Mirror image proteins

被引:48
|
作者
Zhao, Le [1 ]
Lu, Wuyuan [2 ,3 ,4 ,5 ]
机构
[1] Xi An Jiao Tong Univ, Sch Med, Affiliated Hosp 1, Xian, Peoples R China
[2] Xi An Jiao Tong Univ, Sch Life Sci & Technol, Minist Educ, Key Lab Biomed Informat Engn, Xian, Peoples R China
[3] Xi An Jiao Tong Univ, Frontier Inst Sci & Technol, Ctr Translat Med, Xian, Peoples R China
[4] Univ Maryland, Sch Med, Inst Human Virol, College Pk, MD USA
[5] Univ Maryland, Sch Med, Dept Biochem & Mol Biol, College Pk, MD USA
关键词
X-RAY-STRUCTURE; D-PEPTIDE INHIBITORS; TOTAL CHEMICAL-SYNTHESIS; D-AMINO ACIDS; LIPID-II; FUNGAL DEFENSIN; DRUG DISCOVERY; HIV-1; ENTRY; TARGET; CRYSTALLOGRAPHY;
D O I
10.1016/j.cbpa.2014.09.019
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Proteins composed entirely of unnatural D-amino acids and the achiral amino acid glycine are mirror image forms of their native L-protein counterparts. Recent advances in chemical protein synthesis afford unique and facile synthetic access to domain-sized mirror image D-proteins, enabling protein research to be conducted through 'the looking glass' and in a way previously unattainable, D-Proteins can facilitate structure determination of their native L-forms that are difficult to crystallize (racemic Xray crystallography); D-proteins can serve as the bait for library screening to ultimately yield pharmacologically superior D-peptide/D-protein therapeutics (mirror-image phage display); D-proteins can also be used as a powerful mechanistic tool for probing molecular events in biology. This review examines recent progress in the application of mirror image proteins to structural biology, drug discovery, and immunology.
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页码:56 / 61
页数:6
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