Oxazolidinone-Mediated Sequence Determination of One-Bead One-Compound Cyclic Peptide Libraries

被引:19
|
作者
Elashal, Hader E. [1 ]
Cohen, Ryan D. [1 ,2 ]
Elashal, Heidi E. [1 ]
Raj, Monika [3 ]
机构
[1] Seton Hall Univ, Dept Chem, S Orange, NJ 07079 USA
[2] Merck & Co Inc, Dept Proc Res & Dev, Rahway, NJ 07065 USA
[3] Auburn Univ, Dept Chem & Biochem, Auburn, AL 36830 USA
关键词
COMBINATORIAL LIBRARIES; SPECTROMETRY; MEMBERS;
D O I
10.1021/acs.orglett.8b00717
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
A novel one-bead one-compound (OBOC) dualring-opening/cleavage approach for cyclic peptide sequencing was developed. The method selectively modifies serine, cysteine, threonine, and/or glutamic acid to an oxazolidinone-derived moiety, thereby increasing the susceptibility of the modified peptide backbone toward hydrolysis. The resulting linear peptide was then sequenced in 1 min by tandem mass spectrometry on a quadrupole time-of-flight instrument incorporating two-dimensional liquid chromatography and ion mobility spectrometry separation. To evaluate this approach, a library of cyclic peptides was successfully sequenced with 98% overall accuracy, demonstrating its robustness and broad substrate scope.
引用
收藏
页码:2374 / 2377
页数:4
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