化学
半胱氨酸
肽
组合化学
环肽
立体化学
化学合成
有机化学
生物化学
体外
酶
作者
Zhi’ang Chen,Yi Wee Lim,Jin Yong Neo,R. Chan,Li Quan Koh,Tsz Ying Yuen,Yee Hwee Lim,Charles W. Johannes,Zachary P. Gates
标识
DOI:10.1021/acs.analchem.3c01742
摘要
A "chemical linearization" approach was applied to synthetic peptide macrocycles to enable their de novo sequencing from mixtures using nanoliquid chromatography-tandem mass spectrometry (nLC-MS/MS). This approach─previously applied to individual macrocycles but not to mixtures─involves cleavage of the peptide backbone at a defined position to give a product capable of generating sequence-determining fragment ions. Here, we first established the compatibility of "chemical linearization" by Edman degradation with a prominent macrocycle scaffold based on
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