2018
DOI: 10.1016/j.progpolymsci.2017.12.001
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Protein-mimetic peptide nanofibers: Motif design, self-assembly synthesis, and sequence-specific biomedical applications

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Cited by 159 publications
(107 citation statements)
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“…Various self-assembling peptide nanofibers have been employed as advanced materials in different biomedical applications. [16] For example, peptide and protein amyloids have been widely used for medical imaging, tissue engineering, and drug delivery. [17] Hybrids based peptide nanofibers have been utilized for targeting and imaging tumor cells.…”
Section: Introductionmentioning
confidence: 99%
“…Various self-assembling peptide nanofibers have been employed as advanced materials in different biomedical applications. [16] For example, peptide and protein amyloids have been widely used for medical imaging, tissue engineering, and drug delivery. [17] Hybrids based peptide nanofibers have been utilized for targeting and imaging tumor cells.…”
Section: Introductionmentioning
confidence: 99%
“…Therefore, the use of biomolecules in NP syntheses has received attention as a potential 'green synthesis' vehicles for the morphological and functional regulation of inorganic nanomaterials. [3][4][5] Amongst the plethora of available biological molecules, peptides have attracted particular attention as valuable tools in bionanotechnology, [6][7][8][9][10][11][12] because of their diverse functionalities and, with certain peptides, the potential for specic binding to particular materials (both organic and inorganic). [13][14][15] Various peptides have been utilised in the functionalisation of nanomaterials, 13,16,17 the control of NP synthesis, 18,19 as biotemplating for morphological control, 20 and biocatalysts for the NP crystalisation.…”
mentioning
confidence: 99%
“…These results demonstrated that the endocytic uptake mechanisms involved in CaP nanoparticles were through the clathrin-mediated and caveolae-mediated cellular uptake pathway, but mainly in the clathrin-mediated pathway which subsequently delivered cargo into the endosome and then transferred into the lysosome, which led to DNA degradation and low transfection efficiency [13,18,19]. Thus, it was very crucial to alter the cellular uptake pathway and subsequently change the intracellular profiles for improving the efficacy of gene vectors.…”
Section: Endocytic Mechanisms Involved In Cap-ma Non-viral Vectorsmentioning
confidence: 96%
“…To date, numerous researchers focused on the design and construction of gene delivery vectors and made attempts to address the challenges. As for the non-viral delivery vectors, they often suffer insufficient performance due to poor transfection efficiency, relatively high toxicity, inadequate cellular uptake and gene degradation in endosome or lysosome, which significantly hampers the application in the clinic [1,[12][13][14]. Viral delivery vectors possess innate machinery to overcome cellular barriers, however, non-viral delivery vectors require great effort to rationally design to overcome these barriers.…”
Section: Introductionmentioning
confidence: 99%