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Tuning autophagy-inducing activity a...
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Zhang, Yunjiao.
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Tuning autophagy-inducing activity and toxicity for lanthanide nanocrystals
紀錄類型:
書目-電子資源 : Monograph/item
正題名/作者:
Tuning autophagy-inducing activity and toxicity for lanthanide nanocrystals/ by Yunjiao Zhang.
作者:
Zhang, Yunjiao.
出版者:
Singapore :Springer Singapore : : 2022.,
面頁冊數:
xv, 156 p. :ill. (chiefly col.), digital ;24 cm.
附註:
"Doctoral thesis accepted by University of Science and Technology of China, Hefei, China."
內容註:
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.
Contained By:
Springer Nature eBook
標題:
Nanocrystals. -
電子資源:
https://doi.org/10.1007/978-981-16-8166-0
ISBN:
9789811681660
Tuning autophagy-inducing activity and toxicity for lanthanide nanocrystals
Zhang, Yunjiao.
Tuning autophagy-inducing activity and toxicity for lanthanide nanocrystals
[electronic resource] /by Yunjiao Zhang. - Singapore :Springer Singapore :2022. - xv, 156 p. :ill. (chiefly col.), digital ;24 cm. - Springer theses,2190-5061. - Springer theses..
"Doctoral thesis accepted by University of Science and Technology of China, Hefei, China."
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.
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.
ISBN: 9789811681660
Standard No.: 10.1007/978-981-16-8166-0doiSubjects--Topical Terms:
605740
Nanocrystals.
LC Class. No.: TA418.9.N35 / Z53 2022
Dewey Class. No.: 620.115
Tuning autophagy-inducing activity and toxicity for lanthanide nanocrystals
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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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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.
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