Simplified Synthetic Antibody Libraries
Synthetic antibody libraries are constructed from scratch using designed synthetic DNA. Precise control over design enables the use of highly optimized human frameworks and the introduction of defined chemical diversity at positions that are most likely to contribute to antigen recognition. We descr...
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Veröffentlicht in: | Methods in Enzymology 2012, Vol.502, p.3-23 |
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creator | Rajan, Saravanan Sidhu, Sachdev S. |
description | Synthetic antibody libraries are constructed from scratch using designed synthetic DNA. Precise control over design enables the use of highly optimized human frameworks and the introduction of defined chemical diversity at positions that are most likely to contribute to antigen recognition. We describe complete methods for the design, construction, and application of simplified synthetic antibody libraries built on a single human framework with diversity restricted to four complementarity-determining regions and two amino acids (tyrosine and serine). Despite the extreme simplicity of design, these libraries are capable of generating specific antibodies against diverse protein antigens. Moreover, the same methods can be used to build more complex libraries that can produce synthetic antibodies with affinities and specificities beyond the scope of natural antibodies. Most importantly, these simplified methods rely on standard supplies, equipment, and methods that are accessible to any molecular biology laboratory. |
doi_str_mv | 10.1016/B978-0-12-416039-2.00001-X |
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Precise control over design enables the use of highly optimized human frameworks and the introduction of defined chemical diversity at positions that are most likely to contribute to antigen recognition. We describe complete methods for the design, construction, and application of simplified synthetic antibody libraries built on a single human framework with diversity restricted to four complementarity-determining regions and two amino acids (tyrosine and serine). Despite the extreme simplicity of design, these libraries are capable of generating specific antibodies against diverse protein antigens. Moreover, the same methods can be used to build more complex libraries that can produce synthetic antibodies with affinities and specificities beyond the scope of natural antibodies. 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All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c328t-c37056870e748c2fcc7ed243c535eed71cf4b5a6c73529874b462a2c6c38cc4f3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/B978-0-12-416039-2.00001-X$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,779,780,784,793,3457,3548,4022,11286,27921,27922,27923,45808,45993</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22208979$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Rajan, Saravanan</creatorcontrib><creatorcontrib>Sidhu, Sachdev S.</creatorcontrib><title>Simplified Synthetic Antibody Libraries</title><title>Methods in Enzymology</title><addtitle>Methods Enzymol</addtitle><description>Synthetic antibody libraries are constructed from scratch using designed synthetic DNA. Precise control over design enables the use of highly optimized human frameworks and the introduction of defined chemical diversity at positions that are most likely to contribute to antigen recognition. We describe complete methods for the design, construction, and application of simplified synthetic antibody libraries built on a single human framework with diversity restricted to four complementarity-determining regions and two amino acids (tyrosine and serine). Despite the extreme simplicity of design, these libraries are capable of generating specific antibodies against diverse protein antigens. Moreover, the same methods can be used to build more complex libraries that can produce synthetic antibodies with affinities and specificities beyond the scope of natural antibodies. Most importantly, these simplified methods rely on standard supplies, equipment, and methods that are accessible to any molecular biology laboratory.</description><subject>Amino Acid Sequence</subject><subject>Amino Acids - genetics</subject><subject>Amino Acids - immunology</subject><subject>Antibodies - chemistry</subject><subject>Antibodies - genetics</subject><subject>Antibodies - immunology</subject><subject>Antibodies - metabolism</subject><subject>Antibody Affinity - immunology</subject><subject>Antigens - genetics</subject><subject>Antigens - immunology</subject><subject>Antigens - metabolism</subject><subject>Bacteriophages - chemistry</subject><subject>Bacteriophages - genetics</subject><subject>Biotinylation</subject><subject>complementarity determining regions</subject><subject>Electroporation</subject><subject>ELISA</subject><subject>Enzyme-Linked Immunosorbent Assay</subject><subject>Escherichia coli</subject><subject>Humans</subject><subject>Models, Molecular</subject><subject>Molecular Sequence Data</subject><subject>oligonucleotide-directed mutagenesis</subject><subject>Peptide Library</subject><subject>Phage display libraries</subject><subject>phagemid</subject><subject>Plasmids - chemistry</subject><subject>Plasmids - genetics</subject><subject>Protein Engineering - methods</subject><subject>Sequence Analysis, DNA</subject><subject>synthetic antibodies</subject><subject>Transformation, Bacterial</subject><issn>0076-6879</issn><issn>1557-7988</issn><isbn>0124160395</isbn><isbn>9780124160392</isbn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo1kMlOwzAQhi0W0VL6Cqji0pOLlzi2j6WsUiUOBak3K5lMhFGWEqdIfXtcAnOYmcM3y_8TcsPZgjOe3t5ZbSijXNCEp0xaKhYsBqfbEzLmSmmqrTGn5JJxMRDqjIwZ0ylNjbYjMg3h8ziRKsMtuyAjIQQzVtsxmW98vat86bGYbQ5N_4G9h9my6X3eFofZ2udd1nkMV-S8zKqA0786Ie-PD2-rZ7p-fXpZLdcUpDB9zJqpeJShTgyIEkBjIRIJSirEQnMok1xlKWiphDU6yZNUZAJSkAYgKeWEzIe9u6792mPoXe0DYFVlDbb74CyXWkSNOpLXf-Q-r7Fwu87XWXdw_9oicD8AGP_99ti5AB4bwMJ3CL0rWu84c0eL3dFiF3vhBgOdcL8Wu638AXhVaZQ</recordid><startdate>2012</startdate><enddate>2012</enddate><creator>Rajan, Saravanan</creator><creator>Sidhu, Sachdev S.</creator><general>Elsevier Science & Technology</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>2012</creationdate><title>Simplified Synthetic Antibody Libraries</title><author>Rajan, Saravanan ; Sidhu, Sachdev S.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c328t-c37056870e748c2fcc7ed243c535eed71cf4b5a6c73529874b462a2c6c38cc4f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Amino Acid Sequence</topic><topic>Amino Acids - genetics</topic><topic>Amino Acids - immunology</topic><topic>Antibodies - chemistry</topic><topic>Antibodies - genetics</topic><topic>Antibodies - immunology</topic><topic>Antibodies - metabolism</topic><topic>Antibody Affinity - immunology</topic><topic>Antigens - genetics</topic><topic>Antigens - immunology</topic><topic>Antigens - metabolism</topic><topic>Bacteriophages - chemistry</topic><topic>Bacteriophages - genetics</topic><topic>Biotinylation</topic><topic>complementarity determining regions</topic><topic>Electroporation</topic><topic>ELISA</topic><topic>Enzyme-Linked Immunosorbent Assay</topic><topic>Escherichia coli</topic><topic>Humans</topic><topic>Models, Molecular</topic><topic>Molecular Sequence Data</topic><topic>oligonucleotide-directed mutagenesis</topic><topic>Peptide Library</topic><topic>Phage display libraries</topic><topic>phagemid</topic><topic>Plasmids - chemistry</topic><topic>Plasmids - genetics</topic><topic>Protein Engineering - methods</topic><topic>Sequence Analysis, DNA</topic><topic>synthetic antibodies</topic><topic>Transformation, Bacterial</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Rajan, Saravanan</creatorcontrib><creatorcontrib>Sidhu, Sachdev S.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><jtitle>Methods in Enzymology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Rajan, Saravanan</au><au>Sidhu, Sachdev S.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Simplified Synthetic Antibody Libraries</atitle><jtitle>Methods in Enzymology</jtitle><addtitle>Methods Enzymol</addtitle><date>2012</date><risdate>2012</risdate><volume>502</volume><spage>3</spage><epage>23</epage><pages>3-23</pages><issn>0076-6879</issn><eissn>1557-7988</eissn><isbn>0124160395</isbn><isbn>9780124160392</isbn><abstract>Synthetic antibody libraries are constructed from scratch using designed synthetic DNA. Precise control over design enables the use of highly optimized human frameworks and the introduction of defined chemical diversity at positions that are most likely to contribute to antigen recognition. We describe complete methods for the design, construction, and application of simplified synthetic antibody libraries built on a single human framework with diversity restricted to four complementarity-determining regions and two amino acids (tyrosine and serine). Despite the extreme simplicity of design, these libraries are capable of generating specific antibodies against diverse protein antigens. Moreover, the same methods can be used to build more complex libraries that can produce synthetic antibodies with affinities and specificities beyond the scope of natural antibodies. Most importantly, these simplified methods rely on standard supplies, equipment, and methods that are accessible to any molecular biology laboratory.</abstract><cop>United States</cop><pub>Elsevier Science & Technology</pub><pmid>22208979</pmid><doi>10.1016/B978-0-12-416039-2.00001-X</doi><tpages>21</tpages></addata></record> |
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subjects | Amino Acid Sequence Amino Acids - genetics Amino Acids - immunology Antibodies - chemistry Antibodies - genetics Antibodies - immunology Antibodies - metabolism Antibody Affinity - immunology Antigens - genetics Antigens - immunology Antigens - metabolism Bacteriophages - chemistry Bacteriophages - genetics Biotinylation complementarity determining regions Electroporation ELISA Enzyme-Linked Immunosorbent Assay Escherichia coli Humans Models, Molecular Molecular Sequence Data oligonucleotide-directed mutagenesis Peptide Library Phage display libraries phagemid Plasmids - chemistry Plasmids - genetics Protein Engineering - methods Sequence Analysis, DNA synthetic antibodies Transformation, Bacterial |
title | Simplified Synthetic Antibody Libraries |
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