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Cell-Penetrating Peptides

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Cover of 'Cell-Penetrating Peptides'

Table of Contents

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    Book Overview
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    Chapter 1 Classes of Cell-Penetrating Peptides.
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    Chapter 2 Cell-Penetrating Peptides
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    Chapter 3 Prediction of Cell-Penetrating Peptides
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    Chapter 4 Computer-Aided Virtual Screening and Designing of Cell-Penetrating Peptides.
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    Chapter 5 Investigating Membrane Interactions and Structures of CPPs.
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    Chapter 6 Determining the Effects of Membrane-Interacting Peptides on Membrane Integrity.
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    Chapter 7 Study of CPP Mechanisms by Mass Spectrometry.
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    Chapter 8 Methods to Study the Role of the Glycocalyx in the Uptake of Cell-Penetrating Peptides
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    Chapter 9 Toxicity, Immunogenicity, Uptake, and Kinetics Methods for CPPs
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    Chapter 10 Unraveling the Mechanisms of Peptide-Mediated Delivery of Nucleic Acids Using Electron Microscopy.
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    Chapter 11 SCARA Involvement in the Uptake of Nanoparticles Formed by Cell-Penetrating Peptides
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    Chapter 12 Protein Mimicry and the Design of Bioactive Cell-Penetrating Peptides.
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    Chapter 13 Pepducins and Other Lipidated Peptides as Mechanistic Probes and Therapeutics.
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    Chapter 14 Identification and Characterization of Homing Peptides Using In Vivo Peptide Phage Display.
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    Chapter 15 The Antimicrobial and Antiviral Applications of Cell-Penetrating Peptides
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    Chapter 16 Visualizing Actin Architectures in Cells Incubated with Cell-Penetrating Peptides.
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    Chapter 17 Cell-Penetrating Peptides as Carriers for Transepithelial Drug Delivery In Vitro.
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    Chapter 18 A Pathway Toward Tumor Cell-Selective CPPs?
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    Chapter 19 PepFects and NickFects for the Intracellular Delivery of Nucleic Acids
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    Chapter 20 In Vitro Assays to Assess Exon Skipping in Duchenne Muscular Dystrophy.
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    Chapter 21 Applications of ApoB LDLR-Binding Domain Approach for the Development of CNS-Penetrating Peptides for Alzheimer's Disease.
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    Chapter 22 CPP-Based Delivery System for In Vivo Gene Delivery
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    Chapter 23 Application of CPPs for Brain Delivery
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    Chapter 24 Intracellular Delivery of Nanoparticles with Cell Penetrating Peptides.
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    Chapter 25 Cell-Penetrating Peptides
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    Chapter 26 Cell Penetrating Peptides for Chemical Biological Studies.
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    Chapter 27 Experiences with CPP-Based Self Assembling Peptide Systems for Topical Delivery of Botulinum Toxin.
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    Chapter 28 Applications of CPPs in Genome Modulation of Plants.
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    Chapter 29 DNA Transfer into Animal Cells Using Stearylated CPP Based Transfection Reagent.
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    Chapter 30 Live Cell Genomics: Cell-Specific Transcriptome Capture in Live Tissues and Cells.
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    Chapter 31 Live Cell Genomics: RNA Exon-Specific RNA-Binding Protein Isolation.
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    Chapter 32 ERRATUM TO: Methods to Study the Role of the Glycocalyx in the Uptake of Cell-Penetrating Peptides.
Attention for Chapter 31: Live Cell Genomics: RNA Exon-Specific RNA-Binding Protein Isolation.
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Chapter title
Live Cell Genomics: RNA Exon-Specific RNA-Binding Protein Isolation.
Chapter number 31
Book title
Cell-Penetrating Peptides
Published in
Methods in molecular biology, January 2015
DOI 10.1007/978-1-4939-2806-4_31
Pubmed ID
Book ISBNs
978-1-4939-2805-7, 978-1-4939-2806-4
Authors

Thomas J. Bell, James Eberwine

Editors

Ülo Langel

Abstract

RNA-binding proteins (RBPs) are essential regulatory proteins that control all modes of RNA processing and regulation. New experimental approaches to isolate these indispensable proteins under in vivo conditions are needed to advance the field of RBP biology. Historically, in vitro biochemical approaches to isolate RBP complexes have been useful and productive, but biological relevance of the identified RBP complexes can be imprecise or erroneous. Here we review an inventive experimental to isolate RBPs under the in vivo conditions. The method is called peptide nucleic acid (PNA)-assisted identification of RBP (PAIR) technology and it uses cell-penetrating peptides (CPPs) to deliver photo-activatible RBP-capture molecule to the cytoplasm of the live cells. The PAIR methodology provides two significant advantages over the most commonly used approaches: (1) it overcomes the in vitro limitation of standard biochemical approaches and (2) the PAIR RBP-capture molecule is highly selective and adaptable which allows investigators to isolate exon-specific RBP complexes. Most importantly, the in vivo capture conditions and selectivity of the RBP-capture molecule yield biologically accurate and relevant RBP data.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 15 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 15 100%

Demographic breakdown

Readers by professional status Count As %
Researcher 6 40%
Student > Ph. D. Student 3 20%
Professor > Associate Professor 2 13%
Lecturer 1 7%
Student > Master 1 7%
Other 1 7%
Unknown 1 7%
Readers by discipline Count As %
Agricultural and Biological Sciences 5 33%
Biochemistry, Genetics and Molecular Biology 3 20%
Chemistry 2 13%
Medicine and Dentistry 1 7%
Computer Science 1 7%
Other 2 13%
Unknown 1 7%