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We cant believe its already the end of the year! This year was filled with exciting new pro- spects in our unit and as always, we would like to share this with you before we end off this year. In this newsletter, we will share the open- ing of the CLEM platform that have been opti- mized in conjunction with the CAF EM unit. As always, we share some of the recent publica- tions from our users from mid-to-end 2016. We have some information on the new updates with regards to the first international ISAC workshop that we will be hosting in April 2017. As we are ending off the year, we do have a few announcements on the dates of the unit closure for 2016 and opening in 2017. Please feel free to contact us regarding projects in- volving microscopy and flow cytometry for the coming new year. We hope you enjoy the fes- tive season! On 11 October 2016, the CAF Fluorescence Microscopy Unit and the CAF Electron Mi- crobeam Unit hosted the Equipment Platform Launch of the Merlin FE SEM, Super- resolution microscopy and the new Correla- tive Light and Electron Microscopy (CLEM) platform. This event was met with great enthu- siasm. After a welcoming note from the director of CAF, Prof Gary Ste- vens, Mrs. Lize Engelbrecht and Dr Angelique Laurie showcased images and explained the tech- niques behind their work on super-resolution mi- croscopy, electron mi- croscopy and ultimately CLEM. Lastly, and most notably, Dr Lydia-Marie Joubert, electron micros- copy specialist from Stanford University, USA, presented on the applications of CLEM in her laboratory. She pro- vided great insight into CLEM and its many uses and drawbacks. Overall, the talks were well-received and we had a good response from the audience, with excitement for the newer platform in CAF. We would also like to thank Zeiss South Afri- ca for their sponsorship for the evening. WELCOME! CLEM PLATFORM LAUNCH IN THIS ISSUE WELCOME 1 CLEM PLATFORM LAUNCH 1 CLEM MICROSCOPY 2 RECENT ARTICLES 3 ISAC WORK- SHOP UPDATE 4 YEAR-END CLOSING 4 FLUORESCENCE MICROSCOPY UNIT ISSUE 11 NOV 2016 Mrs. Gail Giordani (from Zeiss), Dr Ben Loos, Mrs Lize Engelbrecht and Dr Angelique Coetzer Dr Lydia-Marie Joubert, Stanford Uni- versity

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Page 1: FLUORESCENCE MICROSCOPY UNIT WELCOMEblogs.sun.ac.za/fmc/files/2015/03/CAF-Imaging-Unit-Newsletter-issue-11.pdfMicroscopy Unit and the CAF Electron Mi-crobeam Unit hosted the Equipment

We cant believe its already the end of the year!

This year was filled with exciting new pro-

spects in our unit and as always, we would like

to share this with you before we end off this

year. In this newsletter, we will share the open-

ing of the CLEM platform that have been opti-

mized in conjunction with the CAF EM unit. As

always, we share some of the recent publica-

tions from our users from mid-to-end 2016. We

have some information on the new updates

with regards to the first international ISAC

workshop that we will be hosting in April 2017.

As we are ending off the year, we do have a

few announcements on the dates of the unit

closure for 2016 and opening in 2017. Please

feel free to contact us regarding projects in-

volving microscopy and flow cytometry for the

coming new year. We hope you enjoy the fes-

tive season!

On 11 October 2016, the CAF Fluorescence

Microscopy Unit and the CAF Electron Mi-

crobeam Unit hosted the Equipment Platform

Launch of the Merlin FE SEM, Super-

resolution microscopy and the new Correla-

tive Light and Electron Microscopy (CLEM)

platform.

This event

was met with

great enthu-

siasm. After

a welcoming

note from the

director of

CAF, Prof

Gary Ste-

vens, Mrs.

Lize Engelbrecht and Dr Angelique Laurie

showcased images and explained the tech-

niques behind their work

on super-resolution mi-

croscopy, electron mi-

croscopy and ultimately

CLEM. Lastly, and most

notably, Dr Lydia-Marie

Joubert, electron micros-

copy specialist from

Stanford University,

USA, presented on the

applications of CLEM in

her laboratory. She pro-

vided great insight into CLEM and its many

uses and drawbacks.

Overall, the talks were well-received and we

had a good response from the audience, with

excitement for the newer platform in CAF.

We would also like to thank Zeiss South Afri-

ca for their sponsorship for the evening.

WELCOME!

CLEM PLATFORM LAUNCH

IN THIS

ISSUE

WELCOME 1

CLEM PLATFORM

LAUNCH

1

CLEM

MICROSCOPY

2

RECENT ARTICLES 3

ISAC WORK-

SHOP UPDATE

4

YEAR-END

CLOSING

4

FLUORESCENCE MICROSCOPY UNIT I S S U E 1 1 N O V 2 0 1 6

Mrs. Gail Giordani (from Zeiss), Dr

Ben Loos, Mrs Lize Engelbrecht and

Dr Angelique Coetzer

Dr Lydia-Marie

Joubert, Stanford Uni-

versity

Page 2: FLUORESCENCE MICROSCOPY UNIT WELCOMEblogs.sun.ac.za/fmc/files/2015/03/CAF-Imaging-Unit-Newsletter-issue-11.pdfMicroscopy Unit and the CAF Electron Mi-crobeam Unit hosted the Equipment

P A G E 2

CORRELATIVE LIGHT AND ELECTRON MICROSCOPY C

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Below are some example images of CLEM that were presented at the launch.

a

a

a

b

b

b c

c

a b c

Persimmon fruit sections with imperfections: a) Transmitted light image, overlaid with autofluorescence

and b) a SEM image of the same area. The sample was later analysed for elemental content at the marked

locations.

a) Fluorescence image of a neuronal cell stained for the protein α–tubulin and a nuclear dye, b) a SEM image of

the same area, and c) the overlay of the fluorescence and electron micrographs.

Electrospun polymer fibres with antimicrobial coating. a) The fluorescence indicates the distribution of the antimicrobi-

al agent on the fibres, b) while the electron micrographs show morphology of the fibres. The Shuttle and Find feature of

the ZEN 2012 software (Zeiss) is then used to overlay these images.

Cancer cells treated with viral particles. a) Two cells stained with a membrane dye (green), a nuclear dye (blue) and

Cy3 labelled viral particles (red). b) A STEM image of a thin section (70 nm) through the same cells and c) an overlay

of the images.

Page 3: FLUORESCENCE MICROSCOPY UNIT WELCOMEblogs.sun.ac.za/fmc/files/2015/03/CAF-Imaging-Unit-Newsletter-issue-11.pdfMicroscopy Unit and the CAF Electron Mi-crobeam Unit hosted the Equipment

P A G E 3

RECENT ARTICLES C

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THE BRASSICACEAE SPECIES HELIOPHILA CORONOPIFOLIA PRODUCES ROOT BORDER-LIKE CELLS THAT PROTECT THE

ROOT TIP AND SECRETE DEFENSIN PEPTIDES

Root tip and detached border-like cells (BLCs)

stained with calcofluor white which stains cellu-

lose-enriched cell walls (A) and BLCs at higher

magnification (B). The appearance and formation

of border-like cells (BLCs) at the root tip of Heli-

ophila coronopifolia viewed under phase contrast

microscopy (C–E) are at 15-min intervals). The

arrows indicate attached BLCs. Scale bars: 40 um

(A),20 um (B), 200um (C-E)

Light microscopy observed cell

morphologies presented by B.

bruxellensis strains. Time 0 hours

(A) AWRI, (B) IWBT, (C) LO2E2;

Time 48 hours (D) AWRI, (E)

IWBT, (F) LO2E2; Time 72 hours

(G) AWRI, (H) IWBT, (I) LO2E2.

Florent Weiller, John P. Moore,*, Philip

Young, Azeddine Driouich and Melane´

A. Vivier. (2016)

ANNALS OF BOTANY

COMPARATIVE MORPHOLOGICAL CHARACTERISTICS OF THREE BRETTANOMYCES BRUXELLENSIS WINE STRAINS IN THE

PRESENCE/ABSENCE OF SULFUR DIOXIDE

Marli Louw, Maret du Toit, Her-

vé Alexandre, Benoit Divol

(2016)

INTERNATIONAL JOURNAL OF

FOOD MICROBIOLOGY , Volume

238, pp: 79–88

Page 4: FLUORESCENCE MICROSCOPY UNIT WELCOMEblogs.sun.ac.za/fmc/files/2015/03/CAF-Imaging-Unit-Newsletter-issue-11.pdfMicroscopy Unit and the CAF Electron Mi-crobeam Unit hosted the Equipment

P A G E 4

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As we are ending the year,

kindly note that the unit will be

closed as of the 16th Decem-

ber 2016 and we will reopen

on the 9th January 2017.

Please ensure that all your data has been col-

lected and backed up before going on holiday.

Limited assistance will be available in Decem-

ber, so please speak to us if you would like to

work in December so you can receive the

necessary training. Fully trained users also

have to make arrangements to work during

the holiday.

We wish you a great festive season and a

happy 2017!.

UNIT YEAR-END CLOSING

ISAC-BD FLOW CYTOMETRY WORKSHOP 2017

As we mentioned in our previous newsletter,

the CAF Fluorescence Microscopy Unit will be

hosting the first international ISAC-BD Flow

Cytometry Workshop from the 11th to 13th

April 2017. Several international flow cytome-

try experts will be conducting workshops

which will range from basic flow cytometry

principles to specialized techniques for stem

cell biology, cell proliferation and cell death

assays and multi-parameter analysis.

We are pleased to announce that the early-

bird registrations are now open and students

will be able to submit abstracts for poster

presentation.

For more information on the ISAC-BD work-

shop, please visit the website:

http://www.isac-capetown-flowworkshop.com/

or contact Lize Engelbrecht for more infor-

mation.

Tygerberg Flow Cytometry Centre:

Mrs. Andrea Gutschmidt ([email protected])

Tel: 021 938 9400 / 9786

Contact us:

Stellenbosch Main campus

Mrs. Lize Engelbrecht ([email protected])

Ms. Rozanne Adams ([email protected])

Ms. Dumisile Lumkwana ([email protected]) Tel: 021 808 9327 / 4030

REGISTRATION IS NOW OPEN

Booking system: http://www.supersaas.com/schedule/CAF_Fluorescent_Microscopy_Unit

Websites: www.sun.ac.za/caf OR blogs.sun.ac.za/fmc