文献汇报课件.pptVIP

  1. 1、本文档共25页,可阅读全部内容。
  2. 2、有哪些信誉好的足球投注网站(book118)网站文档一经付费(服务费),不意味着购买了该文档的版权,仅供个人/单位学习、研究之用,不得用于商业用途,未经授权,严禁复制、发行、汇编、翻译或者网络传播等,侵权必究。
  3. 3、本站所有内容均由合作方或网友上传,本站不对文档的完整性、权威性及其观点立场正确性做任何保证或承诺!文档内容仅供研究参考,付费前请自行鉴别。如您付费,意味着您自己接受本站规则且自行承担风险,本站不退款、不进行额外附加服务;查看《如何避免下载的几个坑》。如果您已付费下载过本站文档,您可以点击 这里二次下载
  4. 4、如文档侵犯商业秘密、侵犯著作权、侵犯人身权等,请点击“版权申诉”(推荐),也可以打举报电话:400-050-0827(电话支持时间:9:00-18:30)。
  5. 5、该文档为VIP文档,如果想要下载,成为VIP会员后,下载免费。
  6. 6、成为VIP后,下载本文档将扣除1次下载权益。下载后,不支持退款、换文档。如有疑问请联系我们
  7. 7、成为VIP后,您将拥有八大权益,权益包括:VIP文档下载权益、阅读免打扰、文档格式转换、高级专利检索、专属身份标志、高级客服、多端互通、版权登记。
  8. 8、VIP文档为合作方或网友上传,每下载1次, 网站将根据用户上传文档的质量评分、类型等,对文档贡献者给予高额补贴、流量扶持。如果你也想贡献VIP文档。上传文档
查看更多
文献汇报;什么是文献汇报;为什么要进行文献汇报;怎样进行文献汇报;文献汇报的结构;如何选择文献;如何查找文献;如何查找文献;如何阅读文献;文献结构;选择文献;文献简介;文献背景(大背景和小背景);小背景(同行研究水平):Nevertheless, methods have emerged for bioconjugation with natural and unnatural amino acids in protein molecules6,7.Cysteine is a key residue for the chemical modification of proteins owing to the unique reactivity of the thiol functional group and the low abundance of cysteine residues in naturally occurring proteins8,9. Michael addition to maleimides and SN2 reaction with alkyl halides are commonly used for cysteine modification. The resulting conjugates tend to decompose in the presence of external bases or thiol nucleophiles10, which prompted the recent development of advanced cysteine bioconjugations for the improved stability of conjugates. The ability to achieve high levels of chemo- and regioselectivity through the judicious choice of metal and ligand design suggest that metal-mediated processes could be very attractive for the development of new bioconjugations. Existing metal-based transformations often rely on the use of functional handles12 or unnatural amino acids, such as 4-iodophenylalanine and aldehyde- or alkyne-containing amino acids3,4,13, and require high concentrations (mM) of derivatizing agents, which can cause off-target reactivity or purification problems. ;We considered that palladium complexes resulting from the oxidative addition of aryl halides or trifluoromethanesulfonates14 could be used for the transfer of aryl groups to cysteine residues in proteins (Fig. 1a). (For existing transition-metal-catalysed C–S bond-forming reactions, see ref. 15.) The efficiency and selectivity of the proposed reaction with the highly active palladium species may be hampered by the presence of a variety of functional groups within complex biomolecules. Furthermore, the presence of free thiols has been previously shown to inhibit palladium-catalysed cross-coupling reactions on peptides16, while Pd(II)-complexes have also been shown to exhibit prot

文档评论(0)

173****6081 + 关注
实名认证
文档贡献者

该用户很懒,什么也没介绍

1亿VIP精品文档

相关文档