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

투과 전자 현미경 또는 TEM은 샘플의 내부 구조와 구성을 연구하는 데 사용됩니다.
이 기기는 전자빔을 방출하는 전자총으로 구성됩니다. 그런 다음 빔은 두 개 이상의 전자기 응축기 렌즈를 사용하여 샘플에 초점을 맞춥니다.
샘플을 통해 전달되는 전자는 대물 렌즈에 의해 수집되고 초점이 맞춰져 중간 이미지를 형성합니다. 이 이미지는 추가 중간 렌즈 및 프로젝터 렌즈에 의해 더욱 확대됩니다.
최종 이미지는 인광 스크린 또는 CCD 카메라와 같은 전자 감지 이미징 장치를 사용하여 캡처할 수 있습니다.
TEM은 샘플의 2차원 흑백 이미지를 형성합니다. 어두운 영역은 전자를 거의 또는 전혀 전달하지 않는 밀집된 영역을 나타냅니다. 대조적으로, 밝은 영역은 더 많은 전자가 전달되는 영역을 나타냅니다.
TEM은 샘플 조성을 분석하는 데에도 사용됩니다. 전자빔-시료 상호 작용은 시료에 존재하는 다양한 원소를 식별하고 정량화하는 데 사용할 수 있는 특징적인 X선을 생성합니다.

투과 전자 현미경

Transmission Electron Microscopy

1931년 물리학자 에른스트 루스카는 렌즈가 광학현미경에서 빛의 광선을 유도할 수 있는 것처럼 자기장이 전자빔의 방향을 지정할 수 있다는 생각을 바탕으로 전자현미경의 첫 번째 프로토타입을 개발했습니다. 이러한 발전은 전자현미경 분야의 발전으로 이어졌습니다. 투과전자현미경(TEM)에서 전자는 뜨거운 텅스텐 원소에 의해 생성되고 전자총의 전위차에 의해 가속되어 최대 400keV의 운동 에너지를 제공합니다. 전자총을 떠난 후 전자빔은 전자기 렌즈(집합 렌즈 시스템)에 의해 초점이 맞춰지고 표본을 통해 투과되어 관찰됩니다. 표본의 이미지는 전송된 전자빔으로부터 재구성됩니다. 확대된 이미지는 형광 스크린에서 직접 볼 수도 있고 디지털 카메라나 컴퓨터 모니터 등으로 전송하여 간접적으로 볼 수도 있습니다.

전자총, 렌즈, 표본 및 형광 스크린으로 구성된 전체 설정은 빔의 에너지 손실을 방지하기 위해 진공 챔버에 담겨 있습니다. TEM의 최신 고해상도 모델은 0.5Å 이상의 분해능과 5천만 배 이상의 배율을 가질 수 있습니다. 비교를 위해 광학 현미경으로 얻은 최고의 분해능은 현재 약 97 nm입니다.

TEM의 한계는 표본의 두께가 약 100 nm여야 하며 생물학적 표본의 경우 초박형 슬라이스를 위해 안정화하기 위해 화학적 "고정"과 관련된 특별한 준비가 필요하다는 것입니다. 한계를 극복하기 위해 극저온 TEM과 같은 TEM 기술의 여러 발전이 이루어져 아티팩트를 제거하고 표본 고정 및 탈수의 표본 손상 단계 없이 직접 표본 이미징이 가능해졌습니다.

이 텍스트는 다음에서 수정되었습니다 <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 년 물리학 자 에른스트 루스카 (Ernst Ruska)는 렌즈가 광선을 지시 할 수있는 것처럼 자기장이 전자 빔을 지시 할 수 있다는 아이디어를 바탕으로 ...

Education

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JoVE Core

Cell Biology

세포생물학

Unit 1

제1단원

Visualizing Cells, Tissues, and Molecules

세포, 조직 및 분자의 시각화

KEY TERMS AND CONCEPTS

주요 용어 및 개념

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

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How TEM Reveals Tiny Structures

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