The Ho Lab @ColumbiaMed @Columbia_MI - using cryoEM to explore how membrane protein complexes mediate host-pathogen interactions in malaria parasites!

New York, NY
Joined August 2019
Join speaker Chi-Min Ho @Columbia at #CS3Dbiologicalfunction2026. Chi-Min’s research integrates structural biology approaches to investigate host-pathogen interactions in malaria parasites. Extended abstract deadline: July 27, 2026 hubs.li/Q04p7b7x0
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The Ho Lab retweeted
Incredibly proud of Messi Haile @mehsehret, a @cmholab founding member, for her beautiful work uncovering the inner workings of a central piece of the malaria parasite invasion machinery: the malarial moving junction, out today in @CellPressNews ! tinyurl.com/4p3md2eb 🦠❄️🔬
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The Ho Lab retweeted
So incredibly excited and grateful to be joining the Burroughs Wellcome Fund PATH family! Thank you @BWFUND and the selection committee members for supporting and believing in our vision, and congrats to the other 2026 PATH Investigators!!! 🥳
BWF Announces the 2026 Investigators in the Pathogenesis of Infectious Disease bwfund.org/news/bwf-announce… #bwfpath
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Happy to share our new review of kainate receptor structure and gating. @shantigangwar @MariaKarela3 @LauraYen42 frontiersin.org/journals/pha…
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The Ho Lab retweeted
Learn how our hunt for the native structure of top #antimalarial target PfATP4🧂led to the discovery of PfABP, an unknown essential binding partner, out now! @natcomms 👉 rdcu.be/eLRlH 🦠🔬❄️ A team effort by @mehsehret @cmholab & Anurag Shukla @AkhilVaidya1 #cryoEM
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New online! Dynamic TOM–TIM23 supercomplex directs mitochondrial protein translocation and sorting bit.ly/4n7AJC4
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Structures of kainate receptor channel GluK2 in the apo closed and open conducting states, both with 2-fold symmetrical LBD layer. To open the channel, we used agonist kainate and positive allosteric modulator BPAM but no Concanavalin A! @shantigangwar nature.com/articles/s41594-0…
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The Ho Lab retweeted
Our #CryoET story on how a top antimalarial drug candidate perturbs the native malarial translation machinery is out @NatureSMB🥳rdcu.be/eBbrH Massive team effort led by @leonie_anton @mehsehret @Wenjing_Cheng_ in collaboration with @DziekanJerzy @CowmanAlan #teamtomo
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The Ho Lab retweeted
Thank you so much @hypothesisfund and @Yeh_Lab for supporting us in this new venture!! We're excited to get started! 🦠🔬❄️
Replying to @Hypothesisfund
3/ Awardee @mimi1inh tackles the complex challenges of protein sequencing by leveraging molecular machinery made by microbes. Her work could revolutionize how we study protein function + structure, & our understanding of biology🤯. 🥳Congrats Dr. Ho! @Columbia 🙏#HFScout @Yeh_Lab
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3/ Awardee @mimi1inh tackles the complex challenges of protein sequencing by leveraging molecular machinery made by microbes. Her work could revolutionize how we study protein function + structure, & our understanding of biology🤯. 🥳Congrats Dr. Ho! @Columbia 🙏#HFScout @Yeh_Lab
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🌠 We're thrilled to announce our latest @HypothesisFund awardees and their groundbreaking projects! From optimizing enzymes, to protein sequencing, and membrane 'functional hotspots', each of these projects holds the potential to be broadly transformative for science! 1/ 🧵
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Vertebrate retrotransposons are the future of gene therapy. But how do they insert their genes? 🔥🔥 Thrilled to present part 2 of my postdoctoral work with @NogalesLab @CollinsRNPLab @berkeleyMCB where we investigate this using #CryoEM and transgene insertion in 🧪 and cells!
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The Ho Lab retweeted
The human mitochondrial ClpXP is uniquely assembled and regulated compared to its bacterial counterparts. Congrats to Kelly Chen on her years of hard work on this challenging complex! biorxiv.org/content/10.1101/…
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The Ho Lab retweeted
We have a fully-funded postdoc position in the @cmholab in #NYC to study how #membraneproteins drive host-pathogen interactions in #malaria parasites using #CryoEM and #CryoET!🦠❄️🔬Email [email protected] with your CV to apply! tinyurl.com/5n96rkfm #teamtomo
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