Label - free nanoscopy of living cells

نویسنده

  • Kenji Tsujino
چکیده

probability of this quantum receiver did not fall below 10–4 is due to experimental limitations; in particular, the visibility of the interferometer at the beamsplitter used in the displacement operation and the detection efficiency of the singlephoton detector were major sources of imperfection. Imperfect visibility causes errors in photon counts even when a correct displacement operation is carried out, and imperfect detection efficiency causes false negatives in photon counting for some signals displaced into the nonvacuum state. Nevertheless, by employing forward error correction methods used in conventional communication systems, the error rate of 10–4 can be reduced to a nearly error-free state. This suggests some challenges for the future, including the construction of a local oscillator required for the displacement operation. Of course, other improvements may also be needed, such as speeding up the operation of the required feedback loops and field-programmable gate array technology, downsizing the size and mass of the receiver, and developing faster single-photon detectors. Moreover, if this experiment is to be conducted outside of a laboratory environment, errors caused by background light must be taken into account. ❒ Kenji Tsujino is at the Department of Physics, Tokyo Women’s Medical University, 8-1 Kawada-cho, Shinjuku-ku, Tokyo 162-8666, Japan. e-mail: [email protected]

برای دانلود 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

Dual-label STED nanoscopy of living cells using photochromism.

We demonstrate live-cell STED microscopy of two protein species using photochromic green fluorescent proteins as markers. The reversible photoswitching of two markers is implemented so that they can be discerned with a single excitation and STED wavelength and a single detection channel. Dual-label STED microscopy is shown in living mammalian cells.

متن کامل

Two-Color 810 nm STED Nanoscopy of Living Cells with Endogenous SNAP-Tagged Fusion Proteins.

A 810 nm STED nanoscopy setup and an appropriate combination of two fluorescent dyes (Si-rhodamine 680SiR and carbopyronine 610CP) have been developed for near-IR live-cell super-resolution imaging. Vimentin endogenously tagged using the CRISPR/Cas9 approach with the SNAP tag, together with a noncovalent tubulin label, provided reliable and cell-to-cell reproducible dual-color confocal and STED...

متن کامل

RESOLFT nanoscopy with photoswitchable organic fluorophores

Far-field optical nanoscopy has been widely used to image small objects with sub-diffraction-limit spatial resolution. Particularly, reversible saturable optical fluorescence transition (RESOLFT) nanoscopy with photoswitchable fluorescent proteins is a powerful method for super-resolution imaging of living cells with low light intensity. Here we demonstrate for the first time the implementation...

متن کامل

Label-free photoacoustic nanoscopy.

Super-resolution microscopy techniques - capable of overcoming the diffraction limit of light - have opened new opportunities to explore subcellular structures and dynamics not resolvable in conventional far-field microscopy. However, relying on staining with exogenous fluorescent markers, these techniques can sometimes introduce undesired artifacts to the image, mainly due to large tagging age...

متن کامل

Far-field autofluorescence nanoscopy.

We demonstrate far-field optical imaging at the nanoscale with unlabeled samples. Subdiffraction resolution images of autofluorescent samples are obtained by depleting the ground state of natural fluorophores by transferring them to a metastable dark state and simultaneously localizing those fluorophores that are transiently returning. Our approach is based on the insight that nanoscopy methods...

متن کامل

Stimulated emission depletion nanoscopy of living cells using SNAP-tag fusion proteins.

We show far-field fluorescence nanoscopy of different structural elements labeled with an organic dye within living mammalian cells. The diffraction barrier limiting far-field light microscopy is outperformed by using stimulated emission depletion. We used the tagging protein hAGT (SNAP-tag), which covalently binds benzylguanine-substituted organic dyes, for labeling. Tetramethylrhodamine was u...

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

برای دانلود 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

عنوان ژورنال:

دوره   شماره 

صفحات  -

تاریخ انتشار 2013