Biological-synthetic hybrid block copolymers: Combining the best from two worlds

被引:212
作者
Klok, HA [1 ]
机构
[1] Ecole Polytech Fed Lausanne, Inst Mat, Lab Polymeres, CH-1015 Lausanne, Switzerland
关键词
block copolymers; peptides; proteins; synthesis;
D O I
10.1002/pola.20527
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Although biopolymers and synthetic polymers share many common features, each of these two classes of materials is also characterized by a distinct and very specific set of advantages and disadvantages. Combining biopolymer elements with synthetic polymers into a single macromolecular conjugate is an interesting strategy for synergetically merging the properties of the individual components and overcoming some of their limitations. This article focuses on a special class of biological-synthetic hybrids that are obtained by site-selective conjugation of a protein or peptide and a synthetic polymer. The first part of the article gives an overview of the different liquid-phase and solid-phase techniques that have been developed for the synthesis of well-defined, that is, site-selectively conjugated, synthetic polymer-protein hybrids. In the second part, the properties and potential applications of these materials are discussed. The conjugation of biological and synthetic macromolecules allows the modulation of protein binding and recognition properties and is a powerful strategy for mediating the self-assembly of synthetic polymers. Synthetic polymer-protein hybrids are already used as medicines and show significant promise for bio-analytical applications and bioseparations. (C) 2004 Wiley Periodicals, Inc.
引用
收藏
页码:1 / 17
页数:17
相关论文
共 71 条
  • [11] Therapeutic antibody fragments with prolonged in vivo half-lives
    Chapman, AP
    Antoniw, P
    Spitali, M
    West, S
    Stephens, S
    King, DJ
    [J]. NATURE BIOTECHNOLOGY, 1999, 17 (08) : 780 - 783
  • [12] SITE-SPECIFIC CONJUGATION OF A TEMPERATURE-SENSITIVE POLYMER TO A GENETICALLY-ENGINEERED PROTEIN
    CHILKOTI, A
    CHEN, GH
    STAYTON, PS
    HOFFMAN, AS
    [J]. BIOCONJUGATE CHEMISTRY, 1994, 5 (06) : 504 - 507
  • [13] Self-assembling polymer-peptide conjugates: Nanostructural tailoring
    Collier, JH
    Messersmith, PB
    [J]. ADVANCED MATERIALS, 2004, 16 (11) : 907 - 910
  • [14] Commentary - The origin of pegnology
    Davis, FF
    [J]. ADVANCED DRUG DELIVERY REVIEWS, 2002, 54 (04) : 457 - 458
  • [15] Size-dependent control of the binding of biotinylated proteins to streptavidin using a polymer shield
    Ding, ZL
    Fong, RB
    Long, CJ
    Stayton, PS
    Hoffman, AS
    [J]. NATURE, 2001, 411 (6833) : 59 - 62
  • [16] The dawning era of polymer therapeutics
    Duncan, R
    [J]. NATURE REVIEWS DRUG DISCOVERY, 2003, 2 (05) : 347 - 360
  • [17] Comb-like and block liquid crystalline polymers for biological applications
    Gallot, B
    [J]. PROGRESS IN POLYMER SCIENCE, 1996, 21 (06) : 1035 - 1088
  • [18] Pegaspargase: a review of clinical studies
    Graham, ML
    [J]. ADVANCED DRUG DELIVERY REVIEWS, 2003, 55 (10) : 1293 - 1302
  • [19] Hamachi I, 1999, EUR J ORG CHEM, V1999, P539
  • [20] Effect of pegylation on pharmaceuticals
    Harris, JM
    Chess, RB
    [J]. NATURE REVIEWS DRUG DISCOVERY, 2003, 2 (03) : 214 - 221