Salt-sensitive intein for large-scale polypeptide production

被引:1
作者
Lee, Yi-Zong [1 ,2 ]
Sue, Shih-Che [2 ,3 ]
机构
[1] Natl Tsing Hua Univ, Instrument Ctr, Hsinchu, Taiwan
[2] Natl Tsing Hua Univ, Inst Bioinformat & Struct Biol, Hsinchu, Taiwan
[3] Natl Tsing Hua Univ, Dept Life Sci, Hsinchu, Taiwan
来源
CHEMICAL AND SYNTHETIC BIOLOGY APPROACHES TO UNDERSTAND CELLULAR FUNCTIONS - PT A | 2019年 / 621卷
关键词
NPU DNAE INTEIN; RECOMBINANT PROTEINS; CXCL4; CHEMOKINES; PURIFICATION;
D O I
10.1016/bs.mie.2019.02.024
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
In this chapter, we propose to use salt-sensitive intein as a fusion protein to promote polypeptide expression; the removal of intein from the target sequence requires no enzyme, only a buffer change. The method will be particularly helpful for large-scale polypeptide preparations. Intein is an enzyme that can perform N- and C-terminal self-cleavage. Upon introduction of a mutation to eliminate the N-terminal cleavage activity, the C-terminal cleavage function can still be preserved. This feature was used to develop intein as a fusion protein through conjugation with a given sequence to promote protein expression in a biosynthesis system. Fused intein could later be separated from the target sequence through a C-terminal self-cleavage reaction. Here, a type of salt-sensitive intein is characterized in which ionic strength becomes an effector to control the self-cleavage activity. Low salt concentrations favor the cleavage reaction. Thus, using salt-sensitive intein as a fusion protein simply requires a buffer change to activate the self-cleavage mechanism, which makes it an enzyme-free process. This process has many advantages, including low cost, no extra residue remaining after cleavage, feasibility for preparing proteins starting from a non-Met codon and a special benefit for producing isotope-labeled peptides.
引用
收藏
页码:111 / 130
页数:20
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