Polymer Coiled-Coil Conjugates: Potential for Development as a New Class of Therapeutic "Molecular Switch"

被引:36
作者
Deacon, Samuel P. E. [3 ]
Apostolovic, Bojana [1 ,2 ]
Carbajo, Rodrigo J. [4 ]
Schott, Anne-Kathrin [4 ]
Beck, Konrad [6 ]
Vicent, Maria J. [5 ]
Pineda-Lucena, Antonio [4 ]
Klok, Harm-Anton [1 ,2 ]
Duncan, Ruth [3 ]
机构
[1] Ecole Polytech Fed Lausanne, Inst Mat, CH-1015 Lausanne, Switzerland
[2] Ecole Polytech Fed Lausanne, Inst Sci & Ingn Chim, Lab Polymeres, CH-1015 Lausanne, Switzerland
[3] Welsh Sch Pharm, Ctr Polymer Therapeut, Cardiff CF10 3NB, S Glam, Wales
[4] CIPF, Struct Biol Lab, E-46012 Valencia, Spain
[5] CIPF, Med Chem Unit, Polymer Therapeut Lab, E-46012 Valencia, Spain
[6] Cardiff Univ, Sch Dent, Cardiff CF14 4XY, S Glam, Wales
基金
英国工程与自然科学研究理事会; 英国生物技术与生命科学研究理事会; 瑞士国家科学基金会;
关键词
HYBRID BLOCK-COPOLYMERS; IN-VITRO; PEPTIDES; AP-1; FOS; JUN; TRANSCRIPTION; DRUG; EXPRESSION; TARGETS;
D O I
10.1021/bm100843e
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
Polymer therapeutics, including polymeric drugs and polymer-protein conjugates, are clinically established as first-generation nanomedicines. Knowing that the coiled-coil peptide motif is fundamentally important in the regulation of many cellular and pathological processes, the aim of these studies was to examine the feasibility of designing polymer conjugates containing the coiled-coil motif as a putative therapeutic "molecular switch". To establish proof of concept, we prepared a mPEG-FosW(C) conjugate by reacting mPEG-maleimide (M-w 5522 g mol(-1) M-w/M-n 1.1) with a FosW peptide synthesized to contain a terminal cysteine residue (FosW(C)). Its ability to form a stable coil-coil heterodimer with the target c-Jun sequence of the oncogenic AP-1 transcription factor was investigated using 2D N-15-HSQC NMR together with a recombinantly prepared N-15-labeled c-Jun peptide ([N-15]r-c-Jun). Observation that heterodimerization was achieved and that the polymer did not sterically disadvantage hybridization suggests an important future for this new family of polymer therapeutics.
引用
收藏
页码:19 / 27
页数:9
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