Name: how tem reveals tiny structures
Uploaded: 2023-04-30T12:01:08.000Z
Duration: 1 min 15 s
Channel: JoVE

透過型電子顕微鏡(TEM)は、試料の内部構造と組成を研究するために使用されます。
この装置は、電子ビームを放出する電子銃で構成されています。次に、ビームは2つ以上の電磁コンデンサーレンズを使用してサンプルに集束されます。
試料を透過した電子は、対物レンズによって集められ、集束されて中間像が形成されます。この画像は、追加の中間レンズとプロジェクターレンズによってさらに拡大されます。
最終的な画像は、蓄光スクリーンやCCDカメラなどの電子感受性イメージングデバイスを使用してキャプチャできます。
TEMは、サンプルの2次元の白黒画像を形成します。暗い領域は、電子をほとんどまたはまったく伝送しない密集した領域を表します。対照的に、明るい領域は、より多くの電子が透過する領域を示します。
TEMは、サンプル組成の分析にも使用されます。電子ビームとサンプルの相互作用により、サンプル中に存在するさまざまな元素を同定および定量するために使用できる特性X線が生成されます。

透過電子顕微鏡法

Transmission Electron Microscopy

1931 年、物理学者エルンスト・ルスカは、光学顕微鏡でレンズが光線を方向付けるのと同じように、磁場が電子ビームを方向付けることができるという考えに基づいて、電子顕微鏡の最初のプロトタイプを開発しました。 この発展は電子顕微鏡分野の発展につながりました。 透過型電子顕微鏡 (TEM) では、電子は高温のタングステン要素によって生成され、電子銃内の電位差によって加速され、最大 400 keV の運動エネルギーが与えられます。 電子銃を射出した後、電子ビームは電磁レンズ (集光レンズのシステム) によって集束され、観察される試料サンプルを通過します。 透過した電子ビームからサンプルの画像が再構成されます。 拡大された画像は、蛍光スクリーン上で直接見ることも、デジタル カメラやコンピュータ モニタなどに送信することによって間接的に見ることもできます。

電子銃、レンズ、試料、蛍光スクリーンからなるセットアップ全体は、ビームからのエネルギー損失を防ぐために真空チャンバー内に密閉されています。 最新の TEM の高解像度モデルは、0.5 Å を超える分解能と 5,000 万倍を超える倍率を備えています。 比較のために、現在光学顕微鏡で得られる最高の分解能は約 97 nm です。

TEM の制限として、サンプルの厚さは約 100 nm でなければならず、生体サンプルでは極薄スライス用にサンプルを安定させるために化学的「固定」を含む特別な準備が必要です。 この制限を克服するために、クライオ TEM などの TEM 技術のいくつかの進歩により、アーチファクトが除去され、サンプルの固定や脱水といったサンプルに損傷を与える段階を経ずにサンプルを直接イメージングできるようになりました。

このテキストは <a href="https://openstax.org/books/university-physics-volume-3/pages/6-6-wave-particle-duality?query=transmission%20electron&target=%7B%22type%22%3A%22search%22%2C%22index%22%3A0%7D#fs-id1163711954948">Openstax, University Physics Volume 3, Chapter 6 Photons and Matter Waves, Section 6.6: Wave-Particle Duality.</a>

1931年、物理学者エルンスト・ルスカは、レンズが光線を電子ビームに向けることができるのと同じように、磁場が電子ビームを向けることができるという考えに基づいています...

Education

JoVE Core

Cell Biology

細胞生物学

Unit 1

ユニット1

Visualizing Cells, Tissues, and Molecules

細胞・組織・分子の可視化

KEY TERMS AND CONCEPTS

主要用語と概念

how tem reveals tiny structures

Transmission electron microscopy uses electrons to reveal very small structures inside a specimen. The technique grew from the first electron microscope prototype developed in 1931 by physicist Ernst Ruska. He built on the idea that magnetic fields can direct an electron beam, just as lenses direct light in an optical microscope.

In a transmission electron microscope, a hot tungsten element produces electrons. An electron gun then accelerates them with a potential difference, giving the beam up to 400 keV of kinetic energy. Electromagnetic lenses, arranged as condensing lenses, focus the beam before it passes through the sample.

The image is formed from the electrons that move through the specimen. That reconstructed image can be viewed on a fluorescent screen or sent to a digital camera or computer monitor. The full system, including the electron gun, lenses, specimen, and screen, sits inside a vacuum chamber to reduce energy loss from the beam.

Modern high-resolution TEM models can resolve details smaller than 0.5 Å and reach magnifications above 50 million times. By comparison, the best resolving power of light microscopy is about 97 nm. TEM does have limits, because samples must be about 100 nm thick, and biological samples need chemical fixing before ultrathin slicing.

To reduce these limits, researchers have developed newer TEM methods such as cryo-TEM. These approaches help remove artifacts and can allow direct imaging without the sample-damaging steps of fixation and dehydration.

How TEM Reveals Tiny Structures

imaging biological samples with optical microscopy

imaging-biological-samples-with-optical-microscopy

How Light Microscopes Bring Samples Into View

Optical microscopy uses light and lenses to make tiny biological samples visible. Antonie van Leeuwenhoek built the first compound optical microscope in the 17th century to view blood cells, bacteria, and yeast cells. In 1830, Joseph Jackson Lister developed an essentially modern light microscope. During the 20th century, microscopes gained better magnification and resolution. A sample is placed on a glass slide and clipped onto the stage, which is the flat platform of the microscope. The...

phase contrast and differential interference contrast microscopy

phase-contrast-and-differential-interference-contrast-microscopy

Microscope Contrast for Live, Unstained Cells

Phase-contrast and differential interference contrast microscopy help scientists see live cells without stains. Both methods boost contrast so thin, transparent structures become easier to study under the microscope. Phase-contrast microscopes use interference between light that passes straight through a cell and light that is refracted by cell parts. The microscope uses an annular stop in the condenser to make a hollow cone of light. The objective lens also contains a phase plate with a phase...

fixation and sectioning

Microscope Slide Prep and Staining

Microscope slide preparation includes wet mounts, fixation, and staining. These steps help make specimens easier to see under a light microscope. They also help preserve cells and highlight important structures. A wet mount is the simplest slide preparation. The specimen is placed in a drop of liquid on the slide. A liquid sample can be added directly with a dropper, and a solid sample, such as a skin scraping, can be placed on the slide before the liquid is added. The liquid is sometimes...

immunofluorescence microscopy

Fluorescent Antibody Staining in Cells

Fluorescent antibody staining uses a fluorescence microscope to make cells and microbes visible in bright colors against a dark background. The microscope works with fluorochromes, which are fluorescent dyes that absorb energy from a light source and then give off visible light. Some fluorochromes are natural, such as chlorophylls. Others are added to the specimen to improve contrast. Common examples of fluorochromes include Texas red and FITC. The method can also use nucleic acid dyes such as...

immunocytochemistry and immunohistochemistry

immunocytochemistry-and-immunohistochemistry

Antibody Staining in Cells and Tissues

Immunocytochemistry (ICC) and immunohistochemistry (IHC) use antibodies to detect specific proteins or antigens in samples. ICC focuses on individual cells, such as blood cells and stem cells. IHC is used for tissue samples. These methods were first published by Albert Coons in 1941, when they were used to detect pneumococcal antigen in mouse tissue sections from mice infected with Pneumococcus. Both techniques can produce either a colored signal or a fluorescent signal. Enzyme-conjugated...

confocal fluorescence microscopy

Confocal Microscopy for Sharp Cell Images

Confocal microscopy is an advanced imaging method used to capture sharp fluorescence images. Its main advantage is that it blocks out-of-focus light from the sample with pinholes. That helps produce high-resolution images with strong contrast. Unlike a standard optical microscope, a confocal microscope uses a focused laser beam to scan the sample surface at different z-planes. This makes it especially useful for thick specimens, such as biofilms. These samples can often be examined alive and...

protein dynamics in living cells

Fluorescent Methods for Protein Movement

Protein movement in living cells can be measured with fluorescence-based methods such as FRAP, FRET, and PET. These techniques help scientists track how proteins move, interact, and change distance inside the cell. Fluorescent recovery after photobleaching, or FRAP, measures protein movement rates within the cell. In this method, a small region is exposed to a strong laser beam. The beam permanently bleaches fluorophore-tagged proteins in that area. Over time, bleached proteins diffuse away...

total internal reflection fluorescence microscopy

total-internal-reflection-fluorescence-microscopy

Surface-Only Imaging with TIRF Microscopy

Total internal reflection fluorescence microscopy, or TIRF, is a microscope method used to view fluorophores near a solid surface with a higher refractive index, such as a glass coverslip. It is useful when scientists want to study signals close to the cell surface. TIRF works when light from a medium with a lower refractive index, such as air, hits the glass coverslip at a critical angle. Instead of entering the glass, the light undergoes total internal reflection. This reflection creates an...

atomic force microscopy

Atomic Force Microscopy for Surface Mapping

Atomic force microscopy is used to map the surface details of materials. It can examine ceramics, glass, polymers, and biological samples. The method gives far more resolution than an optical imaging system and produces three-dimensional surface profiles instead of flat 2D images. The probe is the key part of an AFM setup. It includes the cantilever and tip assembly, and it is also the part that is replaced most often. Constant contact with samples wears down the tip, so probe choice depends...

super-resolution fluorescence microscopy

Sharper Cell Images with Fluorescence Microscopy

Super-resolution fluorescence microscopy gives sharper images than standard fluorescence microscopy by reducing the point spread function, or PSF. The PSF is the light pattern from a point source that makes it look blurred. Because of this blur, each fluorescent spot appears larger than it really is. Nearby fluorophores can also overlap through their PSFs and make the image less clear. Several super-resolution methods have been developed to improve image detail. Photoactivated localization...

overview of electron microscopy

Electron Microscopy: TEM vs SEM

Electron microscopy uses electrons instead of visible light to make images with much higher detail than a light microscope. Visible light limits the resolution of light microscopes, which usually magnify up to 1000X, and sometimes up to 1500X. Electrons have a much shorter wavelength, about 0.005 nm, so they can produce resolution as fine as 0.05 nm. An electron microscope can also magnify images up to 2,000,000X and reveal subcellular structures and some molecular structures, including single...

scanning electron microscopy

How SEM Reveals Surface Details

A scanning electron microscope (SEM) reveals the surface details of a sample with an electron beam. The beam scans across the sample in a two-dimensional pattern. SEM can image areas from about 1 centimeter down to 5 micrometers wide. SEM is useful for studying bacteria, viruses, tissues, and larger samples such as insects. Conventional SEM can produce magnification from 20X to 30,000X. It also offers spatial resolution of about 50 to 100 nanometers. The process starts when the electron gun...

transmission electron microscopy

Transmission electron microscopy uses electrons to reveal very small structures inside a specimen. The technique grew from the first electron microscope prototype developed in 1931 by physicist Ernst Ruska. He built on the idea that magnetic fields can direct an electron beam, just as lenses direct light in an optical microscope. In a transmission electron microscope, a hot tungsten element produces electrons. An electron gun then accelerates them with a potential difference, giving the beam...

preparation of samples for electron microscopy

preparation-of-samples-for-electron-microscopy

Electron Microscopy Sample Prep Methods

Electron microscopy sample prep methods help biological samples survive imaging in TEM and SEM. Before a specimen can be viewed, it must be fixed, or stabilized, so the electron beam does not damage it. It also must be dried well, or desiccated, because the microscope uses a vacuum. Fixation should happen as quickly as possible. Once a sample leaves its natural environment, its properties begin to change. In tissue samples, oxygen levels can drop and change the appearance of mitochondria. That...

immunogold electron microscopy

Immunogold Labeling in Electron Microscopy

Immunogold labeling in electron microscopy uses antibodies and tiny gold particles to find specific proteins in cells and tissues. The gold particles are very electron-dense, which means they show up clearly in electron microscope images. This gives researchers a high-resolution way to see where proteins are located and to compare their amounts under different stimulation conditions. The method can reveal proteins on the cell surface and inside cells. It has been used to study proteins...

cryo-electron microscopy

Cryo-EM for Native Biomolecule Imaging

Cryo-EM, or cryo-electron microscopy, lets scientists image biomolecules in their frozen, native state. It avoids the dehydration, fixation, and staining used in conventional electron microscopy, which can distort samples and create artifacts. It also reduces damage from the electron beam by using gentler imaging conditions. This method is useful when other structure tools have limits. X-ray diffraction needs a molecule to form a crystal, and that is not always possible. Even when...

electron microscope tomography and single-particle reconstruction

electron-microscope-tomography-and-single-particle-reconstruction

3D Imaging with Electron Microscopy

Transmission electron microscopy (TEM) can build 3D images of biological samples. It does this with electron microscope tomography and single-particle reconstruction. Tomography can show cell parts or small cells in vivo, while single-particle reconstruction is used for macromolecules and macromolecular complexes in vitro only. Electron tomography can be done in TEM or in STEM, which stands for scanning transmission electron microscopy. STEM is mainly used for thick biological specimens. It...

key terms and concepts

Learn how transmission electron microscopy uses electrons, magnetic lenses, and a vacuum to image ultra-thin samples at extreme magnification.

How TEM Reveals Tiny Structures | JoVE K12

cell biology

JoVE Core 細胞生物学は、複雑な細胞プロセスを、わかりやすく包括的なアニメーション ビデオ レッスンで説明します。このコレクションは、細胞小器官や膜、細胞輸送、細胞のエネルギー学など、細胞の必須コンポーネントと機能に焦点を当てています。これは、実際の研究実験における細胞生物学の応用を実証する科学者による実際のビデオによって補足されています。

How TEM Reveals Tiny Structures

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