{"title":"4.2 SPAAC和SPANC在生命科学中的应用","authors":"L. J. N. Janssen, D. Blanco‐Ania","doi":"10.1055/sos-sd-235-00184","DOIUrl":null,"url":null,"abstract":"The bioorthogonal, strain-promoted azide–alkyne cycloaddition (SPAAC) and the strain-promoted alkyne–nitrone cycloaddition (SPANC) reactions have been used for conjugation with high affinity and specificity. In contrast to the cytotoxic copper-catalyzed cycloaddition, both SPAAC and SPANC are inert in biological environments. This chapter reviews the developments and applications of SPAAC and SPANC in life sciences reported since 2004, when Bertozzi et al. published the first bioorthogonal reaction.","PeriodicalId":340057,"journal":{"name":"Click Chemistry","volume":"1960 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"1900-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"4.2 Applications of SPAAC and SPANC in Life Sciences\",\"authors\":\"L. J. N. Janssen, D. Blanco‐Ania\",\"doi\":\"10.1055/sos-sd-235-00184\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"The bioorthogonal, strain-promoted azide–alkyne cycloaddition (SPAAC) and the strain-promoted alkyne–nitrone cycloaddition (SPANC) reactions have been used for conjugation with high affinity and specificity. In contrast to the cytotoxic copper-catalyzed cycloaddition, both SPAAC and SPANC are inert in biological environments. This chapter reviews the developments and applications of SPAAC and SPANC in life sciences reported since 2004, when Bertozzi et al. published the first bioorthogonal reaction.\",\"PeriodicalId\":340057,\"journal\":{\"name\":\"Click Chemistry\",\"volume\":\"1960 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1900-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Click Chemistry\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1055/sos-sd-235-00184\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Click Chemistry","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1055/sos-sd-235-00184","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
4.2 Applications of SPAAC and SPANC in Life Sciences
The bioorthogonal, strain-promoted azide–alkyne cycloaddition (SPAAC) and the strain-promoted alkyne–nitrone cycloaddition (SPANC) reactions have been used for conjugation with high affinity and specificity. In contrast to the cytotoxic copper-catalyzed cycloaddition, both SPAAC and SPANC are inert in biological environments. This chapter reviews the developments and applications of SPAAC and SPANC in life sciences reported since 2004, when Bertozzi et al. published the first bioorthogonal reaction.
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