Fusion protein linkers: Property, design and functionality

被引:1383
作者
Chen, Xiaoying [1 ]
Zaro, Jennica L. [1 ]
Shen, Wei-Chiang [1 ]
机构
[1] Univ So Calif, Sch Pharm, Dept Pharmacol & Pharmaceut Sci, Los Angeles, CA 90089 USA
关键词
Bifunctional recombinant proteins; Spacer; Pharmacokinetics; Pharmacodynamics; COLONY-STIMULATING FACTOR; HUMAN SERUM-ALBUMIN; CELL PENETRATING PEPTIDES; VIVO HALF-LIFE; IN-VIVO; MATRIX METALLOPROTEINASES; ESCHERICHIA-COLI; TRANSFERRIN RECEPTORS; CANCER-CELLS; LIGHT-CHAIN;
D O I
10.1016/j.addr.2012.09.039
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
As an indispensable component of recombinant fusion proteins, linkers have shown increasing importance in the construction of stable, bioactive fusion proteins. This review covers the current knowledge of fusion protein linkers and summarizes examples for their design and application. The general properties of linkers derived from naturally-occurring multi-domain proteins can be considered as the foundation in linker design. Empirical linkers designed by researchers are generally classified into 3 categories according to their structures: flexible linkers, rigid linkers, and in vivo cleavable linkers. Besides the basic role in linking the functional domains together (as in flexible and rigid linkers) or releasing the free functional domain in vivo (as in in vivo cleavable linkers), linkers may offer many other advantages for the production of fusion proteins, such as improving biological activity, increasing expression yield, and achieving desirable pharmacokinetic profiles. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:1357 / 1369
页数:13
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