B
Bing Xu
Researcher at Brandeis University
Publications - 373
Citations - 29970
Bing Xu is an academic researcher from Brandeis University. The author has contributed to research in topics: Self-healing hydrogels & Cancer cell. The author has an hindex of 83, co-authored 357 publications receiving 26713 citations. Previous affiliations of Bing Xu include University of Pennsylvania & University of Hong Kong.
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Using enzymatic reactions to enhance the photodynamic therapy effect of porphyrin dityrosine phosphates
TL;DR: The synthesis and photodynamic therapy (PDT) effect of a porphyrin derivative containing tyrosine phosphate is reported, which promises a new, useful approach to develop PDT agents.
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L-Rhamnose-containing supramolecular nanofibrils as potential immunosuppressive materials
Fan Zhao,Balthasar A. Heesters,Balthasar A. Heesters,Isaac M. Chiu,Yuan Gao,Junfeng Shi,Ning Zhou,Michael C. Carroll,Bing Xu +8 more
TL;DR: An l-rhamnose-based hydrogelator self-assembles to form nanofibrils, which suppress the antibody response of mice to phycoerythrin (PE), a fluorescent protein antigen.
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Enzyme-Instructed Self-Assembly of Peptides Containing Phosphoserine to Form Supramolecular Hydrogels as Potential Soft Biomaterials.
TL;DR: Exchanging the positions of phosphorylated serine and tyrosine in the peptide backbone provides insights on how the specific molecular structures influence self-assembling behaviors of small peptides and the subsequent cellular responses.
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Magnetic nanoparticles for direct protein sorting inside live cells
TL;DR: This work reports the first example of the biofunctional magnetic nanoparticles as a “magnetic dock” for directly sorting proteins inside live cells and may ultimately contribute to the exploration of the functions of proteins via the selective, spatiotemporal control of the proteins by a magnetic force.
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Trypsin-Instructed Self-Assembly on Endoplasmic Reticulum for Selectively Inhibiting Cancer Cells: Dedicated to Professor George M. Whitesides on the occasion of his 80th birthday.
TL;DR: An easily accessible branched peptide that consists of a D‐tetrapeptide backbone and a branch with the sequence of KYDKKKKDG, being an EISA substrate of typsin‐1 (PRSS1), selectively inhibits cancer cells is reported.