共 164 条
Aptamers targeting amyloidogenic proteins and their emerging role in neurodegenerative diseases
被引:22
作者:

Murakami, Kazuma
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h-index: 0
机构:
Kyoto Univ, Grad Sch Agr, Div Food Sci & Biotechnol, Kyoto, Japan Kyoto Univ, Grad Sch Agr, Div Food Sci & Biotechnol, Kyoto, Japan

Izuo, Naotaka
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h-index: 0
机构:
Univ Toyama, Fac Pharmaceut Sci, Lab Pharmaceut Therapy & Neuropharmacol, Toyama, Japan Kyoto Univ, Grad Sch Agr, Div Food Sci & Biotechnol, Kyoto, Japan

Bitan, Gal
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机构:
Univ Calif Los Angeles, David Geffen Sch Med, Brain Res Inst, Dept Neurol, Los Angeles, CA 90095 USA
Univ Calif Los Angeles, Mol Biol Inst, Los Angeles, CA 90095 USA Kyoto Univ, Grad Sch Agr, Div Food Sci & Biotechnol, Kyoto, Japan
机构:
[1] Kyoto Univ, Grad Sch Agr, Div Food Sci & Biotechnol, Kyoto, Japan
[2] Univ Toyama, Fac Pharmaceut Sci, Lab Pharmaceut Therapy & Neuropharmacol, Toyama, Japan
[3] Univ Calif Los Angeles, David Geffen Sch Med, Brain Res Inst, Dept Neurol, Los Angeles, CA 90095 USA
[4] Univ Calif Los Angeles, Mol Biol Inst, Los Angeles, CA 90095 USA
关键词:
CELLULAR PRION PROTEIN;
NUCLEIC-ACID APTAMERS;
IN-VITRO SELECTION;
RNA APTAMER;
ALPHA-SYNUCLEIN;
DNA APTAMERS;
ALZHEIMERS-DISEASE;
WEB SERVER;
QUADRUPLEX STRUCTURE;
MESSENGER-RNAS;
D O I:
10.1016/j.jbc.2021.101478
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:
Aptamers are oligonucleotides selected from large pools of random sequences based on their affinity for bioactive molecules and are used in similar ways to antibodies. Aptamers provide several advantages over antibodies, including their small size, facile, large-scale chemical synthesis, high stability, and low immunogenicity. Amyloidogenic proteins, whose aggregation is relevant to neurodegenerative diseases, such as Alzheimer's, Parkinson's, and prion diseases, are among the most challenging targets for aptamer development due to their conformational instability and heterogeneity, the same characteristics that make drug development against amyloidogenic proteins difficult. Recently, chemical tethering of aptagens (equivalent to antigens) and advances in high-throughput sequencing-based analysis have been used to overcome some of these challenges. In addition, internalization technologies using fusion to cellular receptors and extracellular vesicles have facilitated central nervous system (CNS) aptamer delivery. In view of the development of these techniques and resources, here we review antiamyloid aptamers, highlighting preclinical application to CNS therapy.
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