Arindam Ghosh, PhD's Avatar

Arindam Ghosh, PhD

@arindam92.bsky.social

Incoming Research Group Leader, DKFZ NCT WERA #Biophysics #Imaging #Immunology #Receptors

721 Followers  |  1,571 Following  |  26 Posts  |  Joined: 08.11.2024
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Posts by Arindam Ghosh, PhD (@arindam92.bsky.social)

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How genetically encoded sensors have lit up neuroscience Tools that track specific molecules in neurons have enabled researchers to probe previously unexplored aspects of neurobiology β€” although important caveats remain.

Got the last word in this great perspective on the state of fluorescent indicators in @nature.com by @dianakwon.bsky.social www.nature.com/articles/d41...

14.11.2025 15:12 β€” πŸ‘ 17    πŸ” 4    πŸ’¬ 0    πŸ“Œ 0

Thanks a lot, Luciano! Wishing you a great start as well.

12.11.2025 07:37 β€” πŸ‘ 1    πŸ” 0    πŸ’¬ 0    πŸ“Œ 0

Thanks so much for your kind wishes, Mike!

12.11.2025 07:36 β€” πŸ‘ 1    πŸ” 0    πŸ’¬ 0    πŸ“Œ 0

Thank you so much!

12.11.2025 07:35 β€” πŸ‘ 0    πŸ” 0    πŸ’¬ 0    πŸ“Œ 0

Thanks so much!

11.11.2025 17:12 β€” πŸ‘ 1    πŸ” 0    πŸ’¬ 0    πŸ“Œ 0

Thanks so much! Exciting times ahead!

11.11.2025 17:12 β€” πŸ‘ 0    πŸ” 0    πŸ’¬ 0    πŸ“Œ 0

Thank you so much for your kind wishes, Johannes! Let's stay in touch

11.11.2025 17:10 β€” πŸ‘ 1    πŸ” 0    πŸ’¬ 0    πŸ“Œ 0

Thanks a lot, Falk! Looking forward to exciting Collab in the future

11.11.2025 17:09 β€” πŸ‘ 1    πŸ” 0    πŸ’¬ 1    πŸ“Œ 0

Thanks so much, Biswajit

11.11.2025 17:07 β€” πŸ‘ 1    πŸ” 0    πŸ’¬ 0    πŸ“Œ 0

I am never under the misapprehension that my accomplishments are mine alone. To my parents and my partner, we had this journey together, and here we are today. Life has been rather kind that I have all of you. Looking forward to the years ahead!

11.11.2025 13:33 β€” πŸ‘ 4    πŸ” 0    πŸ’¬ 0    πŸ“Œ 0

I am grateful and would like to thank all my academic mentors till date, especially, my PhD supervisor JΓΆrg Enderlein @joergenderlein.bsky.social and postdoc mentor Markus Sauer @sauer-lab.bsky.social Thank you for the opportunity to work with you and putting trust in me.

11.11.2025 13:33 β€” πŸ‘ 6    πŸ” 0    πŸ’¬ 1    πŸ“Œ 0

Happy to share that I will be starting my independent research career as a Research Group Leader at the German Cancer Research Center (DKFZ). Starting from January 2026, my group will be based at DKFZ National Center for Tumor Diseases (NCT WERA), WΓΌrzburg, Germany.

11.11.2025 13:33 β€” πŸ‘ 31    πŸ” 2    πŸ’¬ 8    πŸ“Œ 1
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πŸ‘ Congratulation to the πŸ† winners of Student Award held by #PicoQuant during 30th anniversary of our annual workshop on Single Molecule Spectroscopy and Ultra Sensitive Analysis in the Life Sciences. #WS30
We were proud to once again support the next generation of scientists. #PicoQuantStudentAward

26.09.2025 11:12 β€” πŸ‘ 8    πŸ” 2    πŸ’¬ 0    πŸ“Œ 0
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🚨
New Preprint!
Ex-dSTORM resolves fine details of the molecular architecture of CCPs, the 8-nm periodicity of microtubules, and the docking site of synaptic vesicles at the presynapse of hippocampal neurons.

▢️ www.biorxiv.org/content/10.1...

19.08.2025 15:32 β€” πŸ‘ 50    πŸ” 20    πŸ’¬ 1    πŸ“Œ 0
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SNAP-tag2 for faster and brighter protein labeling - Nature Chemical Biology SNAP-tag is a widespread tool for labeling protein for bioimaging. Now, KΓΌhn et al. report SNAP-tag2 with increased labeling kinetics and brightness, which translates into a better performance in live...

Finally out in Nature Chem Bio:
SNAP-tag2 for faster and brighter protein labeling
www.nature.com/articles/s41...
Thank you Steffi and Veselin.

03.07.2025 19:45 β€” πŸ‘ 173    πŸ” 75    πŸ’¬ 2    πŸ“Œ 3
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Great news: I received ERC Advanced grant #ERCAdG @erc.europa.eu CaptuRel! It aims at intelligent nanomaterials undergoing bioinspired cycle of capture and photorelease of bioactive molecules for sensing and controlling (bio)chemical gradients. Thanks to my Team, @cnrs.fr and @unistra.fr!

17.06.2025 10:41 β€” πŸ‘ 48    πŸ” 4    πŸ’¬ 0    πŸ“Œ 1
Fig. 4 Super-resolution microscopy in live and fixed cells with Rhobin.
(A) Rhobin transiently binds rhodamine molecules and thereby constantly replenishes signal lost
through photobleaching of dyes. (B-D) No-wash STED microscopy of live U2OS cells transiently
expressing LifeAct-Rhobin2 labeled with 100 nM JFX650. (C, D) Zoom-ins of regions highlighted
in (B) imaged either with confocal or STED microscopy. Scale bar: 20 ΞΌm (B) and 10 ΞΌm (C, D).
(E-H) Rhobin enables timelapse STED microscopy of fast ER dynamics with minimal signal loss.
U2OS stably expressing N-terminal tag fusions of SEC61B were stained with 1 ΞΌM Halo-JFX650
(HaloTag7, reHaloF) or 2 ΞΌM SiRhP (Rhobin2) and imaged at a frame rate of 0.387 fps for at least
100 time points. (F, G) Selected frames from timelapse acquisitions of Rhobin2:SEC61B labeled
with SiRhP (F) or HaloTag7:SEC61B labeled with Halo-JFX650 (G). Scale bar: 2 ΞΌm. (H) Signal
.CC-BY-NC 4.0 International licenseavailable under a
(which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made
The copyright holder for this preprintthis version posted June 25, 2025.;https://doi.org/10.1101/2025.06.24.661379doi:bioRxiv preprint
22
loss during timelapse imaging. Mean Β± SD signal inside cells over time for indicated constructs.
(I-K) PAINT-type super-resolution microscopy with Rhobin. Rhobin2-SEC61B was transiently
expressed in U2OS cells and labeled with 5 nM SiRhP after chemical fixation. Imaging under no-
wash conditions and near-TIRF illumination. (I) Repeated, but transient binding of SiRhP
molecules to Rhobin2 at low nanomolar concentrations can be observed as intensity bursts in
intensity time traces extracted from a diffraction-limited area. See movie S3 for raw data of
binding-induced blinking. (J) Sum image across 10,000 frames of an image stack, simulating a
diffraction-limited image. (K). Reconstructed image from localized molecules in the full stack.

Fig. 4 Super-resolution microscopy in live and fixed cells with Rhobin. (A) Rhobin transiently binds rhodamine molecules and thereby constantly replenishes signal lost through photobleaching of dyes. (B-D) No-wash STED microscopy of live U2OS cells transiently expressing LifeAct-Rhobin2 labeled with 100 nM JFX650. (C, D) Zoom-ins of regions highlighted in (B) imaged either with confocal or STED microscopy. Scale bar: 20 ΞΌm (B) and 10 ΞΌm (C, D). (E-H) Rhobin enables timelapse STED microscopy of fast ER dynamics with minimal signal loss. U2OS stably expressing N-terminal tag fusions of SEC61B were stained with 1 ΞΌM Halo-JFX650 (HaloTag7, reHaloF) or 2 ΞΌM SiRhP (Rhobin2) and imaged at a frame rate of 0.387 fps for at least 100 time points. (F, G) Selected frames from timelapse acquisitions of Rhobin2:SEC61B labeled with SiRhP (F) or HaloTag7:SEC61B labeled with Halo-JFX650 (G). Scale bar: 2 ΞΌm. (H) Signal .CC-BY-NC 4.0 International licenseavailable under a (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made The copyright holder for this preprintthis version posted June 25, 2025.;https://doi.org/10.1101/2025.06.24.661379doi:bioRxiv preprint 22 loss during timelapse imaging. Mean Β± SD signal inside cells over time for indicated constructs. (I-K) PAINT-type super-resolution microscopy with Rhobin. Rhobin2-SEC61B was transiently expressed in U2OS cells and labeled with 5 nM SiRhP after chemical fixation. Imaging under no- wash conditions and near-TIRF illumination. (I) Repeated, but transient binding of SiRhP molecules to Rhobin2 at low nanomolar concentrations can be observed as intensity bursts in intensity time traces extracted from a diffraction-limited area. See movie S3 for raw data of binding-induced blinking. (J) Sum image across 10,000 frames of an image stack, simulating a diffraction-limited image. (K). Reconstructed image from localized molecules in the full stack.

De novo designed bright, hyperstable rhodamine binders for fluorescence microscopy by Bo Huang and team: www.biorxiv.org/content/10.1...

26.06.2025 13:50 β€” πŸ‘ 69    πŸ” 19    πŸ’¬ 1    πŸ“Œ 2
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🚨 New preprint!
Using U-ExM + in situ cryo-ET, we show how C2CD3 builds an in-to-out radial architecture connecting the distal centriole lumen to its appendages. Great collab with @cellarchlab.com @chgenoud.bsky.social @stearnslab.bsky.social πŸ™Œ. #TeamTomo #UExM
www.biorxiv.org/content/10.1...

19.06.2025 08:58 β€” πŸ‘ 119    πŸ” 46    πŸ’¬ 0    πŸ“Œ 2
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Plasma membrane labelling efficiency, internalization and partitioning of functionalized fluorescent lipids as a function of lipid structure Labeling the plasma membrane for advanced imaging remains a significant challenge. For time-lapse live cell imaging, probe internalization and photobleaching are major limitations affecting most membr...

New paper out! Would you like to fluorescently label the plasma membrane in live, fixed or permeabilized cells? I tested different lipid structures and labelling approaches to decide what makes a good membrane labelling probe for such imaging experiments!
www.biorxiv.org/content/10.1...

13.05.2025 12:07 β€” πŸ‘ 71    πŸ” 18    πŸ’¬ 3    πŸ“Œ 1

Very excited to present our latest work: SPINNA, an analysis framework and software package for single-protein resolution data! πŸ–₯️🀩

We can directly quantify stoichiometry and oligomerization from super-res (DNA-PAINT, RESI) images!! 🧬🎨

07.05.2025 14:56 β€” πŸ‘ 30    πŸ” 11    πŸ’¬ 0    πŸ“Œ 0
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One-click image reconstruction in single-molecule localization microscopy via deep learning Deep neural networks have led to significant advancements in microscopy image generation and analysis. In single-molecule localization based super-resolution microscopy, neural networks are capable of...

Collaborative work with the Shechtman Lab and @heilemannlab.bsky.social.

Check it out here: www.biorxiv.org/content/10.1...

22.04.2025 13:16 β€” πŸ‘ 9    πŸ” 4    πŸ’¬ 0    πŸ“Œ 0
Open-source Sub-Nanometer Stabilization System for Super-resolution Fluorescence Microscopy Recent advances in fluorescence nanoscopy have pushed resolution to the 1-10 nm range, enabling the direct visualization of individual molecules even in crowded biological environments. Achieving this...

www.researchsquare.com/article/rs-6...

22.04.2025 10:47 β€” πŸ‘ 1    πŸ” 0    πŸ’¬ 0    πŸ“Œ 0

Thanks so much!

01.04.2025 23:54 β€” πŸ‘ 0    πŸ” 0    πŸ’¬ 0    πŸ“Œ 0
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New Microscopy Technique Challenges Therapeutic Antibody Classification A super-resolution microscopy technique offers an unparalleled glimpse into how monoclonal antibodies bind to their targets on cancer cells to induce cell death.

Our work on lattice light-sheet TDI-DNA-PAINT and anti-CD20 immunotherapy antibodies is now featured in The Scientist magazine www.the-scientist.com. Many thanks to Sneha Khedkar for writing this fantastic piece. www.the-scientist.com/new-microsco...

25.03.2025 13:01 β€” πŸ‘ 4    πŸ” 0    πŸ’¬ 0    πŸ“Œ 0

πŸ”¬Happy to share our new preprint, where brightness is used to identify single molecule emission in 2D/3D, with a single camera ! Part of the PhD work of @laurent-le.bsky.social and Surabhi, great collaboration with @emmanuelfort.bsky.social from @instlangevin.bsky.social @ismolab.bsky.social #SMLM

04.03.2025 08:58 β€” πŸ‘ 62    πŸ” 22    πŸ’¬ 0    πŸ“Œ 0
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Anna-Karin Gustavsson on LinkedIn: Rice’s Gustavsson receives NSF CAREER Award to investigate dynamics of… Very honored and grateful to receive the NSF CAREER Award! Big thanks to the National Science Foundation (NSF) and to my fantastic research team and…

Congratulations to Rice Chemistry Prof. Anna-Karin Gustavsson for receiving the NSF CAREER.
@gustavssonlab.bsky.social #NSFCAREER #RiceChemistry

04.03.2025 18:31 β€” πŸ‘ 7    πŸ” 2    πŸ’¬ 0    πŸ“Œ 0
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Leaflet‐specific Structure and Dynamics of Solid and Polymer Supported Lipid Bilayers Polymer-supported or tethered lipid bilayers serve as versatile platforms for mimicking plasma membrane structure and dynamics, yet the impact of polymer supports on lipid bilayers remains largely un...

Happy to share our newest paper in Ang. Chem. and big thanks to @nkaredla.bsky.social, @faldalf.bsky.social and @tao-chen.bsky.social πŸ™ onlinelibrary.wiley.com/doi/10.1002/...

11.03.2025 07:58 β€” πŸ‘ 26    πŸ” 6    πŸ’¬ 2    πŸ“Œ 1
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πŸ§ͺParis Jussieu right now #standupforscience

07.03.2025 12:41 β€” πŸ‘ 54    πŸ” 6    πŸ’¬ 1    πŸ“Œ 2
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Science, research & public health face unprecedented attacks in the U.S.

We stand with our American colleagues & support the Stand Up for Science call.

Join the global march tomorrow, incl. in Paris! πŸ§ͺ✊

πŸ“ March 7, 13:30 – Place Jussieu
πŸ”— More info: standupforscience.fr

#StandUpForScience

06.03.2025 14:24 β€” πŸ‘ 264    πŸ” 82    πŸ’¬ 3    πŸ“Œ 5
Molecular Level Super-Resolution Fluorescence Imaging | Annual Reviews Over the last 30 years, fluorescence microscopy, renowned for its sensitivity and specificity, has undergone a revolution in resolving ever-smaller details. This advancement began with stimulated emis...

I'm thrilled to share that our review article, "Molecular Level Super-Resolution Fluorescence Imaging," has now been published online (www.annualreviews.org/content/jour...)! We provide a comprehensive overview of fluorescence super-res methods that push the limits towards molecular-scale imaging.

18.02.2025 15:52 β€” πŸ‘ 37    πŸ” 10    πŸ’¬ 0    πŸ“Œ 0