Lecture 4 Reading Chapter 9 visualizing cells Flashcards Preview

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Flashcards in Lecture 4 Reading Chapter 9 visualizing cells Deck (61):
1

Scope of light microscope

0.4-0.7 micrometers

2

Optical diffraction effects

Light waves travel through different routes, and not in a straight line, so they interfere with each other

3

In phase

Interference makes things brighter

4

Out of phase

Light waves interfere with each other in such a way as to cancel each other partly or entirely

5

Micrometer

10^-6 m

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Nanometer

10^-9 meters

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Angstrom

10^-10 meters

8

Limit of resolution

The limiting separation at which two objects appear distinct. Depends on wavelength of light and numerical aperture of lens system used.

9

How does numerical aperture work

Affects the light gathering ability of the lens and is related both to the angle of the cone of light that can enter it and to the refractive index of the medium the lens is operating I

10

Refractive index

Ratio of the speed of light in a vacuum to the speed of light in a particular transparent medium

11

How can contrast in a specimen be generated

Light microscopes with special optical systems

12

Bright field microscope

Light passing through a cell in culture forms the image directly

13

Dark field microscopy

Exploits the fact that light rays can be scattered in all directions by small objects in their path. Bright image against a black background

14

How does light change as it passes through a cell

The phase of the light wave is changed according to the cell's refractive index.

15

How do phase contrast microscope and differential interference contrast microscope work

Increase phase differences caused by cell's refractive index so that waves are more nearly out of phase, producing amplitude differences when the sets of waves recombine, thereby creating an image of the cell's structure

16

How do we increase our ability to observe cells

We can attach a sensitive digital camera to a microscope, the camera detects light by means of charged coupled devices(CCDs) or high sensitivity complementary metal-oxide semiconductors (CMOs) sensors. These sensors are ten times more sensitive than naked human eye and can detect 100 times more intensity levels

17

How do we prepare tissue for microscopy

Fix and section tissue, then freeze or embed

18

Sections

Very thin transparent slices

19

Fixative

Forms covalent bonds with the free amino groups of proteins, cross linking the, so that they are stabilized and locked in position

20

Usual embedding medium for tissue

Waxes or resins

21

Three main approaches to working with thin tissue sections that reveal differences in types of molecules that are present

Sections can be stained with organic dyesthat have some specific affinity for particular subcellular components
Sectioned tissues can be used to visualize specific patterns of differential gene expression
Using fluorescent probes and markers

22

How do fluorescent molecules absorb and emit light

Absorb light at one wavelength and emit it at a longer wavelength.

23

Fluorescence microscope

Tool to visualize fluorescent dyes for staining cells. Illuminating light is passed through two sets of filters. One to filter the light before it reaches the specimen and one to filter the light obtained from the specimen,

24

When is fluorescence microscopy used

Ro detect specific proteins or other molecules in cells and tissues

25

How are antibodies used with fluorescent dyes

They are coupled. The. Antibody molecules serve as highly specific and versatile staining reagents that bind selectively to the particular macromolecules they recognize in cells or in the extracellular matrix.

26

What two dyes are used with antibodies frequently

Fluorescein , emits intense green fluorescence when excited with blue light
Rhodamine, emits deep red fluorescence when excited with green-yellow light

27

Quantum dots

Tiny crystals of semiconductor metal that can be excited to fluoresce by a broad spectrum of blue light

28

How are antibodies prepared for microscopy

Either purified from antiserum so as to remove all nonspecific antibodies, or they are specific monoclonal antibodies that only recognize the target molecule

29

Indirect immunocytochemistry

Using an unlabeled primary antibody and then detecting it with a group of labeled secondary antibodies that bind to it

30

Two ways to solve out of focus problem

Give many sectional views of optical sections
Image deconvolution

31

Image deconvolution

Computer calculates what blurring would have done and reverses

32

Point spread function

Blurred image of a point source

33

Confocal microscope

Manipulates light before it is measures. Analog technique.
Generally used with fluorescent optics. Focused on single point not ph whole object

34

Thick specimens are viewed with

Multi photon microscopes, with two-photon effect.

35

Green fluorescent protein (GFP)

Isolated from a jellyfish. Encoded by a single that can be cloned and introduced into cells of other species

36

How is GFP used usually

As a reporter molecule, a fluorescent probe to monitor gene expression

37

How do we use fluorescent proteins to uncover kinetic properties of a cell

Fluorescence resonance energy transfer (FRET)
Photoactivation
Fluorescence recovery after photo bleaching (FRAP)

38

FRET

Teo molecules of interest are each labeled with a different fluorochrome, chosen so that the emission spectrum of one fluorochrome, the donor, overlaps with the absorption spectrum of the other, the acceptor.

39

Photoactivation

Fluorescence tagging technique that allows detailed observations of proteins within cells. Involves synthesizing an inactive form of the fluorescent molecule of interest, introducing it into the cell, and then activating it suddenly at a chosen site in the cell by focusing a spot light on it.

40

Caged molecules

Inactive photosensitive precursors

41

Fluorescence recovery after photo bleaching (FRAP)

One uses a strong beam of light from a laser to extinguish the GFP fluorescence in a specified region of the cell, after which one can analyze the way in which remaining unbleached fluorescent protein molecules move into the bleached area as a function of time.

42

Why are micro electrodes not good at measuring changing ion concentrations

They reveal ion concentration only at one point of cell

43

Ion sensitive indicators

Suited to record rapid and transient changes in ion concentration. Have light emission that reflects local concentration of ion.

44

Aequorin

Luminescent protein. Emits blue light in presence of Ca2+, and responds to changes in concentration in the range of 0.5-10 micrometers.

45

Genetically encoded fluorescent indicators

Bind ion tightly. Are excited by or emit light at slightly different wavelengths when they are free of io than when bound. By measuring the ratio of fluorescence intensity at two excitation or emission wavelengths, one can determine concentration ratio of ion bound indicator to the free indicator and get a measurement of ion.

46

Why can't single fluorescent molecules be reliably detected in ordinary microscopes

Limitation arises from the strong background due to light emitted or scattered by out-of-focus molecules. This tends to blot out the fluorescence from the particular molecule of interest.

47

Total internal reflection fluorescence (TIRF) microscopy

Because of total internal reflection, light does not enter sample, so majority of fluorescent molecules are not illuminated. Electromagnetic energy does extend, as an evanescence field, for a short distance beyond the surface of the cover slip and into the specimen, allowing just those molecules in the layer closest to the surface to become excited.

48

Atomic force microscopy (AFM)

Provides a method to manipulate individual molecules. With its tip, probe can collect data on the variety of forces it encounters.

49

Approaches in light microscopy that bypass resolution imposed by diffraction of light. Superresolution approaches

Structured illumination microscopy (SIM)
Stimulated emission depletion microscopy (STED)
Photo activated localization microscopy (PALM)

50

Structured illumination microscopy SIM

Fluorescence imaging method with resolution of about 100 nm.uses grated or structured pattern of light to illuminate the sample. Illuminating grid and sample features combine into an interference pattern, from which the original high resolution contributions to the image beyond the classical resolution can be measures. Imaging is repeated several times and then combined mathematically to create an enhanced image.

51

Point spread function

Distribution of light intensity within the three dimensional, blurred image that is formed when a single point source of light is brought to a focus with a lens.

52

Stimulated emission depletion microscopy DTED

Increasing resolution by switching all the fluorescent molecules at the periphery of the blurry excitation spot back to their ground state, where they no longer fluoresce in their normal way. Diffraction limit breached because technique ensures that similar but very closely spaced molecules are in one of two different states, either fluorescing or dark.

53

Photo activated localization microscopy (PALM)

Labels are activated by illumination with near UV light. A small subset of molecules is modified so that they fluoresce when exposed to an excitation beam at another wavelength. These switch and another subset is activates. The photons of each subset given off are recorded and then aggregated into an image.

54

Preparing a specimen for electron microscopy

Living tissue is killed and preserved by fixation, usually with glutaraldehyde and osmium tetroxide, which binds to and stabilizes lipid bilayers as well as proteins. Cut into extremely thin sections.

55

What does image clarity depend on in an electron micrograph?

A range of contrasting electron densities. Impregnate tissues with salts of heavy metals.

56

Immunoglobulins electron microscopy

Incubate a thin section with a specific primary antibody, and then with a secondary antibody to which a colloidal gold particle has been attached.

57

Creating a third dimension view of a specimen

Have views of the same specimen from many different directions

58

Electron microscope tomography

Specimen holder is tilted to arrive at a 3d view

59

Scanning electron microscope (SEM)

Directly produces an image of the three dimensional structure of the surface of a specimen. Uses electrons that are scattered or emitted from the specimen's surface.

60

Negative staining

Allows finer detail of macromolecules to be seen. Molecules are supported on a thin film of carbon and mixed with a solution of heavy metal salt. Creates reverse or negative image of molecule.

61

Cell doctrine

All plants and animal tissues are aggregated of individual cells. Schleiden and Schwann, 1838