Drew Carson

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Drew Carson

Drew Carson

@DrewCarson712

PhD Candidate in Link Lab at Princeton; Motivated by bacterial natural products and their biosynthesis and bioactivities.

Katılım Ekim 2021
252 Takip Edilen108 Takipçiler
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A. James Link
A. James Link@ajlinklab·
The latest Link lab paper is out @BiochemistryACS!: doi.org/10.1021/acs.bi… This work, led by Angela Zhu, focuses on the cysimiditides, a new subfamily of #RiPPs. The cysimiditides include a tetracysteine motif that coordinates a zinc ion and a single aspartimide moiety.
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Michael Fischbach
Michael Fischbach@mfgrp·
Today we report that an engineered skin bacterium, swabbed gently on the head of a mouse, can unleash a potent antibody response against a pathogen. Could lead to topical vaccines that are applied in a cream. @DjenetBousbaine led the charge... @Nature 1/55
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Drew Carson
Drew Carson@DrewCarson712·
Excited to be at @BostonBacteria at Boston Univ! Looking forward to some great science #BBM2024 🧫 I’m presenting poster number 104 tomorrow, come say hi!
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Howard Salis
Howard Salis@hsalis·
Psst. Hey. Yeah you. Want to build 100s to 1000s of plasmids (*any sequence* up to ~6000 bp) for about $10 to $40 each? salislab.net/software/build… Try it out ... feedback is welcomed & encouraged :)
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Datta Lab
Datta Lab@TheSquishyLab·
Excited to release our latest work, led by Sebastian Gonzalez La Corte (@sesgonzalez) with Ned Wingreen: doi.org/10.1101/2024.0…! Here, we show that polymers unexpectedly sculpt proliferating bacterial colonies into spaghetti-like "cables".🦠🍝 Tweetorial follows! [1/10]
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Drew Carson
Drew Carson@DrewCarson712·
Our new paper is just out now in ACS Chemical Biology! Here we uncover the transport pathway that the antimicrobial lasso peptide cloacaenodin uses to be able to kill susceptible bacteria. This helps explain the narrow-spectrum activity we observe. pubs.acs.org/doi/10.1021/ac…
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Drew Carson
Drew Carson@DrewCarson712·
Our lab's work highly suggests that narrow-spectrum antimicrobial lasso peptides (MccJ25, cloacaenodin, ubonodin) evolved their specificities as a result of their hijacking unique, outer membrane proteins (using active transport) to cross the formidable Gram-neg outer membrane.
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