Asset Details
MbrlCatalogueTitleDetail
Do you wish to reserve the book?
Exploring the Potential of Site-Selective Labeling on a Green Fluorescent Protein Through Lys–His Linchpin-Directed Modification
by
Bettati, Stefano
, Pioselli, Barbara
, Ronda, Luca
, Marchetti, Marialaura
, Raboni, Samanta
, Pianta, Elisa
, Campanini, Barbara
, Gritti, Alessandra
, Modafferi, Gloria
, Nardis, Ilaria De
, Bruno, Stefano
, Abbiati, Giorgio
, Faggiano, Serena
, Bova, Stefania
, Pirovano, Valentina
in
Biosensing Techniques - methods
/ green fluorescent protein (GFP)
/ Green Fluorescent Proteins - chemistry
/ Histidine - chemistry
/ Hydrogen-Ion Concentration
/ linchpin-directed modification (LDM)
/ Lysine - chemistry
/ Models, Molecular
/ protein biosensors
/ site-selective labeling
/ Staining and Labeling
2026
Hey, we have placed the reservation for you!
By the way, why not check out events that you can attend while you pick your title.
You are currently in the queue to collect this book. You will be notified once it is your turn to collect the book.
Oops! Something went wrong.
Looks like we were not able to place the reservation. Kindly try again later.
Are you sure you want to remove the book from the shelf?
Exploring the Potential of Site-Selective Labeling on a Green Fluorescent Protein Through Lys–His Linchpin-Directed Modification
by
Bettati, Stefano
, Pioselli, Barbara
, Ronda, Luca
, Marchetti, Marialaura
, Raboni, Samanta
, Pianta, Elisa
, Campanini, Barbara
, Gritti, Alessandra
, Modafferi, Gloria
, Nardis, Ilaria De
, Bruno, Stefano
, Abbiati, Giorgio
, Faggiano, Serena
, Bova, Stefania
, Pirovano, Valentina
in
Biosensing Techniques - methods
/ green fluorescent protein (GFP)
/ Green Fluorescent Proteins - chemistry
/ Histidine - chemistry
/ Hydrogen-Ion Concentration
/ linchpin-directed modification (LDM)
/ Lysine - chemistry
/ Models, Molecular
/ protein biosensors
/ site-selective labeling
/ Staining and Labeling
2026
Oops! Something went wrong.
While trying to remove the title from your shelf something went wrong :( Kindly try again later!
Do you wish to request the book?
Exploring the Potential of Site-Selective Labeling on a Green Fluorescent Protein Through Lys–His Linchpin-Directed Modification
by
Bettati, Stefano
, Pioselli, Barbara
, Ronda, Luca
, Marchetti, Marialaura
, Raboni, Samanta
, Pianta, Elisa
, Campanini, Barbara
, Gritti, Alessandra
, Modafferi, Gloria
, Nardis, Ilaria De
, Bruno, Stefano
, Abbiati, Giorgio
, Faggiano, Serena
, Bova, Stefania
, Pirovano, Valentina
in
Biosensing Techniques - methods
/ green fluorescent protein (GFP)
/ Green Fluorescent Proteins - chemistry
/ Histidine - chemistry
/ Hydrogen-Ion Concentration
/ linchpin-directed modification (LDM)
/ Lysine - chemistry
/ Models, Molecular
/ protein biosensors
/ site-selective labeling
/ Staining and Labeling
2026
Please be aware that the book you have requested cannot be checked out. If you would like to checkout this book, you can reserve another copy
We have requested the book for you!
Your request is successful and it will be processed during the Library working hours. Please check the status of your request in My Requests.
Oops! Something went wrong.
Looks like we were not able to place your request. Kindly try again later.
Exploring the Potential of Site-Selective Labeling on a Green Fluorescent Protein Through Lys–His Linchpin-Directed Modification
Journal Article
Exploring the Potential of Site-Selective Labeling on a Green Fluorescent Protein Through Lys–His Linchpin-Directed Modification
2026
Request Book From Autostore
and Choose the Collection Method
Overview
Protein-based biosensors require controlled and site-selective functionalization strategies to enable stable and oriented immobilization without compromising protein structure and signal transduction efficiency. We evaluated a chemoselective linchpin-directed modification (LDM) approach targeting Lys–His pairs as a tool for site-specific labeling of the model fluorescent biosensor green fluorescent protein (GFP). LDM molecules with variable spacer lengths were prepared, and a structure-guided computational workflow was implemented to map Lys–His distances on the protein and identify candidate modification sites. Experimental validation by UV-Vis spectroscopy and mass spectrometry demonstrated efficient conjugation and a final degree of labeling close to unity, consistent with single-site modification, with all LDM molecules selectively targeting the same histidine residue (His181), independently of spacer length. Structural analysis revealed that this residue is located within an accessible internal cavity that favors productive interactions with the reactive group. Importantly, the modification preserves GFP fluorescence and pH response, confirming retention of sensing functionality. These results demonstrate that LDM enables selective modification not only of surface residues, but also of structurally guided, non-surface residues. This approach provides the proof of concept of a new, promising strategy for the controlled functionalization and immobilization of protein-based biosensors.
Publisher
Multidisciplinary Digital Publishing Institute (MDPI),MDPI AG
This website uses cookies to ensure you get the best experience on our website.