Detecting Endogenous Macromolecules Detecting Endogenous structures, cell marking, small molecules...

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tecting Endogenous Macromolecul Detecting Endogenous structures ll marking, small molecules tecting ‘Planted’ Reporters

Transcript of Detecting Endogenous Macromolecules Detecting Endogenous structures, cell marking, small molecules...

Page 1: Detecting Endogenous Macromolecules Detecting Endogenous structures, cell marking, small molecules Detecting ‘Planted’ Reporters.

Detecting Endogenous Macromolecules

Detecting Endogenous structures ,cell marking, small molecules

Detecting ‘Planted’ Reporters

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Detecting Endogenous MacromoleculesProteinNucleic acids (RNA, DNA)

Detecting Endogenous structures ,cell marking, small molecules

Detecting ‘Planted’ Reporters

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GREEN marks theposition of the protein fibronectin in this frog embryo

Section

HOW DO WE DO THIS?

RED marks nuclei

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MakingPolyclonals

serum + or - purif.

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MCB 6.2(‘0601’)

Monoclonals

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PAGE PolyAcrylimide Gel Elecrophoresis

MCB 3

Western or Immunoblot MCB 3.5 “3EIMMBLOT”

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Immunocytochemistry

Most common enzyme conjugates:

Alkaline phosphataseHorseradish Peroxidase

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Fluorescent microscopy

FITC secondary

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Anti-fibronectinThen FITC

Fluorescence, rather than a converted substrate, as secondary to

mark protein’s presence

RED, PI, nuclear

counterstain

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Principle of Confocal microscopy

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Confocal – What it offers

Regular ConfocalFluorescence microscopy

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Actin Gurken

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Hunchback Kruppel

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Immunogold

Immunogold

SO:

Immunofluorescence

Immunocytochemistry

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For protein: antibody-antigen

For nucleic acid: n.a. complementarity

Tracking specific macromolecules

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MCB 7.2PCR

Start here week2/3

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In situ hybridization with 35S RNA probes1 2 3 4

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In situ hybridization using radioactive probe- expose photographic emulsion

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In situ –Shh

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FGF8 in situ

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FISH

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Northern

Northern or SLOT-BLOT

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Detecting Endogenous MacromoleculesProteinNucleic acids (RNA, DNA)

Detecting Endogenous structures ,cell marking, small molecules

Detecting ‘Planted’ Reporters

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Detection endogenous RNAs (hybridization + . . .)

Northern - or dot/slot blotDevelopmental Northern or SLOT-BLOT

In Situ Hybridization

MicroarrayTiling Microarray

RNA seq.Single cell RNA seq.

RIBOSOME PROFILING- on way to proteome

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MICROARRAY ANALYSIS

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Array analysis: see animation from Griffiths

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Figure 4.16(1) Microarray Analysis of Those Genes Whose Expression in the Early Xenopus Embryo Is Caused by the Activin-Like Protein Nodal-Related 1

(Xnr1)

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Figure 4.16(2) Microarray Analysis of Those Genes Whose Expression in the Early Xenopus Embryo Is Caused by the Activin-Like Protein Nodal-Related 1

(Xnr1)

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Figure 4.15(1) Microarray Technique

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Figure 4.15(2) Microarray Technique

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Detection endogenous RNAs (hybridization + . . .)

Northern - or dot/slot blotDevelopmental Northern or SLOT-BLOT

In Situ Hybridization

MicroarrayTiling Microarray

RNA seq.Single cell RNA seq.

RIBOSOME PROFILING- on way to proteome

NGS (Next Generation Sequencing)

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Detecting Endogenous Macromolecules

Detecting Endogenous structures ,cell marking, small molecules

Detecting ‘Planted’ Reporters

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Other markers of cells ‘Staining’ cells to follow cells / lineagesMarkers for small moleculesMarkers for cell compartments

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Vital dye injection into cells to follow cell lineage

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Flourecent dye injection into cells to follow cell lineage

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Dye injection into cells to map neurites (here, axons from retinal neurons to tectum)

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Other markers of cells ‘Staining’ cells to follow cells / lineagesMarkers for small moleculesMarkers for cell compartments

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Hoescht-Dye (or DAPI) Antibody, FITC to P granules

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A dye that fluoresces when it binds Ca++ Time series

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Detecting Endogenous Macromolecules

Detecting Endogenous structures ,cell marking, small molecules

Detecting ‘Planted’ Reporters To see protein, (OR RNA)

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MCB 5.1

ReporterConstructs

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Myf-5 Driven Beta-gal

X-gal

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Retinal-specific gene’s promoter driving GFP

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Acrosin-GFP

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GFP spindleshttp://www.duke.edu/web/microlabs/endow/moviepage.html

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What about seeing RNA molecules in cell

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