Asst. Prof. @ CU-Anschutz | gene regulation and protein folding | single-particle tracking | live-cell imaging | she/her

Joined November 2018
11 Photos and videos
Pinned Tweet
We have developed a cysteine-free, highly thermostable tagging system, UTag, that enables single-mRNA translation tracking in live cells. You may wonder how different tagging systems affect translation kinetics—we addressed this by performing a systematic comparison.
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We have developed a cysteine-free, highly thermostable tagging system, UTag, that enables single-mRNA translation tracking in live cells. You may wonder how different tagging systems affect translation kinetics—we addressed this by performing a systematic comparison.
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To further enhance its robust folding in intracellular environments, we engineered a cysteine-free variant with improved thermostable (Tm ~80 °C) that maintains the high UTag binding affinity. Excitingly, both intrabodies enable single-mRNA translation tracking in live cells.
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We benchmarked UTag against SunTag and ALFA-tag for single-mRNA translation tracking and observed comparable translation spot intensity and signal-to-noise ratios. Importantly, translation kinetics were also comparable across systems, as determined by both ACF and harringtonine.
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New preprint from our lab, led by Luis Aguilera! We have developed an open-source software, "MicroLive," to track single molecules in live cells. This one-step platform enables researchers without coding experience to perform single-molecule studies in a user-friendly interface!
MicroLive: An Image Processing Toolkit for Quantifying Live-cell Single-Molecule Microscopy biorxiv.org/content/10.1101/… #biorxiv_biophys
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Imaging single endogenous RNA in live cells comes true!
Single-molecule live-cell RNA imaging with CRISPR–Csm go.nature.com/3EJPKsM
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Ning Zhao retweeted
18 Feb 2025
Visualizing RNA in live cells using CRISPR @DoudnaLab @NatureBiotech nature.com/articles/s41587-0…
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Ning Zhao retweeted
IgGM: A Generative Model for Functional Antibody and Nanobody Design 1/ IgGM is a novel generative model designed to facilitate the de novo design of antibodies and nanobodies with functional specificity, focusing on their ability to bind specific antigens. This model uniquely generates both the sequences and structures of antibodies in a single step. 2/ The model consists of three main components: a pre-trained language model that extracts sequence features, a feature learning module to identify relevant features, and a prediction module to generate antibody sequences and predict the antibody-antigen complex structure. 3/ IgGM addresses a major challenge in antibody design by generating novel antibody sequences and their structures without the need for existing experimental antibody-antigen complex structures, making it suitable for scenarios involving new antigens. 4/ The model is capable of designing antibody CDR regions, which are crucial for antigen binding, and can also predict and design entire antibody structures, a significant advancement over existing methods that often require pre-existing structures or templates. 5/ IgGM excels in both antibody and nanobody design tasks, achieving superior performance in multiple design scenarios, such as generating antibodies with high specificity and binding affinity to antigens, outperforming previous methods in terms of sequence and structure fidelity. 6/ Its ability to design antibodies and nanobodies for specific epitopes, including the design of multiple CDR regions simultaneously, provides a versatile solution for therapeutic and diagnostic applications. 7/ Experimental results demonstrate IgGM's impressive accuracy, including higher success rates in docking performance and lower RMSD values compared to existing methods, showcasing its potential in the rapidly growing field of AI-driven drug design. 💻Code: github.com/TencentAI4S/IgGM 📜Paper: biorxiv.org/content/10.1101/… #AntibodyDesign #NanobodyDesign #GenerativeModels #MachineLearning #AIinHealthcare #DrugDiscovery #Bioinformatics #ComputationalBiology #DeepLearning #AIforMedicine #ProteinDesign
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Ning Zhao retweeted
15 Feb 2025
Emergency town hall at #BPS2025 Impact of U.S. policies on biophysics research and what you can do about it. Tuesday, February 18 1:30 pm - 3:30 pm Room 411
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Ning Zhao retweeted
12 Feb 2025
Making intrabodies from antibodies just got easier! Learn how we made 𝟭𝟵 intrabodies to bind and light up peptides and histone modifications in live cells. And thanks to Academia, all sequences are freely available. (video credit: Yuko Sato @YukoSatoT2) biorxiv.org/content/10.1101/…
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The first review paper from the Zhao lab is out today! This is a comprehensive review of not only tool development but also novel discoveries in translation. #CU_BMG #Biochem_Journal #NewPI Expanding the tagging toolbox for visualizing translation live portlandpress.com/biochemj/a…
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A big surprise from my lab! Happy Chinese New Year!
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We had a great time at MOLB retreat! Presented our work in ancient Greece themed costumes and sumitted Twin Cones in Winter Park. Thanks for organizing this fatastic retreat and hiking! @molbcu @prekerislab
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We're ready for the spooky season!
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Postdoc candidates, we'd love to "CU" here!
🧑‍🔬Are you thinking of doing a PostDoc? We would LOVE to “CU” here!🎉 Come to PEAKS, our Postdoc Recruitment event taking place April 7-8, 2025! 🧪 Present your Thesis work 🧑‍🏫 Meet our Faculty 🏫 Campus Tours 🤝 Networking Opportunities 💬  Engage with the CU Anschutz Community
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Beautiful work from the Stasevich lab! Imaging the full central dogma.@tim_stasevich
17 Feb 2024
A dream of our lab has been to image the full central dogma from a single endogenous gene, all live and with single molecule resolution. After many years we are happy to unveil a beautiful cell line that makes it possible. Check out our preprint (biorxiv.org/content/10.1101/…)! (1/n)
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Cannot agree more!
A truly amazing meeting from @BiophysicalSoc President TJ Ha @taekjip and the ultimate sacrifice from program chairs @IbrahimCisse_ and Elizabeth Villa @TheVillaLab!
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Ning Zhao retweeted
11 Sep 2023
Excited to share the work on single-molecule translation imaging of C9ORF72 repetitive RNA, spearheaded by @GosiaJl , Shaopeng Wang, and Daoyuan Dong, in collaboration with @shuying_sun, , @NingInScience , @tim_stasevich , now published on Nat Comm: nature.com/articles/s41467-0…
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CSU is hiring! Great science and colleagues!
22 Aug 2023
Our department is hiring! Come join us in Fort Collins, Colorado. Great environment for research and play. We encourage those studying biological processes using cell biology, imaging, and/or biophysical and structural approaches to apply. nature.com/naturecareers/job…
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