Coding

Part:BBa_K4147009

Designed by: Ana Belem García González   Group: iGEM22_Tec-Chihuahua   (2022-10-08)
Revision as of 06:09, 10 October 2022 by Ana Belem (Talk | contribs)

(diff) ↠Older revision | Latest revision (diff) | Newer revision → (diff)


MsrA2 antimicrobial protein for purification with 6X-His tag

Antimicrobial protein from the arboreal tree frog Phyllomedusa bicolor, dermaseptin-b1 gene (AKA MsrA2) (BBa_K2577001) fused with a 6X-Hist tag for purification by metal affinity chromatography.

Usage and Biology

Dermaseptins (DRSs) are peptides produced by Hylid frogs, a group of É‘-helical shaped polycationic and short peptides (21-34 residues) containing a highly preserved tryptophan residue on N-terminal 3rd position, with hydrophobic residues and the polar cationic residues clusters in opposite sides [1]. The majority of the dermaseptin family peptides exhibit a wide variety of antibacterial activities. A broad range of microorganisms, including mollicutes, bacteria, fungi, protozoa, yeast, and enveloped viruses are all susceptible to the dermaseptins. Despite having a very similar sequence, the dermaseptins vary in how well they can neutralize different substances [2]. Dermaseptins also exhibit efficacy against various kinds of human cancer, making them anticancer peptides in addition to their antimicrobial capabilities.[1].

Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    COMPATIBLE WITH RFC[1000]


REFERENCES

[1] Bartels J. et al. Dermaseptins, Multifunctional Antimicrobial Peptides: A Review of Their Pharmacology, Effectivity, Mechanism of Action, and Possible Future Directions.

[2] Nicolas, P., & el Amri, C. (2009). The dermaseptin superfamily: A gene-based combinatorial library of antimicrobial peptides. Biochimica et Biophysica Acta (BBA) - Biomembranes, 1788(8), 1537–1550.

[edit]
Categories
Parameters
None