The Fluorescent Protein Database. tweets by @TalleyJLambert

Joined January 2019
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Hi Fluorescence friends! Please follow future updates on Bluesky: bsky.app/profile/fpbase.org
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They all retain the alias mStayGold, and so will all still show up when one searches for "mStayGold"
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This exercise was less informative than I'd hoped, but perhaps it's interesting to someone else: spectroscopically-inferred estimates of densities of states for a selection of fluorescent proteins spanning the visible spectrum. Data from @FPbase.
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recently hit 2,000,000 sessions on @FPbase ! 📈
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Mutagenesis of #FbFP #LOV domain: 🟠 22 variants with 486-512 nm emission maxima 🟠 three-channel imaging via spectral unmixing 🟠 two-channel fluorescence lifetime unmixing doi.org/10.1101/2022.12.09.5… Congratulations, @ivangushchin, @Aynya5, and all the authors! @FPbase
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Replying to @FPbase @bakermind
took a look, there are 90 2P spectra currently available in the database. So, this is a user interface problem rather than a data storage problem 😬 ... (GM units are also stored in the database, but easily accessible) my apologies!
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Replying to @FPbase @bakermind
If the data has been published but is missing from the corresponding fpbase page, you can add it at fpbase.org/submit/ (User submissions are how FPbase gets populated)
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Replying to @bakermind
No not each molecule, but Misha Drobizhev contributed the majority of the 2P cross sections he’a collected (🙏!). So if the 2P data is published, it should be available on the respective FP page.
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Replying to @bakermind
Yeah it’s a common request (so little time). There’s lots of 2P data in fpbase, do you just want like a dedicated page to make it easier to find for example?
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Chapter on using FPbase tools out now in the MMB issue on FPs. Thank you for editing @mayankdu!
Happy to share the Methods in Molecular Biology issue on Fluorescent Proteins 🌈🎉😀. Including many “much awaited” protocols on and about Fluorescent Proteins/applications. A big THANKS to authors across the globe for contributing. 👏🏻💐 link.springer.com/book/10.10…
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Yes, but with more dyes, proteins, and filters, and no commercial interest 😉
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Replying to @mycroscopy
Wow, that’s a really impressive amount of organization! Very cool, congrats
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this is genius: @helsinkiuni BioImaging Unit utilizes @FPbase to allow users test their fluorophores fpbase.org/microscope/u4gqNc… cc @Daniel_Wa19
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anyone out there routinely express FPs in Chlamydomonas? any modern suggestions for SNR? (presumably red, but any expression gotchas?)
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Replying to @beniroquai
That would be 50% of max Extinction coefficient (not QE). If you’re asking whether it “works”, it will be case-specific. Will require more illum power, so more damaging to sample. And may generate more background, depending on sample. But with enough power you’ll get photons :)
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🥁 Delighted to announce that our FPCountR paper is now on bioRxiv! In this paper we describe the development of a method to allow absolute fluorescent protein quantification using microplate readers for synthetic circuit characterisation. biorxiv.org/content/10.1101/… 🧵
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