Difference between revisions of "Team:SDU-Denmark/Tour72"

 
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<h2> Medical aspects </h2>
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<p> <i> "If I have seen further it is by standing on the shoulders of Giants" - <b>Sir Isaac Newton</b></i></p>
<p class="intro"> Although there is no doubt that peptide aptamers are potential tivals of traditional antibodies in medicine and therapy, some challenges have to accomodated before they can be implemented clinically. </p>
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<h3> Size of the peptide </h3>
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<h1 align="center"> Medical aspects </h1>
<p> <span class="intro"> The bigger molecule the larger risk of immunogenicity. </span> To avoid an respons from the human immune system it is important that the peptide is as small as possible. If the immune system develops immunization against the peptide aptamer it will not have any function at all. </p>
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<h3> Effector mechanism </h3>
 
<p> <span class="intro"> Traditional antibodies have a Fab region</span>, that bind to microbes of which they have specificity. Activation of the immune respons is conducted through their Fc region that interacts with Fc receptors on cell surfaces of lymphocytes and/or other effector cells of the immune system. </p>
 
<h3> Half-life </h3>
 
  
<p> <span class="intro"> Peptide aptamers targeted at chronic diseases </span>have to have a very long degradation time. </p>
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<div class="thumb tright">
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<div class="thumbinner" style="width:235px; height:280px;">
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<a class="popupImg alignRight" style="width:230px" target="_blank" href="https://static.igem.org/mediawiki/2015/e/eb/SDU2015_Immunoglobulin.png" title="1: Fab region, 2: Fc region, 3: Heavy chain, 4: Light chain, 5: Antigen binding site (paratope), 6: Hinge regions.">
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  <img src="https://static.igem.org/mediawiki/2015/9/95/Immunoglobulin_basic_unit_thumbnail.png" style="width:230px"/></a>
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<div class="thumbcaption">Figure 1: The structure of an immunoglobulin (Ig) </div>
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</div>
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</div>
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<p> <span class="intro">Antibodies, immunoglobulins, are proteins</span> that bind targets ('antigens'). They are produced in vertebrates as a defense against foreign microbes.
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This characteristic has been utilized in research for decades. As mentioned in the introduction, monoclonal antibodies (mAbs) are frequently used for numerous purposes in research and in medical aspects.       
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</p>
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<p> <span class="intro"> For peptide aptamers</span> to be implementable in diagnostics and therapy, some challenges have to be accomodated. Antibodies comprise a dangerous threat for microorganisms displaying pathogen-associated molecular patterns (PAMPs). PAMPs are recognized by the antibodies <span class="tooltipLink">Fab</span><span class="tooltip"><span class="tooltipHeader">Fab</span>fragment, antigen-binding</span>-region and induces an immune response through the <span class="tooltipLink">Fc</span><span class="tooltip"><span class="tooltipHeader">Fc</span>fragment, crystallizable</span>-region, that binds effector cells of the immune system. The effector mechanisms include: <span class="tooltipLink">Opsonisation</span><span class="tooltip"><span class="tooltipHeader">Opsonisation</span><i>Opson</i> originates from Grece, where it referrers to a delicious side-dish. In this context it means that antibodies mark pathogens, making them more appetizing for phagocytes (i.e. neutrophils and macrophages)</span>, <span class="tooltipLink">agglutination</span><span class="tooltip"><span class="tooltipHeader">Agglutination</span><i>Agglutinare</i> is Latin and means "to glue". In the immune response it means that the antibodies bind multiple antigens, creating a cluster which is easier for the phagocytes to process in one portion instead of one by one.</span> and <span class="tooltipLink">complement activation</span><span class="tooltip"><span class="tooltipHeader">Complement System</span>When the system is activated, several proteases begin to cleave proteins that release certain cytokines, toxic to the pathogen. By a cascade of cleavage reactions the result is the production of a so called <i>cell killing membrane attack complex</i> that will destroy the given microbe.</span> among other reactions.
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</p> 
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<p>
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<span class="intro"> One example of an </span>effector mechanism could be to attach small gold nanoparticles (sAuNPs). sAuNPs have recently shown to be excellent tools for cancer therapy, especially because of their high biocompatibily, large surface-to-volume ratio and strong diffusivit<span class="sourceReference">y</span>, which ensure that they remain intact while moving through organisms e.g. 
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<span class="tooltip">
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  <span class="tooltipHeader">Reference:</span>
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    Kim CS, et al. Cellular imaging of endosome entrapped small gold nanoparticles, 2015 Jun 10;2:306-15. doi: 10.1016/j.mex.2015.06.001. <a target="blank_" href="http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4487928/">[PubMed]</a>
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</span>
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By attaching sAuNPs to a peptide aptamer it would be possible to detect and attack pathogenic organisms more precisely, such as cancer cells, instead of using the current method of targeted radioactive therapy where adjacent normal tissue can be seriously damaged <span class="sourceReference">too</span>.
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<span class="tooltip">
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  <span class="tooltipHeader">Reference:</span>
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    Thorek DL et al. Reverse-Contrast Imaging and Targeted Radiation Therapy of Advanced Pancreatic Cancer Models. Int J Radiat Oncol Biol Phys. 2015 Jun 9. pii: S0360-3016(15)00612-4. <br> doi:10.1016/j.ijrobp.2015.06.001  <a target="blank_" href="http://www.ncbi.nlm.nih.gov/pubmed/26238952">[PubMed]
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</a>
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<br>
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<br>
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Chan MD. Recent Technical Advances and Indications for Radiation Therapy in Low-Grade Glioma. Semin Radiat Oncol. 2015 Jul;25(3):189-96. <br>doi: 10.1016/j.semradonc.2015.02.001
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<a href="http://www.ncbi.nlm.nih.gov/pubmed/?term=Recent+Technical+Advances+and+Indications+for+Radiation+Therapy+in+Low-Grade+Glioma" target="_blank">[PubMed]</a>
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</span> 
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If peptide aptamers were to be used as tools in cancer therapy it would be necessary for them to be tolerated by the immune system and show high level of specificity.
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</p>
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<p>
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<span class="intro"> One chance of </span>being tolerated by the immune system is by adjusting the size of the protein. The bigger the molecule the larger risk of <span class="tooltipLink">immunogenicity</span><span class="tooltip"><span class="tooltipHeader">Immunogenicity</span>If a organism or substance i immunogenic it means that it is able to provoke an response from the human immune system.</span>. If the immune system develops immunization against the peptide aptamer it will not have any function.   
 +
Today, most often mammalian cells are used for production of mAbs, primarily because of their ability to perform post-translational modifications (PTM). Especially N-glycosylation is an important step, resulting in avoidance of the human immune system, i.e. minimizing the risk of immunogenicity. <i> E. coli</i> does not have these specifications yet back in 2002 researches found an N-linked glycosylation system in the bacterium Campylobacter jejuni and demonstrated that a functional N-linked glycosylation pathway could be transferred into <i>E. coli</i> <span class="sourceReference">too</span>.
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<span class="tooltip">
 +
  <span class="tooltipHeader">Reference:</span>
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    Wacker M et al. N-linked glycosylation in Campylobacter jejuni and its functional transfer into E. coli. Science. 2002 Nov 29;298(5599):1790-3. <a target="blank_" href="http://www.ncbi.nlm.nih.gov/pubmed/12459590">[PubMed]
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</a>
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</span>
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</p>
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<p>
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<span class="intro">Another important</span> aspetc is the peptide aptamers half-life. To be able to should function as treatment for chronic and autoimmune diseases, such as rheumatoid arthritis and multiple sclerosis and disseminated sclerosis, the half-life should be adjustable. Read more about the half-life of our peptide aptamer in <a href="https://2015.igem.org/Team:SDU-Denmark/Tour23">The Alternative</a>. 
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</p>
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<p>
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<span class="intro">Specificity and quality control</span> are some of the most controversial topics regarding the use of antibodies. How can one demonstrate that a given antibody have specificity for a antigen and not anything ells. That would require the researcher to out think any possible substance that the antibody hypothetically could bind and test it - i.e. it is not possible. Yet our peptide aptamer has just as high specificity as antibodies (see table 1, <a href="https://2015.igem.org/Team:SDU-Denmark/Tour23">The Alternative</a>). Other comparisons are schematized in <a href="#Table1">Table 1</a> underneath this section.
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</p>
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<p>
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<table id="Table1" class="wikitable" style="width:90%;"><caption><b>Table 1:</b> Monoclonal Antibodies vs Small Molecu<span class="sourceReference">les</span>.
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<span class="tooltip">
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  <span class="tooltipHeader">Reference:</span>
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    Silberstein S, Lenz R, Xu C. Therapeutic Monoclonal Antibodies: What Headache Specialists Need to Know. Headache. 2015 Aug 28. doi: 10.1111/head.12642. <a target="blank_" href="http://www.ncbi.nlm.nih.gov/pubmed/26316307">[PubMed]
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</a>
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</span>
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</caption>
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<tr><td></td><td><b>Monoclonal antibodies</b></td><td><b>Small molecules</b> (e.g. peptide aptamers)</td></tr>
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<tr><td> <b>Target specificity</b></td><td> High</td><td>Low</td></tr>
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<tr><td> <b>Size</b></td><td>High molecular weight (~150kD)</td><td> Low molecular weigth </td></tr>
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<tr><td> <b>Targets</b></td><td>Extracellular</td><td>Intracellular/extracellular</td></tr>
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<tr><td> <b>Crosses Blood-Brain Barrier</b></td><td> No </td><td> Possibly</td></tr>
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</table>
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</p>
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<p>
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Even though small molecules are less target specific compared to mAbs their characteristics can be beneficial; they can attack multiple targets, they most possibly have the ability to cross the Blood-Brain Barrier (BBB) and thereby function as therapy against malignant brain tumors and other intercerebral and neurological diseases. 
 +
</p>
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<p>
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<span class="intro"> Despite</span> these challenges and possibly other obstacles, the use of peptide aptamers in the future seems promising.  
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</p>
 
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Latest revision as of 00:31, 19 September 2015

"If I have seen further it is by standing on the shoulders of Giants" - Sir Isaac Newton

Medical aspects

Figure 1: The structure of an immunoglobulin (Ig)

Antibodies, immunoglobulins, are proteins that bind targets ('antigens'). They are produced in vertebrates as a defense against foreign microbes. This characteristic has been utilized in research for decades. As mentioned in the introduction, monoclonal antibodies (mAbs) are frequently used for numerous purposes in research and in medical aspects.

For peptide aptamers to be implementable in diagnostics and therapy, some challenges have to be accomodated. Antibodies comprise a dangerous threat for microorganisms displaying pathogen-associated molecular patterns (PAMPs). PAMPs are recognized by the antibodies FabFabfragment, antigen-binding-region and induces an immune response through the FcFcfragment, crystallizable-region, that binds effector cells of the immune system. The effector mechanisms include: OpsonisationOpsonisationOpson originates from Grece, where it referrers to a delicious side-dish. In this context it means that antibodies mark pathogens, making them more appetizing for phagocytes (i.e. neutrophils and macrophages), agglutinationAgglutinationAgglutinare is Latin and means "to glue". In the immune response it means that the antibodies bind multiple antigens, creating a cluster which is easier for the phagocytes to process in one portion instead of one by one. and complement activationComplement SystemWhen the system is activated, several proteases begin to cleave proteins that release certain cytokines, toxic to the pathogen. By a cascade of cleavage reactions the result is the production of a so called cell killing membrane attack complex that will destroy the given microbe. among other reactions.

One example of an effector mechanism could be to attach small gold nanoparticles (sAuNPs). sAuNPs have recently shown to be excellent tools for cancer therapy, especially because of their high biocompatibily, large surface-to-volume ratio and strong diffusivity, which ensure that they remain intact while moving through organisms e.g. Reference: Kim CS, et al. Cellular imaging of endosome entrapped small gold nanoparticles, 2015 Jun 10;2:306-15. doi: 10.1016/j.mex.2015.06.001. [PubMed] By attaching sAuNPs to a peptide aptamer it would be possible to detect and attack pathogenic organisms more precisely, such as cancer cells, instead of using the current method of targeted radioactive therapy where adjacent normal tissue can be seriously damaged too. Reference: Thorek DL et al. Reverse-Contrast Imaging and Targeted Radiation Therapy of Advanced Pancreatic Cancer Models. Int J Radiat Oncol Biol Phys. 2015 Jun 9. pii: S0360-3016(15)00612-4.
doi:10.1016/j.ijrobp.2015.06.001 [PubMed]

Chan MD. Recent Technical Advances and Indications for Radiation Therapy in Low-Grade Glioma. Semin Radiat Oncol. 2015 Jul;25(3):189-96.
doi: 10.1016/j.semradonc.2015.02.001 [PubMed]
If peptide aptamers were to be used as tools in cancer therapy it would be necessary for them to be tolerated by the immune system and show high level of specificity.

One chance of being tolerated by the immune system is by adjusting the size of the protein. The bigger the molecule the larger risk of immunogenicityImmunogenicityIf a organism or substance i immunogenic it means that it is able to provoke an response from the human immune system.. If the immune system develops immunization against the peptide aptamer it will not have any function. Today, most often mammalian cells are used for production of mAbs, primarily because of their ability to perform post-translational modifications (PTM). Especially N-glycosylation is an important step, resulting in avoidance of the human immune system, i.e. minimizing the risk of immunogenicity. E. coli does not have these specifications yet back in 2002 researches found an N-linked glycosylation system in the bacterium Campylobacter jejuni and demonstrated that a functional N-linked glycosylation pathway could be transferred into E. coli too. Reference: Wacker M et al. N-linked glycosylation in Campylobacter jejuni and its functional transfer into E. coli. Science. 2002 Nov 29;298(5599):1790-3. [PubMed]

Another important aspetc is the peptide aptamers half-life. To be able to should function as treatment for chronic and autoimmune diseases, such as rheumatoid arthritis and multiple sclerosis and disseminated sclerosis, the half-life should be adjustable. Read more about the half-life of our peptide aptamer in The Alternative.

Specificity and quality control are some of the most controversial topics regarding the use of antibodies. How can one demonstrate that a given antibody have specificity for a antigen and not anything ells. That would require the researcher to out think any possible substance that the antibody hypothetically could bind and test it - i.e. it is not possible. Yet our peptide aptamer has just as high specificity as antibodies (see table 1, The Alternative). Other comparisons are schematized in Table 1 underneath this section.

Table 1: Monoclonal Antibodies vs Small Molecules. Reference: Silberstein S, Lenz R, Xu C. Therapeutic Monoclonal Antibodies: What Headache Specialists Need to Know. Headache. 2015 Aug 28. doi: 10.1111/head.12642. [PubMed]
Monoclonal antibodiesSmall molecules (e.g. peptide aptamers)
Target specificity HighLow
SizeHigh molecular weight (~150kD) Low molecular weigth
TargetsExtracellularIntracellular/extracellular
Crosses Blood-Brain Barrier No Possibly

Even though small molecules are less target specific compared to mAbs their characteristics can be beneficial; they can attack multiple targets, they most possibly have the ability to cross the Blood-Brain Barrier (BBB) and thereby function as therapy against malignant brain tumors and other intercerebral and neurological diseases.

Despite these challenges and possibly other obstacles, the use of peptide aptamers in the future seems promising.