Author
Y.-L. Liu
Primary ORCID profile (0000-0002-8679-4133 · 1 paper)Unclaimed ORCID profile · follow to get notified of new preprints
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Biology Disciplines
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2017-2024 · peak 3/yrCo-Author Collaboration Network
10 top collaborators · 29 mutual co-author links11 papers
Recent·Most cited
An efficient peptide ligase engineered from a bamboo asparaginyl endopeptidase
X.-B. Wang, C.-H. Zhang, T. Zhang, H.-Z. Li, Y.-L. Liu, Z.-G. Xu, G. Lei, C.-J. Cai, Z.-Y. Guo
The paper engineers a bamboo-derived peptide ligase with improved activity by modifying its activation mechanism.
bioRxiv · Sep 7, 2023Biochemistry
The ghrelin receptor GHSR has two efficient agonists in an ancient fish species
H.-Z. Li, Y.-F. Wang, Y.-S. Zheng, Y.-L. Liu, Z.-G. Xu, Z.-Y. Guo
The study identifies that GHSR in coelacanth binds and is activated by motilin, while zebrafish and large yellow croaker GHSRs do not bind motilin, suggesting ancient fish GHSRs had two agonists.
bioRxiv · Jun 3, 2023 · PreprintBiochemistry
FAM237A, rather than peptide PEN and proCCK56-63, is a ligand of the orphan receptor GPR83
H.-Z. Li, Y.-F. Wang, X.-X. Shao, Y.-L. Liu, Z.-G. Xu, S.-L. Wang, Z.-Y. Guo
This study identifies FAM237A as the true ligand of GPR83, refuting previous claims that PEN and proCCK56-63 are agonists of this receptor.
bioRxiv · Sep 27, 2022 · PreprintBiochemistry
Development of esterase-resistant and highly active ghrelin analogs via thiol-ene click chemistry
H.-Z. Li, X.-X. Shao, L.-L. Shou, N. Li, Y.-L. Liu, Z.-G. Xu, Z.-Y. Guo
This study develops esterase-resistant and highly active ghrelin analogs using thiol-ene click chemistry, showing improved stability and activity in serum.
bioRxiv · Jun 29, 2022Biochemistry
Development of a novel bioluminescent activity assay for peptide ligases
C.-H. Zhang, X.-X. Shao, X.-B. Wang, L.-L. Shou, Y.-L. Liu, Z.-G. Xu, Z.-Y. Guo
The paper develops a bioluminescent assay to identify and characterize peptide ligases, finding that several plant species likely express these enzymes.
bioRxiv · Nov 1, 2021 · PreprintBiochemistry
Deep learning enables rapid and robust analysis of fluorescence lifetime imaging in photon-starved conditions
Y.-I. Chen, Y.-J. Chang, S.-C. Liao, T. D. Nguyen, J. Yang, Y.-A. Kuo, S. Hong, Y.-L. Liu, H. G. Rylander, S. R. Santacruz, T. E. Yankeelov, H.-C. Yeh
This paper introduces flimGANE, a deep learning method that rapidly and accurately generates FLIM images in low-photon conditions, outperforming traditional methods in speed and analysis accuracy.
bioRxiv · Dec 2, 2020 · PreprintCell Biology
Inhibition of Severe Acute Respiratory Syndrome Coronavirus 2 main protease by tafenoquine in vitro
Y. Chen, W.-H. Yang, L.-M. Huang, Y.-C. Wang, C.-S. Yang, Y.-L. Liu, M.-H. Hou, C.-L. Tsai, Y.-Z. Chou, B.-Y. Huang, C.-F. Hung, Y.-L. Hung, J.-S. Chen, Y.-P. Chiang, D.-Y. Cho, , M.-C. Hung
This study identifies tafenoquine as an inhibitor of SARS-CoV-2 main protease, showing it reduces protease activity and inhibits viral infection in vitro.
bioRxiv · Aug 14, 2020 · PreprintBiochemistry
In vivo multiphoton fluorescence imaging with polymer dots
A. M. Hassan, X. Wu, J. W. Jarrett, S. Xu, D. R. Miller, J. Yu, E. P. Perillo, Y.-L. Liu, D. T. Chiu, H.-C. Yeh, A. K. Dunn
This paper demonstrates the use of polymer dots for deep in vivo multiphoton imaging in mice, showing improved signal-to-background ratio and imaging depth.
bioRxiv · Nov 30, 2017Bioengineering