Tuning autophagy-inducing activity and toxicity for lanthanide nanocrystals / Yunjiao Zhang.

This thesis presents a simple, yet highly effective surface engineering solution that uses non-covalent binding peptides to control the autophagy-inducing activity of nanomaterials and nanodevices. The author presents RE-1, a short synthetic peptide that sequence-specifically binds to lanthanide (LN...

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Bibliographic Details
Main Author: Zhang, Yunjiao (Author)
Format: eBook
Language:English
Published: Singapore : Springer, [2022]
Series:Springer theses.
Subjects:
Online Access:Click for online access

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520 |a This thesis presents a simple, yet highly effective surface engineering solution that uses non-covalent binding peptides to control the autophagy-inducing activity of nanomaterials and nanodevices. The author presents RE-1, a short synthetic peptide that sequence-specifically binds to lanthanide (LN) oxide and upconversion nanocrystals with high affinity, which was discovered using an innovative phage display approach. RE-1 effectively inhibits the autophagy-inducing activity and toxicity of these nanocrystals by forming a stable coating layer on the surface of the nanoparticles, and by reducing their sedimentation and cell interaction. RE- 1 and its variants provide a versatile tool for tuning cell interactions in order to achieve the desired level of autophagic response and are useful for the various diagnostic and therapeutic applications of LN-based nanomaterials and nanodevices. 
505 0 |a Introduction -- Phage display identifies a specific high-affinity binding peptide RE-1 for lanthanide (LN) nanomaterials -- RE-1 forms a stable coating layer on the surface of upconversion nanoparticles / nanocrystals (UCN) -- Reduction of UCN sedimentation and nanomaterial-cell interaction by RE-1 coating -- RE-1 coating abrogates autophagy induction and toxicity for UCN in vitro and in vivo -- Enhancement of cell interaction and autophagy induction by coating with RE-1-RGD.-Conclusion and prospect. 
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