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[[File:Aptamer biotin.png|thumb|Structure of an RNA aptamer specific for [[biotin]]. The aptamer surface and backbone are shown in yellow. Biotin (spheres) fits snugly into a cavity of the RNA surface]]
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'''Aptamers'''  (from the Latin ''aptus'' - fit, and Greek ''meros'' - part) are [[oligonucleotide|oligonucleic acid]] or [[peptide]] molecules that bind to a specific target molecule.  Aptamers are usually created by selecting them from a large random [[Sequencing|sequence]] pool, but natural aptamers also exist in [[riboswitch]]es.  Aptamers can be used for both basic research and clinical purposes as macromolecular drugs.  Aptamers can be combined with [[ribozyme]]s to self-cleave in the presence of their target molecule.  These compound molecules have additional research, industrial and clinical applications.


More specifically, aptamers can be classified as:
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* [[Deoxyribonucleic acid|DNA]] or [[ribonucleic acid|RNA]] or [[Nucleic acid analogues|XNA]] aptamers. They consist of (usually short) strands of oligonucleotides.
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* [[Peptide]] aptamers. They consist of a short variable peptide domain, attached at both ends to a protein scaffold.
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==Nucleic Acid aptamers==
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Nucleic acid aptamers are [[nucleic acid]] species that have been engineered through repeated rounds of ''in vitro [[selection]]'' or equivalently, SELEX ([[systematic evolution of ligands by exponential enrichment]]) to bind to various molecular targets such as small molecules, proteins, nucleic acids, and even cells, tissues and organisms.  Aptamers are useful in [[biotechnology|biotechnological]] and therapeutic applications as they offer molecular recognition properties that rival that of the commonly used biomolecule, [[antibody|antibodies]].  In addition to their discriminate recognition, aptamers offer advantages over antibodies as they can be engineered completely in a test tube, are readily produced by chemical synthesis, possess desirable storage properties, and elicit little or no [[immunogenicity]] in therapeutic applications.


In 1990, two labs independently developed the technique of selection: the Gold lab, using the term SELEX for their process of selecting RNA [[ligand (biochemistry)|ligands]] against T4 [[DNA polymerase]]; and the Szostak lab, coining the term ''in vitro selection'', selecting RNA ligands against various organic dyes. The Szostak lab also coined the term aptamer (from the Latin, ''apto'', meaning ‘to fit’) for these nucleic acid-based ligands. Two years later, the Szostak lab and [[Gilead Sciences]], independent of one another, used ''in vitro selection'' schemes to evolve single stranded DNA ligands for organic dyes and human coagulant, thrombin, respectively. There does not appear to be any systematic differences between RNA and DNA aptamers, save the greater intrinsic chemical stability of DNA.
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Interestingly enough, the notion of selection ''in vitro'' was actually preceded twenty-plus years prior when [[Sol Spiegelman]] used a [[Bacteriophage Qβ|Qbeta]] replication system as a way to evolve a self-replicating molecule.<ref>{{cite journal|last=Mills|first=DR|coauthors=Peterson, RL; Spiegelman, S|title=An extracellular Darwinian experiment with a self-duplicating nucleic acid molecule.|journal=Proceedings of the National Academy of Sciences of the United States of America|date=July 1967|volume=58|issue=1|pages=217–24|pmid=5231602}}</ref>  In addition, a year before the publishing of ''in vitro selection'' and SELEX, [[Gerald Joyce]] used a system that he termed ‘directed evolution’ to alter the cleavage activity of a ribozyme.
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Since the discovery of aptamers, many researchers have used aptamer selection as a means for application and discovery.  In 2001, the process of ''in vitro selection'' was automated<ref name="Cox2001">{{Cite pmid|11557339}}</ref><ref name="Cox2002a">{{Cite pmid|12052180}}</ref><ref name="Cox2002b">{{Cite pmid|12384610}}</ref> by J. Colin Cox in the Ellington lab at the [[University of Texas at Austin]], and at [[SomaLogic]], Inc (Boulder, CO), reducing the duration of a selection experiment from six weeks to three days.
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While the process of artificial engineering of nucleic acid ligands is highly interesting to biology and biotechnology, the notion of aptamers in the natural world had yet to be uncovered until 2002 when two groups led by [[Ronald Breaker]] and Evgeny Nudler discovered a nucleic acid-based genetic regulatory element (which was named [[riboswitch]]) that possesses similar molecular recognition properties to the artificially made aptamers.  In addition to the discovery of a new mode of genetic regulation, this adds further credence to the notion of an ‘[[RNA world hypothesis|RNA World]],’ a postulated stage in time in the origins of life on Earth.
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Both DNA and RNA aptamers show robust binding affinities for various targets.<ref>{{cite journal|last=Neves|first=M.A.D.|coauthors=O. Reinstein, M.Saad, P.E. Johnson|title=Defining the secondary structural requirements of a cocaine-binding aptamer by a thermodynamic and mutation study|journal=Biophys Chem|year=2010|volume=153|pages=9–16|pmid=21035241|doi=10.1016/j.bpc.2010.09.009}}</ref><ref>{{cite journal|last=Baugh|first=C.|coauthors=D. Grate, C.Wilson|title=2.8 angstrom crystal structure of the malachite green aptamer.|journal=J. Mol. Biol.|year=2000|volume=301|pages=117–128|pmid=10926496|doi=10.1006/jmbi.2000.3951}}</ref><ref>{{cite journal|last=Dieckmann|first=T.|coauthors=E. Fujikawa, X. Xhao, J. Szostak, J. Feigon|title=Structural Investigations of RNA and DNA aptamers in Solution|journal=Journal of Cellular Biochemistry|year=1995|pages=56-56}}</ref> DNA and RNA aptamers have been selected for the same target. These targets include [[lysozyme]],<ref>{{cite journal|last=Potty|first=A.|coauthors=K. Kourentzi, H. Fang, G. Jackson, X. Zhang, G. Legge, R. Willson|title=Biophysical Characterization of DNA Aptamer Interactions with Vascular Endothelial Growth Factor.|journal=Biopolymers|year=2009|volume=91|pages=145–156|pmid=19025993|doi=10.1002/bip.21097}}</ref> [[thrombin]],<ref>{{cite journal|last=Long|first=S.|coauthors=M. Long, R. White, B. Sullenger|title=Crystal structure of an RNA aptamer bound to thrombin|journal=RNA|year=2008|volume=14|pages=2504–2512|pmid=18971322|issue=2|doi=10.1261/rna.1239308|pmc=2590953}}</ref> human immunodeficiency virus trans-acting responsive element (HIV TAR),<ref>{{cite journal|last=Darfeuille|first=F.|coauthors=S. Reigadas, J. Hansen, H. Orum, C. Di Primo, J. Toulme|title=Aptamers targeted to an RNA hairpin show improved specificity compared to that of complementary oligonucleotides.|journal=Biochemistry|year=2006|volume=45|pages=12076–12082|pmid=17002307|doi=10.1021/bi0606344}}</ref> [[hemin]],<ref>{{cite journal|last=Liu|first=M.|coauthors=T. Kagahara, H. Abe, Y. Ito|title=Direct In Vitro Selection of Hemin-Binding DNA Aptamer with Peroxidase Activity|journal=Bulletin of the Chemical Society of Japan|year=2009|volume=82|pages=99–104}}</ref> [[interferon γ]],<ref>{{cite journal|last=Min|first=K.|coauthors=M. Cho, S. Han, Y. Shim, J. Ku, C. Ban|title=A simple and direct electrochemical detection of interferon-gamma using its RNA and DNA aptamers.|journal=Biosensors & Bioelectronics|year=2008|volume=23|pages=1819–1824|pmid=18406597|doi=10.1016/j.bios.2008.02.021}}</ref> [[vascular endothelial growth factor]] (VEGF),<ref>{{cite journal|last=Ng|first=E.W.M|coauthors=D.T. Shima, P. Calias, E.T. Cunningham, D.R. Guyer, A.P. Adamis|title=Pegaptanib, a targeted anti-VEGF aptamer for ocular vascular disease.|journal=Nature Reviews Drug Discovery|year=2006|volume=5|pages=123–132|pmid=16518379|doi=10.1038/nrd1955|issue=2}}</ref> [[prostate specific antigen]] (PSA),<ref>{{cite journal|last=Savory|first=N.|coauthors=K. Abe, K. Sode, K. Ikebukuro|title=Selection of DNA aptamer against prostate specific antigen using a genetic algorithm and application to sensing.|journal=Biosensors & Bioelectronics|year=2010|volume=15|pages=1386-91|pmid= 20692149 |doi=10.1016/j.bios.2010.07.057}}</ref> <ref>{{cite journal|last=Jeong |first=S.|coauthors=S.R. Han, Y.J. Lee, S.W. Lee|title=Selection of RNA aptamers specific to active prostate-specific antigen.|journal=Biotechnology Letters|year=2010|volume=32|pages=379-85|pmid= 19943183 |doi=10.1007/s10529-009-0168-1}}</ref>and [[dopamine]].<ref>{{cite journal|last=Walsh|first=R.|coauthors=M. DeRosa|title=Retention of function in the DNA homolog of the RNA dopamine aptamer.|journal=Biochemical and Biophysical Research Communications|year=2009|volume=388|pages=732–735|pmid=19699181|doi=10.1016/j.bbrc.2009.08.084}}</ref> In the case of lysozyme, HIV TAR, VEGF and dopamine the DNA aptamer is the analog of the RNA aptamer, with thymine replacing uracil. The hemin, thrombin, and interferon γ, DNA and RNA aptamers were selected through independent selections and have unique sequences. Considering that not all DNA analogs of RNA aptamers show functionality the correlation between DNA and RNA sequence and their structure and function requires further investigation.
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Lately, a concept of [[smart aptamers]], and [[smart ligands]] in general, has been introduced. It describes aptamers that are selected with pre-defined equilibrium (<math>K_{d}</math>), rate (<math>k_{off}</math>, <math>k_{on}</math>) constants and thermodynamic (ΔH, ΔS) parameters of aptamer-target interaction. [[Kinetic capillary electrophoresis]] is the technology used for the selection of smart aptamers. It obtains aptamers in a few rounds of selection.
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Recent developments in aptamer-based therapeutics have been rewarded in the form of the first aptamer-based drug approved by the U.S. [[Food and Drug Administration]] (FDA) in treatment for [[age-related macular degeneration]] (AMD), called [[Macugen]] offered by [[OSI Pharmaceuticals]]. In addition, the company NeoVentures Biotechnology Inc. (http://www.neoventures.ca) has successfully commercialized the first aptamer based diagnostic platform for analysis of mycotoxins in grain. Many contract companies develop aptamers and aptabodies to replace antibodies in research, diagnostic platforms, drug discovery, and therapeutics.
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Non-modified aptamers are cleared rapidly from the bloodstream, with a half-life of minutes to hours, mainly due to [[nuclease]] degradation and clearance from the body by the kidneys, a result of the  aptamer's inherently low molecular weight.  Unmodified aptamer applications currently focus on treating transient conditions such as blood clotting, or treating organs such as the eye where local delivery is possible.  This rapid clearance can be an advantage in applications such as ''in vivo'' diagnostic imaging.  An example is a tenascin-binding aptamer under development by [[Schering AG]] for cancer imaging.  Several modifications, such as 2'-fluorine-substituted [[pyrimidines]], [[polyethylene glycol]] (PEG) linkage, etc. (both of which are used in Macugen, an FDA-approved aptamer) are available to scientists with which to increase the serum [[half-life]] of aptamers easily to the day or even week time scale.
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Another approach to increase the nuclease resistance of aptamers is to develop [[Spiegelmer]]s, which are composed entirely of an unnatural L-ribonucleic acid backbone. A spiegelmer of the same sequence has the same binding properties of the corresponding RNA aptamer, except it binds to the mirror image of its target molecule.
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In addition to the development of aptamer-based therapeutics, many researchers such as the Ellington lab and independently another company SomaLogic (Boulder, CO) have been developing diagnostic techniques for aptamer based plasma protein profiling called [[aptamer plasma proteomics]].  This technology will enable future multi-biomarker protein measurements that can aid diagnostic distinction of disease versus healthy states.  Somalogic aptamers to HER2 and EGFR membrane proteins have also been demonstrated to work in the context of rapid frozen tissue intraoperative diagnostic pathology applications.<ref name=pmid21217521>{{cite journal |author= Gupta S, Thirstrup D, Jarvis TC, Schneider DJ, Wilcox SK, Carter J, Zhang C, Gelinas A, Weiss A, Janjic N, Baird GS. |title=Rapid Histochemistry Using Slow Off-rate Modified Aptamers With Anionic Competition.  |journal=Applied Immunohistochemistry & Molecular Morphology |volume=19 |issue=1 |pages=Epub ahead of print |date=Jan 2011 |pmid=21217521 |doi=10.1097/PAI.0b013e3182008c29 }}</ref>
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As a resource for all ''in vitro selection'' and SELEX experiments, the Ellington lab has developed the [[Aptamer Database]] cataloging all published experiments. This is found at http://aptamer.icmb.utexas.edu/.
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==Peptide aptamers==
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Peptide aptamers are proteins that are designed to interfere with other [[protein-protein interaction|protein interaction]]s inside cells. They consist of a variable peptide loop attached at both ends to a protamersein scaffold. This double structural constraint greatly increases the binding affinity of the peptide aptamer to levels comparable to an antibody's (nanomolar range).


The variable loop length is typically composed of ten to twenty [[amino acid]]s, and the scaffold may be any protein which has good [[solubility]] and [[compacity]] properties. Currently, the [[bacterial protein]] [[Thioredoxin]]-A is the most used scaffold protein, the variable loop being inserted within the reducing active site, which is a -Cys-Gly-Pro-Cys- loop in the wild protein, the two [[Cysteine]]s lateral chains being able to form a disulfide bridge.
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Peptide aptamer selection can be made using different systems, but the most used is currently the [[yeast]] [[two-hybrid system]].
<ul>
 
 
Selection of Ligand Regulated Peptide Aptamers (LiRPAs) has been demonstrated. By displaying 7 amino acid peptides from a novel [[scaffold protein]] based on the [[protein trimer|trimeric]] FKBP-rapamycin-FRB structure, interaction between the randomized peptide and target molecule can be controlled by the small molecule [[Rapamycin]] or non-immunosuppressive analogs.
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Peptide aptamer can also be selected from combinatorial peptide libraries constructed by [[phage display]] and other surface display technologies such as [[mRNA display]], [[ribosome display]], [[bacterial display]] and [[yeast display]]. These experimental procedures are also known as [[biopanning]]s. Among peptides obtained from biopannings, [[mimotope]]s can be considered as a kind of peptide aptamers. All the peptides panned from combinatorial peptide libraries have been stored in a special database with the name [[MimoDB]],<ref>{{cite journal|last=Huang|first=J|coauthors=Ru, B, Zhu, P, Nie, F, Yang, J, Wang, X, Dai, P, Lin, H, Guo, FB, Rao, N|title=MimoDB 2.0: a mimotope database and beyond.|journal=Nucleic Acids Research|date=2011-11-03|pmid=22053087|doi=10.1093/nar/gkr922|volume=40|issue=1|pages=D271–7|pmc=3245166}}</ref> which is freely available at http://immunet.cn/mimodb.
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==AptaBiD==
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AptaBiD or Aptamer-Facilitated Biomarker Discovery is a technology for [[biomarker]] discovery.<ref name=pmid18558676>{{cite journal |author=Berezovski MV, Lechmann M, Musheev MU, Mak TW, Krylov SN |title=Aptamer-facilitated biomarker discovery (AptaBiD) |journal=J Am Chem Soc. |volume=130 |issue=28 |pages=9137–43 |date=Jul 2008 |pmid=18558676 |doi=10.1021/ja801951p }}</ref> AptaBiD is based on multi-round generation of an aptamer or a pool of aptamers for differential molecular targets on the cells which facilitates exponential detection of biomarkers. It involves three major stages: (i) differential multi-round selection of aptamers for biomarker of target cells; (ii) aptamer-based isolation of biomarkers from target cells; and (iii) [[mass spectrometry]] identification of biomarkers. The important feature of the AptaBiD technology is that it produces synthetic affinity probes (aptamers) simultaneously with biomarker discovery. In AptaBiD, aptamers are developed for cell surface biomarkers in their native state and conformation. In addition to facilitating biomarker identification, such aptamers can be directly used for cell isolation, cell visualization, and tracking cells ''in vivo''. They can also be used to modulate activities of cell receptors and deliver different agents (e.g., [[small interfering RNA|siRNA]] and drugs) into the cells.
 
 
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==References==
 
{{reflist}}
  <li>[http://www.philatelie-france-russie.fr/spip.php?article51/ http://www.philatelie-france-russie.fr/spip.php?article51/]</li>
 
 
== Further reading ==
</ul>
{{refbegin}}
*{{cite journal |author=Ellington AD, Szostak JW |title=In vitro selection of RNA molecules that bind specific ligands |journal=Nature |volume=346 |issue=6287 |pages=818–22 |date=Aug 1990 |pmid=1697402 |doi=10.1038/346818a0 }}
*{{cite journal |author=Bock LC, Griffin LC, Latham JA, Vermaas EH, Toole JJ |title=Selection of single-stranded DNA molecules that bind and inhibit human thrombin |journal=Nature |volume=355 |issue=6360 |pages=564–6 |date=Feb 1992 |pmid=1741036 |doi=10.1038/355564a0 }}
*{{cite journal |author=Hoppe-Seyler F, Butz K |title=Peptide aptamers: powerful new tools for molecular medicine |journal=J Mol Med. |volume=78 |issue=8 |pages=426–30 |year=2000 |pmid=11097111 |url=http://link.springer.de/link/service/journals/00109/bibs/0078008/00780426.htm |doi=10.1007/s001090000140}}
*{{cite journal |author=Carothers JM, Oestreich SC, Davis JH, Szostak JW |title=Informational complexity and functional activity of RNA structures |journal=J Am Chem Soc. |volume=126 |issue=16 |pages=5130–7 |date=Apr 2004 |pmid=15099096 |doi=10.1021/ja031504a }}
*{{cite journal |author=Cohen BA, Colas P, Brent R |title=An artificial cell-cycle inhibitor isolated from a combinatorial library |journal=Proceedings of the National Academy of Sciences of the United States of America |volume=95 |issue=24 |pages=14272–7 |date=Nov 1998 |pmid=9826690 |pmc=24363 |url=http://www.pnas.org/cgi/pmidlookup?view=long&pmid=9826690 |doi=10.1073/pnas.95.24.14272}}
*{{cite journal |author=Binkowski BF, Miller RA, Belshaw PJ |title=Ligand-regulated peptides: a general approach for modulating protein-peptide interactions with small molecules |journal=Chem Biol. |volume=12 |issue=7 |pages=847–55 |date=Jul 2005 |pmid=16039531 |doi=10.1016/j.chembiol.2005.05.021 }}
*{{cite journal |author=Sullenger BA, Gilboa E |title=Emerging clinical applications of RNA |journal=Nature |volume=418 |issue=6894 |pages=252–8 |date=Jul 2002 |pmid=12110902 |doi=10.1038/418252a }}
*{{cite journal |author=Ng EW, Shima DT, Calias P, Cunningham ET, Guyer DR, Adamis AP |title=Pegaptanib, a targeted anti-VEGF aptamer for ocular vascular disease |journal=Nature Reviews Drug Discovery |volume=5 |issue=2 |pages=123–32 |date=Feb 2006 |pmid=16518379 |doi=10.1038/nrd1955 }}
*{{cite journal |author=Drabovich AP, Berezovski M, Okhonin V, Krylov SN |title=Selection of smart aptamers by methods of kinetic capillary electrophoresis |journal=Anal Chem. |volume=78 |issue=9 |pages=3171–8 |date=May 2006 |pmid=16643010 |doi=10.1021/ac060144h }}
*{{cite journal |author=Cho EJ, Lee JW, Ellington, AD |title=Applications of Aptamers as Sensors |journal=Annual Review of Analytical Chemistry |volume=2 |issue=1 |pages=241–64 |year=2009 |pmid=20636061 |url=http://arjournals.annualreviews.org/doi/abs/10.1146/annurev.anchem.1.031207.112851 |doi=10.1146/annurev.anchem.1.031207.112851}}
{{refend}}
 
==External links==
* [http://aptamer.freebase.com Aptamer - Freebase]
* [http://aptamerbase.semanticscience.org Aptamer Base]
* [http://immunet.cn/mimodb The MimoDB database]
 
[[Category:Nucleic acids]]
[[Category:Peptides]]
[[Category:Biotechnology]]
[[Category:Medical research]]

Revision as of 15:13, 7 February 2014

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