Effects of Charge and Charge Distribution on the Cellular Uptake of Multivalent Arginine‐Containing Peptide–Polymer Conjugates. Issue 15 (24th September 2013)
- Record Type:
- Journal Article
- Title:
- Effects of Charge and Charge Distribution on the Cellular Uptake of Multivalent Arginine‐Containing Peptide–Polymer Conjugates. Issue 15 (24th September 2013)
- Main Title:
- Effects of Charge and Charge Distribution on the Cellular Uptake of Multivalent Arginine‐Containing Peptide–Polymer Conjugates
- Authors:
- Koschek, Katharina
Dathe, Margitta
Rademann, Jörg - Abstract:
- <abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <p>Copolymers of <italic>N</italic>‐(2‐hydroxypropyl)methacrylamide (HPMA) and <italic>N</italic>‐methacryloyl‐β‐alaninyl‐<italic>S</italic>‐benzyl thioester were prepared by employing free radical or RAFT conditions and denominated as "NCL polymers". The copolymer with a polydispersity index of 1.2–1.3 was used for the direct conjugation of unprotected peptides and peptide mixtures bearing differentially loaded side chains by native chemical ligation reactions conducted in aqueous buffer. Uptake into human HeLa cells was correlated with the overall surface charge and the <italic>ζ</italic> potentials of the peptide–polymer conjugates. Most notable were the differential effects found for various multivalent peptide–polymer conjugates containing arginine residues. Although positive <italic>ζ</italic> potentials were required for cellular uptake of the peptide–polymer conjugates, this sole charge effect was strongly dominated by the effect exerted by the relative distribution of arginine residues. Polymers conjugated with nona‐arginine peptides were over‐proportionally taken up, relative to their surface charge, compared to polymers with random distribution of single arginine residues. In view of these findings, peptide–polymer compositions suitable for efficient cellular uptake with negligible toxicity at polymer concentrations relevant for intracellular functional studies were determined.</p> </abstract>
- Is Part Of:
- Chembiochem. Volume 14:Issue 15(2013)
- Journal:
- Chembiochem
- Issue:
- Volume 14:Issue 15(2013)
- Issue Display:
- Volume 14, Issue 15 (2013)
- Year:
- 2013
- Volume:
- 14
- Issue:
- 15
- Issue Sort Value:
- 2013-0014-0015-0000
- Page Start:
- 1982
- Page End:
- 1990
- Publication Date:
- 2013-09-24
- Subjects:
- Biochemistry -- Periodicals
Molecular biology -- Periodicals
Pharmaceutical chemistry -- Periodicals
572 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1439-7633 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/cbic.201300365 ↗
- Languages:
- English
- ISSNs:
- 1439-4227
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3133.490980
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 3230.xml