Dyeing fungi: amphotericin B based fluorescent probes for multiplexed imaging

Assel Baibek; Muhammed Üçüncü; Bryn Short; Gordon Ramage; Annamaria Lilienkampf; Mark Bradley

doi:10.1039/d0cc08177a

Dyeing fungi: amphotericin B based fluorescent probes for multiplexed imaging

Chemical Communications ◽

10.1039/d0cc08177a ◽

2021 ◽

Vol 57 (15) ◽

pp. 1899-1902

Author(s):

Assel Baibek ◽

Muhammed Üçüncü ◽

Bryn Short ◽

Gordon Ramage ◽

Annamaria Lilienkampf ◽

...

Keyword(s):

Amphotericin B ◽

Fluorescent Probes ◽

Multiplexed Imaging

The clinically used antifungal polyene amphotericin B was conjugated, via the mycosamine and the aglycon moieties, to fluorophores.

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Application of fluorescent probes to study structural changes in Aspergillus fumigatus exposed to amphotericin B, itraconazole, and voriconazole

Mycopathologia ◽

10.1007/s11046-006-0040-y ◽

2006 ◽

Vol 162 (2) ◽

pp. 103-109 ◽

Cited By ~ 3

Author(s):

Madhurama Gangwar ◽

Richard Cole ◽

Rama Ramani ◽

Daniel J. Sheehan ◽

Vishnu Chaturvedi

Keyword(s):

Aspergillus Fumigatus ◽

Amphotericin B ◽

Fluorescent Probes ◽

Structural Changes

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Use of Fluorescent Probes To Determine MICs of Amphotericin B and Caspofungin against Candida spp. and Aspergillus spp.

Journal of Clinical Microbiology ◽

10.1128/jcm.43.8.3788-3792.2005 ◽

2005 ◽

Vol 43 (8) ◽

pp. 3788-3792 ◽

Cited By ~ 9

Author(s):

J. Peter ◽

D. Armstrong ◽

C. A. Lyman ◽

T. J. Walsh

Keyword(s):

Amphotericin B ◽

Fluorescent Probes ◽

Candida Spp

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Confocal microscopy of the cytoskeleton in living plant cells following microinjection of fluorescent probes

Proceedings, annual meeting, Electron Microscopy Society of America ◽

10.1017/s0424820100146497 ◽

1993 ◽

Vol 51 ◽

pp. 130-131

Author(s):

Ann Cleary

Keyword(s):

Cell Division ◽

Fluorescent Probes ◽

Actin Filaments ◽

Intracellular Transport ◽

Cell Structure ◽

Plant Cells ◽

Cell Plate ◽

Cell Cortex ◽

Living Plant ◽

Rhodamine Phalloidin

Microinjection of fluorescent probes into living plant cells reveals new aspects of cell structure and function. Microtubules and actin filaments are dynamic components of the cytoskeleton and are involved in cell growth, division and intracellular transport. To date, cytoskeletal probes used in microinjection studies have included rhodamine-phalloidin for labelling actin filaments and fluorescently labelled animal tubulin for incorporation into microtubules. From a recent study of Tradescantia stamen hair cells it appears that actin may have a role in defining the plane of cell division. Unlike microtubules, actin is present in the cell cortex and delimits the division site throughout mitosis. Herein, I shall describe actin, its arrangement and putative role in cell plate placement, in another material, living cells of Tradescantia leaf epidermis.The epidermis is peeled from the abaxial surface of young leaves usually without disruption to cytoplasmic streaming or cell division. The peel is stuck to the base of a well slide using 0.1% polyethylenimine and bathed in a solution of 1% mannitol +/− 1 mM probenecid.

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Live Confocal Analysis of Fertilization and Early Development

Microscopy and Microanalysis ◽

10.1017/s1431927600031135 ◽

2001 ◽

Vol 7 (S2) ◽

pp. 1012-1013

Author(s):

Uyen Tram ◽

William Sullivan

Keyword(s):

Drosophila Melanogaster ◽

Embryonic Development ◽

Real Time ◽

Early Development ◽

Fluorescent Probes ◽

Primary Defect ◽

Fluorescent Analysis ◽

Dynamic Event ◽

Enormous Amount ◽

Fluorescent Studies

Embryonic development is a dynamic event and is best studied in live animals in real time. Much of our knowledge of the early events of embryogenesis, however, comes from immunofluourescent analysis of fixed embryos. While these studies provide an enormous amount of information about the organization of different structures during development, they can give only a static glimpse of a very dynamic event. More recently real-time fluorescent studies of living embryos have become much more routine and have given new insights to how different structures and organelles (chromosomes, centrosomes, cytoskeleton, etc.) are coordinately regulated. This is in large part due to the development of commercially available fluorescent probes, GFP technology, and newly developed sensitive fluorescent microscopes. For example, live confocal fluorescent analysis proved essential in determining the primary defect in mutations that disrupt early nuclear divisions in Drosophila melanogaster. For organisms in which GPF transgenics is not available, fluorescent probes that label DNA, microtubules, and actin are available for microinjection.

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