TY - JOUR
T1 - Molecular docking study on europium nanoparticles and mussel adhesive protein for effective detection of latent fingerprints
AU - Poorani, T. R.
AU - Ramya, C.
AU - Manohar, Ramya
N1 - Publisher Copyright:
© 2022 Informa UK Limited, trading as Taylor & Francis Group.
PY - 2023
Y1 - 2023
N2 - Background: Reflecting on the difficulty of finding the evidence of latent fingerprints on wet and rough surfaces, scientists need to visualise those fingermarks without any background interference and stable adhesion of visualising material over the fingermark residues. Objective: To stabilize the interaction with the fingermarks, the synthesized nanoparticles were conjugated with a highly adhesive biopolymer, Mussel Adhesive Protein (MAP) which can effectively interact with fingerprint deposits. Material and Methods: Rare earth metal, europium oxide and nanoparticles were used as a visualisation material to get high contrast and reduced background interference-based fingerprints. To stabilise the interaction with the fingermarks, the synthesised nanoparticles were conjugated with highly adhesive biopolymer, Mussel Adhesive Protein (MAP) which can effectively interacts with fingerprint deposits. A molecular docking study was done using Auto-Dock to find the binding affinity between the metal nanoparticle and the protein. Further, the stability of the bioconjugated with fingerprint residues was analysed by protein-protein interaction study through patch dock and PDB Sum. Results: The docking analysis between europium and nanoparticles with MAP was found to be −8.77 kcal/mol and −47.49 kcal/mol respectively. Protein-protein interaction studies showed a highest affinity for dermcidin and keratin with a binding affinity of −16.76 kcal/mol and −24.76 kcal/mol respectively. Conclusions: The docking studies showed an efficient interaction between the synthesised molecules and the fingermark residues. Results of these interaction studies proved that this bio-conjugated complex can be explored for efficient visualisation of low intensified fingermarks.
AB - Background: Reflecting on the difficulty of finding the evidence of latent fingerprints on wet and rough surfaces, scientists need to visualise those fingermarks without any background interference and stable adhesion of visualising material over the fingermark residues. Objective: To stabilize the interaction with the fingermarks, the synthesized nanoparticles were conjugated with a highly adhesive biopolymer, Mussel Adhesive Protein (MAP) which can effectively interact with fingerprint deposits. Material and Methods: Rare earth metal, europium oxide and nanoparticles were used as a visualisation material to get high contrast and reduced background interference-based fingerprints. To stabilise the interaction with the fingermarks, the synthesised nanoparticles were conjugated with highly adhesive biopolymer, Mussel Adhesive Protein (MAP) which can effectively interacts with fingerprint deposits. A molecular docking study was done using Auto-Dock to find the binding affinity between the metal nanoparticle and the protein. Further, the stability of the bioconjugated with fingerprint residues was analysed by protein-protein interaction study through patch dock and PDB Sum. Results: The docking analysis between europium and nanoparticles with MAP was found to be −8.77 kcal/mol and −47.49 kcal/mol respectively. Protein-protein interaction studies showed a highest affinity for dermcidin and keratin with a binding affinity of −16.76 kcal/mol and −24.76 kcal/mol respectively. Conclusions: The docking studies showed an efficient interaction between the synthesised molecules and the fingermark residues. Results of these interaction studies proved that this bio-conjugated complex can be explored for efficient visualisation of low intensified fingermarks.
UR - https://www.scopus.com/pages/publications/85142217848
UR - https://www.scopus.com/inward/citedby.url?scp=85142217848&partnerID=8YFLogxK
U2 - 10.1080/1354750X.2022.2145495
DO - 10.1080/1354750X.2022.2145495
M3 - Article
C2 - 36345920
AN - SCOPUS:85142217848
SN - 1354-750X
VL - 28
SP - 32
EP - 64
JO - Biomarkers
JF - Biomarkers
IS - 1
ER -