Chemical Modifications of Nucleic Acid Aptamers for Therapeutic Purposes

被引:246
作者
Ni, Shuaijian [1 ,2 ]
Yao, Houzong [1 ,2 ]
Wang, Lili [1 ,2 ]
Lu, Jun [1 ,2 ]
Jiang, Feng [1 ,2 ,3 ]
Lu, Aiping [1 ,2 ]
Zhang, Ge [1 ,2 ]
机构
[1] HKBU, Sch Chinese Med, Inst Precis Med & Innovat Drug Discovery, Hong Kong 999077, Hong Kong, Peoples R China
[2] HKBU, Sch Chinese Med, Inst Adv Translat Med Bone & Joint Dis, Hong Kong 999077, Hong Kong, Peoples R China
[3] Ningbo Univ, Fac Mat Sci & Chem Engn, State Key Lab Base Novel Funct Mat & Preparat Sci, Ningbo 315211, Zhejiang, Peoples R China
关键词
nucleic acid aptamer; nuclease degradation; rapid excretion; binding affinity; chemical modification; IN-VITRO SELECTION; X-RAY DIFFRACTION; DNA APTAMERS; CRYSTAL-STRUCTURE; HIGH-AFFINITY; VASCULAR-PERMEABILITY; LYSOPHOSPHOLIPASE-D; ANTI-MUC1; APTAMER; BINDING RNA; STABILITY;
D O I
10.3390/ijms18081683
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
Nucleic acid aptamers have minimal immunogenicity, high chemical synthesis production, low cost and high chemical stability when compared with antibodies. However, the susceptibility to nuclease degradation, rapid excretion through renal filtration and insufficient binding affinity hindered their development as drug candidates for therapeutic applications. In this review, we will discuss methods to conquer these challenges and highlight recent developments of chemical modifications and technological advances that may enable early aptamers to be translated into clinical therapeutics.
引用
收藏
页数:21
相关论文
共 102 条
[1]   Evoking picomolar binding in RNA by a single phosphorodithioate linkage [J].
Abeydeera, N. Dinuka ;
Egli, Martin ;
Cox, Nehemiah ;
Mercier, Karen ;
Conde, Jonas Nascimento ;
Pallan, Pradeep S. ;
Mizurini, Daniella M. ;
Sierant, Malgorzata ;
Hibti, Fatima-Ezzahra ;
Hassell, Tom ;
Wang, Tianzhi ;
Liu, Feng-Wu ;
Liu, Hong-Min ;
Martinez, Carlos ;
Sood, Anil K. ;
Lybrand, Terry P. ;
Frydman, Chiraz ;
Monteiro, Robson Q. ;
Gomer, Richard H. ;
Nawrot, Barbara ;
Yang, Xianbin .
NUCLEIC ACIDS RESEARCH, 2016, 44 (17) :8052-8064
[2]   NMR monitoring of the SELEX process to confirm enrichment of structured RNA [J].
Amano, Ryo ;
Aoki, Kazuteru ;
Miyakawa, Shin ;
Nakamura, Yoshikazu ;
Kozu, Tomoko ;
Kawai, Gota ;
Sakamoto, Taiichi .
SCIENTIFIC REPORTS, 2017, 7
[3]   Six-SOMAmer Index Relating to Immune, Protease and Angiogenic Functions Predicts Progression in IPF [J].
Ashley, Shanna L. ;
Xia, Meng ;
Murray, Susan ;
O'Dwyer, David N. ;
Grant, Ethan ;
White, Eric S. ;
Flaherty, Kevin R. ;
Martinez, Fernando J. ;
Moore, Bethany B. .
PLOS ONE, 2016, 11 (08)
[4]   Aptamers as Both Drugs and Drug-Carriers [J].
Ashrafuzzaman, Md. .
BIOMED RESEARCH INTERNATIONAL, 2014, 2014
[5]   Discovery and development of the G-rich oligonucleotide AS1411 as a novel treatment for cancer [J].
Bates, Paula J. ;
Laber, Damian A. ;
Miller, Donald M. ;
Thomas, Shelia D. ;
Trent, John O. .
EXPERIMENTAL AND MOLECULAR PATHOLOGY, 2009, 86 (03) :151-164
[6]  
Beaucage S L, 2001, Curr Protoc Nucleic Acid Chem, VChapter 3, DOI 10.1002/0471142700.nc0303s00
[7]   Locked vs. unlocked nucleic acids (LNA vs. UNA): contrasting structures work towards common therapeutic goals [J].
Campbell, Meghan A. ;
Wengel, Jesper .
CHEMICAL SOCIETY REVIEWS, 2011, 40 (12) :5680-5689
[8]  
CARUTHERS MH, 1987, METHOD ENZYMOL, V154, P287
[9]   Synthesis of Readily Accessible Triazole-Linked Dimer Deoxynucleoside Phosphoramidite for Solid-Phase Oligonucleotide Synthesis [J].
Chandrasekhar, Srivari ;
Srihari, Pabbaraja ;
Nagesh, Chidalla ;
Kiranmai, Nayani ;
Nagesh, Narayana ;
Idris, M. Mohammed .
SYNTHESIS-STUTTGART, 2010, (21) :3710-3714
[10]   Expanding the application potential of DNA aptamers by their functionalization [J].
Chumakov, A. M. ;
Yuhina, E. S. ;
Frolova, E. I. ;
Kravchenko, J. E. ;
Chumakov, S. P. .
RUSSIAN JOURNAL OF BIOORGANIC CHEMISTRY, 2016, 42 (01) :1-13