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Details of TopicalPdb ID 1126

PRIMARY INFORMATION
ID1126
PMID18670091
Year2008
SequenceMNFVMISIELSETMAL
IIVISGLLLCASSITT
TSSNDFYAVLHGNLSQ
SDRNELPKICGREFLT
DTLQSRSAGGVLVREN
EYPWVLLLTDPEWTRV
CTAVLISRRHVLTAAH
CVTNFPKDRKLEKDCH
YTTIQSTYLYVYPRTR
VNDALNIKRYTSSFSV
ARVMVHPSFSCSNATG
DIALLELTLNIFTEAS
PICMPHFNESIPKNAA
AAGFGKNPISNNTRPM
QVVNLTYQGTTGDRI
NameTrypsin
Length293
N-Terminal ModificationFree
C-Terminal ModificationFree
Linear/ CyclicLinear
ChiralityL
Chemical ModificationNone
Origin of PeptideBovine
Nature of Peptide/CargoEndogenous proteases trypsin is capable of digesting intercellular desmosomal proteins and hence used for in vitro epidermal separation and keratinocyte isolation
MechanismThe unique ability of proteases to cause selective epidermal separation has been in part explained by the proteolytic degradation of desmosomal proteins in the SC, which leads to cell dissociation
Cargo Sequence/StructureMALWTRLAPLLALLALWAPAPARAFVNQHLCGSHLVEALYLVCGERGFFYTPKARREVEGQVGALELAGGPGAGGLEGPPQKRGIVEQCCASVCSLYQLENYCN
Name of cargo
Bovine insulin
AssayPlasma glucose level (PGL) determination
EnhancerNone
Properties of enhancerNot applicable
Concentration200 µl of 2.5% trypsin (w/v)
Incubation time2 hour time interval upto 8 hours
Tissue permeability (value with units)Marked decrease in the PGL was observed in the group with trypsin pretreatment. The PGL was reduced to less than 60% of the initial value after 8 h in all groups with trypsin pretreatment
Tissue SampleBlood collected from the tail vein of diabetic rat
Ex vivo/In vivo/In vitroin vivo
SECONDARY INFORMATION
STRUCTURE
Predicted Structure
SMILESN.A.