Recent Progress Toward the Templated Synthesis and Directed Evolution of Sequence-Defined Synthetic Polymers

被引:81
作者
Brudno, Yevgeny [1 ,2 ]
Liu, David R. [1 ,2 ]
机构
[1] Harvard Univ, Dept Chem & Chem Biol, Cambridge, MA 02138 USA
[2] Harvard Univ, Howard Hughes Med Inst, Cambridge, MA 02138 USA
来源
CHEMISTRY & BIOLOGY | 2009年 / 16卷 / 03期
基金
美国国家卫生研究院;
关键词
SITE-SPECIFIC INCORPORATION; PEPTIDE NUCLEIC-ACIDS; HIV-1; REVERSE-TRANSCRIPTASE; UNNATURAL AMINO-ACIDS; DNA-POLYMERASE; GENETIC-CODE; COMBINATORIAL SELECTION; 1,5-ANHYDROHEXITOL NUCLEOTIDES; ENZYMATIC-SYNTHESIS; DRUG-DELIVERY;
D O I
10.1016/j.chembiol.2009.02.004
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
Biological polymers such as nucleic acids and proteins are ubiquitous in living systems, but their ability to address problems beyond those found in nature is constrained by factors such as chemical or biological instability, limited building-block functionality, bioavailability, and immunogenicity. In principle, sequence-defined synthetic polymers based on nonbiological monomers and backbones might overcome these constraints; however, identifying the sequence of a synthetic polymer that possesses a specific desired functional property remains a major challenge. Molecular evolution can rapidly generate functional polymers but requires a means of translating amplifiable templates such as nucleic acids into the polymer being evolved. This review covers recent advances in the enzymatic and nonenzymatic templated polymerization of nonnatural polymers and their potential applications in the directed evolution of sequence-defined synthetic polymers.
引用
收藏
页码:265 / 276
页数:12
相关论文
共 162 条
[1]  
Allart B, 1999, CHEM-EUR J, V5, P2424, DOI 10.1002/(SICI)1521-3765(19990802)5:8<2424::AID-CHEM2424>3.0.CO
[2]  
2-W
[3]   Intelligent Drug Delivery Systems: Polymeric Micelles and Hydrogels [J].
Alvarez-Lorenzo, Carmen ;
Concheiro, Angel .
MINI-REVIEWS IN MEDICINAL CHEMISTRY, 2008, 8 (11) :1065-1074
[4]  
AMON R, 1989, HORIZ BIOCH BIOPHYS, V9, P33
[5]   RNA: Prebiotic product, or biotic invention? [J].
Anastasi, Carole ;
Buchet, Fabien F. ;
Crowe, Michael A. ;
Parkes, Alastair L. ;
Powner, Matthew W. ;
Smith, James M. ;
Sutherland, John D. .
CHEMISTRY & BIODIVERSITY, 2007, 4 (04) :721-739
[6]   Foreign body reaction to biomaterials [J].
Anderson, James M. ;
Rodriguez, Analiz ;
Chang, David T. .
SEMINARS IN IMMUNOLOGY, 2008, 20 (02) :86-100
[7]  
[Anonymous], 2006, NUCL ACIDS S SERIES, DOI DOI 10.1093/nass/nrl016
[8]   SITE-SPECIFIC INCORPORATION OF NONNATURAL RESIDUES DURING INVITRO PROTEIN-BIOSYNTHESIS WITH SEMISYNTHETIC AMINOACYL-TRANSFER RNAS [J].
BAIN, JD ;
DIALA, ES ;
GLABE, CG ;
WACKER, DA ;
LYTTLE, MH ;
DIX, TA ;
CHAMBERLIN, AR .
BIOCHEMISTRY, 1991, 30 (22) :5411-5421
[9]   BIOSYNTHETIC SITE-SPECIFIC INCORPORATION OF A NON-NATURAL AMINO-ACID INTO A POLYPEPTIDE [J].
BAIN, JD ;
GLABE, CG ;
DIX, TA ;
CHAMBERLIN, AR ;
DIALA, ES .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1989, 111 (20) :8013-8014
[10]   Boron neutron capture therapy of cancer: Current status and future prospects [J].
Barth, RF ;
Coderre, JA ;
Vicente, MGH ;
Blue, TE .
CLINICAL CANCER RESEARCH, 2005, 11 (11) :3987-4002