Solid-phase supported polymer synthesis of sequence-defined, multifunctional poly(amidoamines)

被引:117
作者
Hartmann, L
Krause, E
Antonietti, M
Börner, HG
机构
[1] Max Planck Inst Colloids & Interfaces, MPI KGF Golm, D-14424 Potsdam, Germany
[2] Inst Mol Pharmacol, D-13125 Berlin, Germany
关键词
D O I
10.1021/bm050884k
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A novel synthesis route toward multifunctional, sequence-defined polyamides is described. A fully automated, solid-phase supported polymer synthesis was developed and utilized to obtain linear poly(amidoamine) segments (PAAs) that exhibit the absence of molecular weight and chemical distribution. This was achieved by an alternating assembly of diacids and diamines, using a forced step-growth mechanism, and driving each coupling step to completion. Within the monodisperse PAA segment, functionalities can be precisely positioned along the polymer chain allowing local control of the chain properties. The versatility of the approach was demonstrated by the conjugation of the monodisperse PAA segment toward an oligopeptide, leading to a single component block copolymer as verified by mass spectrometry. Moreover, two different poly(ethylene oxide)-PAA conjugates were synthesized utilizing the direct, solid-phase supported route. By varying the PAA repeat unit, the cationic nature of the PAA segment was adjusted, demonstrating the potential of the approach. The products were characterized by means of H-1 NMR and matrix-assisted laser desorption mass spectrometry (MALDI-TOF-MS) methods, which confirmed the chemical structures conclusively.
引用
收藏
页码:1239 / 1244
页数:6
相关论文
共 34 条
[1]   Malachite green, a valuable reagent to monitor the presence of free COOH on the solid-phase [J].
Attardi, ME ;
Porcu, G ;
Taddei, M .
TETRAHEDRON LETTERS, 2000, 41 (38) :7391-7394
[2]   Synthesis of alkaloid natural products using solid-supported reagents and scavengers [J].
Baxendale, IR ;
Ley, SV .
CURRENT ORGANIC CHEMISTRY, 2005, 9 (15) :1521-1534
[3]  
Chan W., 1999, Fmoc solid phase peptide synthesis: a practical approach
[4]   PYBOP - A NEW PEPTIDE COUPLING REAGENT DEVOID OF TOXIC BY-PRODUCT [J].
COSTE, J ;
LENGUYEN, D ;
CASTRO, B .
TETRAHEDRON LETTERS, 1990, 31 (02) :205-208
[5]  
De Gennes PG., 1979, SCALING CONCEPTS POL
[6]   The dawning era of polymer therapeutics [J].
Duncan, R .
NATURE REVIEWS DRUG DISCOVERY, 2003, 2 (05) :347-360
[7]   Rational design of oligopeptide organizers for the formation of poly(ethylene oxide) nanofibers [J].
Eckhardt, D ;
Groenewolt, M ;
Krause, E ;
Börner, HG .
CHEMICAL COMMUNICATIONS, 2005, (22) :2814-2816
[8]   Amphoteric linear poly(amido-amine)s as endosomolytic polymers: Correlation between physicochemical and biological properties [J].
Ferruti, P ;
Manzoni, S ;
Richardson, SCW ;
Duncan, R ;
Pattrick, NG ;
Mendichi, R ;
Casolaro, M .
MACROMOLECULES, 2000, 33 (21) :7793-7800
[9]  
Ferruti P, 2002, MACROMOL RAPID COMM, V23, P332, DOI 10.1002/1521-3927(20020401)23:5/6<332::AID-MARC332>3.0.CO
[10]  
2-I