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PMID:15670776
Citation |
Lai, YP, Peng, YF, Zuo, Y, Li, J, Huang, J, Wang, LF and Wu, ZR (2005) Functional and structural characterization of recombinant dermcidin-1L, a human antimicrobial peptide. Biochem. Biophys. Res. Commun. 328:243-50 |
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Abstract |
Antimicrobial peptides from human skin are an important component of the innate immune response and play a key role as a first line of defense against infections. One such peptide is the recently discovered dermcidin-1L. To better understand its mechanism and to further investigate its antimicrobial spectrum, recombinant dermcidin-1L was expressed in Escherichia coli as a fusion protein and purified by affinity chromatography. The fusion protein was cleaved by factor Xa protease to produce recombinant dermcidin-1L. Antimicrobial and hemolytic assays demonstrated that dermcidin-1L displayed microbicidal activity against several opportunistic nosocomial pathogens, but no hemolytic activity against human erythrocytes even at concentrations up to 100 microM. Structural studies performed by circular dichroism spectroscopy indicated that the secondary structure of dermcidin-1L was very flexible, and both alpha-helix and beta-sheet structures might be required for the antimicrobial activity. Our results confirmed previous findings indicating that dermcidin-1L could have promising therapeutic potentials and shed new light on the structure-function relationship of dermcidin-1L. |
Links |
PubMed Online version:10.1016/j.bbrc.2004.12.143 |
Keywords |
Antimicrobial Cationic Peptides/chemistry; Antimicrobial Cationic Peptides/genetics; Antimicrobial Cationic Peptides/pharmacology; Bacteria/cytology; Bacteria/drug effects; Dose-Response Relationship, Drug; Escherichia coli/genetics; Escherichia coli/metabolism; Hemolysis/drug effects; Humans; Lethal Dose 50; Molecular Weight; Peptides/chemistry; Peptides/genetics; Peptides/pharmacology; Protein Conformation; Protein Structure, Secondary; Recombinant Proteins/chemistry; Recombinant Proteins/pharmacology; Structure-Activity Relationship |
Significance
Annotations
Gene product | Qualifier | GO Term | Evidence Code | with/from | Aspect | Extension | Notes | Status |
---|---|---|---|---|---|---|---|---|
GO:0042742: defense response to bacterium |
ECO:0000314: |
P |
The antimicrobial activity of DCD-1, in the form of purified rDCD-1L, was assessed using a microbicidal assay in vitro against five different microorganisms. rDCD-1L was show to be active against E. coli CMCC(B)44102, P. sputita, S. aureus CMCC(B)26003, and S. aureus293 with 50% of bacteria killed at the concentrations of 1.8, 0.5, 8.2, and 17.8 μg/mL, respectively (Figure 5). |
complete | ||||
GO:0051873: killing by host of symbiont cells |
ECO:0000314: |
P |
Human dermicidin, DCD-1, has the ability to kill cells of other organisms. The antimicrobial activity of DCD-1, in the form of purified rDCD-1L, was assessed using a microbicidal assay in vitro against five different microorganisms. rDCD-1L was show to be active against E. coli CMCC(B)44102, P. sputita, S. aureus CMCC(B)26003, and S. aureus293 with 50% of bacteria killed at the concentrations of 1.8, 0.5, 8.2, and 17.8 μg/mL, respectively (Figure 5). |
complete | ||||
GO:0002376: immune system process |
ECO:0000314: |
P |
Human dermicidin, DCD-1, plays a role in immune system processes. The antimicrobial immune system activity of DCD-1, in the form of purified rDCD-1L, was assessed using a microbicidal assay in vitro against five different microorganisms. rDCD-1L was show to be active against E. coli CMCC(B)44102, P. sputita, S. aureus CMCC(B)26003, and S. aureus293 with 50% of bacteria killed at the concentrations of 1.8, 0.5, 8.2, and 17.8 μg/mL, respectively (Figure 5). |
complete | ||||
GO:0016045: detection of bacterium |
ECO:0000314: |
P |
Human dermicidin, DCD-1, has the ability to detect bacterial cells and express antimicrobial activity against them. The antimicrobial activity of DCD-1, in the form of purified rDCD-1L, was assessed using a microbicidal assay in vitro against five different microorganisms. rDCD-1L was show to be active against E. coli CMCC(B)44102, P. sputita, S. aureus CMCC(B)26003, and S. aureus293 with 50% of bacteria killed at the concentrations of 1.8, 0.5, 8.2, and 17.8 μg/mL, respectively (Figure 5). |
complete | ||||
Notes
See also
References
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