organelle inside a living cell.

We demonstrate far-field optical imaging with subdiffraction resolution of the endoplasmic reticulum (ER) in the interior of a living mammalian cell. The diffraction barrier is overcome by applying stimulated emission depletion (STED) on a yellow fluorescent protein tag. Imaging individual structural elements of the ER revealed a focal plane (x, y) resolution of <50 nm inside the living cell, c...

متن کامل

Nanoscopy of bacterial cells immobilized by holographic optical tweezers

Imaging non-adherent cells by super-resolution far-field fluorescence microscopy is currently not possible because of their rapid movement while in suspension. Holographic optical tweezers (HOTs) enable the ability to freely control the number and position of optical traps, thus facilitating the unrestricted manipulation of cells in a volume around the focal plane. Here we show that immobilizin...

متن کامل

S09-04 OMX, a new microscope platform for increased time and spatial resolution

Most biochemical compounds absorb light and suffer phototoxic degradation, which induces malfunction or death of a specimen. The situation is particularly dramatic in conventional and confocal fluorescence microscopy. Even though only a single plane is observed, the entire specimen is illuminated. Recording stacks of images along the optical z-axis thus illuminates the entire specimen once for ...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

عنوان ژورنال:
  • Physical review letters

دوره 94 14  شماره 

صفحات  -

تاریخ انتشار 2005