Designed by: Dingjian Zhang   Group: iGEM23_CPU-CHINA   (2023-09-11)

Auto cleaving linker B


With the advancement of molecular biology, numerous active proteins and peptides have been invented or discovered for therapeutic applications. Recombinant technology, renowned for its high expression levels and straightforward operations, has been widely employed in the biopharmaceutical sector. To achieve multi-target, multi-functional active proteins, it's imperative to link and fuse two or more proteins with known functions. This method of obtaining bifunctional or multifunctional fusion proteins has emerged as one of the novel approaches for new drug development and bioproduct research. Particularly, it has been extensively utilized in the preparation of bispecific single-chain antibodies (scFv) or antibody-drug conjugates [1-5].

Fusion proteins mainly consist of two components: the functional protein and the linker peptide. The functional protein refers to the original protein to be fused, which usually has a known structure and function, making its selection relatively straightforward. However, due to the significance of the linker peptide in the overall structure of the fusion protein, its selection and design demand careful research and consideration, ensuring the overall activity of the fusion protein remains unaltered [2]. Thus, studies on linker peptides have progressively come into focus.

What is it?

Below is the 3D structure of the EAAAK linker peptide, which is comprised of a simple α-helix. It is often used as a rigid linker peptide and is widely incorporated into fusion protein designs.

Modifying the binding action of antimicrobial peptides to bacterial cell membranes plays a pivotal role in regulating the antibacterial activity of the peptides. Yang et al. [6] replaced Glu16, Asp26, and Glu36 with Gln16, Asn26, and Gln36, respectively, increasing the electrostatic charge from +5.8 to +9.0. This modification heightened the positive charge level of LL‐37 without altering its spatial structure. Ga‐gnon et al. [7] found that peptide chain length also correlates with antimicrobial activity. Given the same peptide chain length, peptides with a longer length and more positive charge exhibited enhanced antibacterial effects.

Therefore, we anticipate that the linkers at both ends of the killing peptide shouldn't reduce its activity due to electrostatic interactions. To prevent negatively charged amino acids from approaching the killing peptide, we designed two types of linkers, positioning positively charged lysine around the killing peptide. This ensures that while designing fusion proteins, the killing activity remains potent.

As illustrated in the following figure, two lysine residues flank the red killing peptide. With the concentrated positive charge, the killing activity is intensified.

=What can it do?

BBa K4990005: EAAAK

Property:Rigid Linker

Rigid linker peptides are composed of amino acid residues that readily form stable secondary structures. In many instances, due to their capacity to form such stable secondary structures, flexible linker peptides can more effectively separate functional domains while maintaining their individual functionalities. The spatial separation of functional domains becomes crucial for the stability and bioactivity of fusion proteins when employing rigid linker peptides [8]. Research by George et al. [9] suggests that many natural rigid linker peptides adopt an α-helical structure. The most frequently used rigid α-helical linker peptide in recombinant fusion proteins is (EAAAK)n where n≤6. Owing to its internal hydrogen bonds and a compact backbone, the α-helix is rigid and stable. Experiments by Minsup et al. [10], using flexible (GGGGS) and rigid (EAAAK) linker peptides derived from White starflower beetle and beet armyworm antimicrobial proteins respectively, demonstrated that fusion proteins linked with rigid peptides showed significantly enhanced antibacterial activity compared to their parent proteins. In contrast, fusion proteins with flexible peptides did not exhibit this effect, suggesting that rigid linker peptides can effectively separate functional domains, resulting in proteins with activities surpassing those of the parent proteins. In another study, Guo et al. [11] employed flexible (GGGGS)n (n=1-3) and rigid (EAAAK)n (n=1-3) linker peptides to connect xylanase and mannanase. Comparatively, fusion enzymes linked with the rigid peptide exhibited superior thermal stability. Arai et al. [12] initially designed rigid linker peptide sequences A (EAAAK)n (n=2-5) based on empirical knowledge. This linker peptide adopts an α-helical conformation stabilized by salt bridges between the glutamate and lysine residues. Guo et al. [11] applied these linker peptides for the fusion of mannanase and xylanase, resulting in bi-functional enzyme activities. As the linker length increased, the catalytic efficiency of the fusion enzyme continuously improved. However, when repetitions reached four times, the catalytic efficiency started to decrease, suggesting that adjusting the repetition number of EAAAK can control the distance between structural domains.

In our designed fusion proteins, we extensively utilized this type of rigid self-hydrolyzing linker peptide. We constructed targeting peptides for cancer cell lysis, Fn-targeting peptides, and dual-targeting peptides. We hope that while maintaining the fusion protein's structural domain in an α-helical conformation, it possesses a self-hydrolyzing function, releasing the cytotoxic peptide portion, enabling it to exert its lethal effect.

How does it work?

Wu et al. [11] found that through their research on chitosan-fused rigid linker peptides, that rigid linker peptides exhibit self-cleaving properties under specific conditions. At pH=6-7, cleavage occurs. It's hypothesized that the EAAAK amino acid arrangement can form a stable hydrophilic α-helical structure. The forces at play can be attributed to the Glu-...Lys+ salt bridges between Glu and Lys. Hydrogen bonds are pivotal in forming these salt bridges, so pH greatly influences the stability of the salt bridges. At neutral pH, the strength of salt bridges is at its weakest, making cleavage more likely. Conversely, in high salt environments, the ionic strength can stabilize these bridges, preventing cleavage [12].


[1]Tao, L., Gao, M., & Zhou, H. (2015). Research progress on novel antibody-chemotherapy drug conjugates. Journal of Pharmaceutical Biotechnology, 22(3), 253-258.

[2] Gustavsson M,Lehtio J,Denman S,et al. Stable linker peptides for a cellulose-binding domain-lipase fusion protein expressed in pichia pastoris[J]. Protein Eng,2001,14(9):711-715.

[3] Wang SH,Zheng CJ,Liu Y,et al. Construction of multiform scFv antibodies using linker peptide[J]. J Genetics and Genomics,2008,35:313-316.

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[5] Shan D,Press OW,Tsu TT,et al. Characterization of scFv-Ig constructs generated from the Anti-CD20 mAb 1F5 using linker peptides of varying lengths[J].J Immunology,2014,162:6589-6595.

[6]Li, J., & Wang, C. (2015). Design of linker peptides and their application in fusion proteins. Journal of Food and Biotechnology, 1121-1127.

[7]Yang, Y., Ge, X., Liu, Y., et al. (2006). Fusion expression and antibacterial activity of modified human LL-37 antimicrobial peptide. Journal of the Fourth Military Medical University, 27(11), 1014-1017.

[8]Gagnon MC,Strandberg E,Grau ‐Campistany A,et al. Influenceof the length and charge on the activity of α‐helical amphipathicantimicrobial peptides[J]. Biochemistry,2017,56(11):1680-1695.

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[10]Lee M,Bang K,Kwon H,et al. Enhanced antibacterial activity of an attacin-coleoptericin hybrid protein fused with a helical linker[J]. Molecular Biology Reports,2013,40(6):3953-3960.

[11]Guo N,Zheng J,Wu L,et al. Engineered bifunctional enzymes of endo-1,4-β-xylanase/endo-1,4-β-mannanase were constructed for synergistically hydrolyzing hemicellulose[J]. Journal of Molecular Catalysis B:Enzymatic,2013,97:311-318.

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[13]Wu Y J, Fan C Y, Li Y K. Protein purification involving a unique auto-cleavage feature of a repeated EAAAK peptide[J]. Journal of Chromatography B, 2009, 877(31): 4015-4021.

[14]Marqusee S, Baldwin R L. Helix stabilization by Glu-... Lys+ salt bridges in short peptides of de novo design[J]. Proceedings of the National Academy of Sciences, 1987, 84(24): 8898-8902.

Sequence and Features

Assembly Compatibility:
  • 10
  • 12
  • 21
  • 23
  • 25
  • 1000