Adapter reagents for protein site specific dye labeling.

Biopolymers

Department of Chemistry, The Scripps Research Institute, 10550 N. Torrey Pines Rd., La Jolla, CA, 92037.

Published: May 2014

Chemoselective protein labeling remains a significant challenge in chemical biology. Although many selective labeling chemistries have been reported, the practicalities of matching the reaction with appropriately functionalized proteins and labeling reagents is often a challenge. For example, we encountered the challenge of site specifically labeling the cellular form of the murine Prion protein with a fluorescent dye. To facilitate this labeling, a protein was expressed with site specific p-acetylphenylalanine. However, the utility of this acetophenone reactive group is hampered by the severe lack of commercially available aminooxy fluorophores. Here we outline a general strategy for the efficient solid phase synthesis of adapter reagents capable of converting maleimido-labels into aminooxy or azide functional groups that can be further tuned for desired length or solubility properties. The utility of the adapter strategy is demonstrated in the context of fluorescent labeling of the murine Prion protein through an adapted aminooxy-Alexa dye.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4851436PMC
http://dx.doi.org/10.1002/bip.22481DOI Listing

Publication Analysis

Top Keywords

adapter reagents
8
site specific
8
murine prion
8
prion protein
8
labeling
7
protein
5
reagents protein
4
protein site
4
specific dye
4
dye labeling
4

Similar Publications

stilPCR increases the effective sequencing length of Illumina targeted next-generation sequencing.

PLoS One

December 2024

Division of Pulmonary and Critical Care Medicine, Zuckerberg San Francisco General Hospital and Trauma Centre, University of California, San Francisco, San Francisco, CA, United States of America.

Identifying pathogens, resistance-conferring mutations, and strain types through targeted amplicon sequencing is an important tool. However, due to the limitations of short read sequencing, many applications require the division of limited clinical samples. Here, we present stilPCR (single-tube Illumina long read PCR), which allows the generation of hemi-nested amplicons in a single tube, with Illumina indexes and adapters, effectively increasing the Illumina read length without increasing the input requirements of reagents or sample.

View Article and Find Full Text PDF

Background/aim: Precise molecular mechanisms underlying resistance to cisplatin-based chemotherapy remain unclear, while the activity of estrogen receptor-β (ERβ) has been suggested to be associated with chemosensitivity in urothelial cancer. We aimed to determine if GULP1, an adapter protein known to facilitate phagocytosis, could represent a downstream effector of ERβ and thereby modulate cisplatin sensitivity in bladder cancer.

Materials And Methods: GULP1 expression and cisplatin cytotoxicity were compared in bladder cancer lines.

View Article and Find Full Text PDF

Dual dye-labeled aptamers for detection of dichlorvos using ratiometric fluorescence resonance energy transfer.

Anal Chim Acta

November 2024

State Key Laboratory of Toxicology and Medical Countermeasures, Laboratory of Toxicant Analysis, Academy of Military Medical Sciences, Beijing, 100850, China. Electronic address:

Article Synopsis
  • Dichlorvos (DDVP) is a highly toxic pesticide, making the monitoring of its residues in the environment and human health crucial, but traditional detection methods are cumbersome and not suitable for on-site testing.
  • The study involved the development and testing of two aptamer probes, finding that DV55 was more effective than DV65 for detecting DDVP, with a fast reaction time of just 5 minutes and a detection range of 0-100 μM.
  • The research highlights the potential of these dual-labeled aptamer probes as a portable, efficient method for rapid on-site detection of DDVP, showing promising results for future applications in pesticide monitoring.
View Article and Find Full Text PDF

PAR-dCLIP: Enabling detection of RNA binding protein target transcripts bound at 5' termini through the incorporation of a decapping step.

Methods Enzymol

October 2024

Department of Biochemistry, Vanderbilt University School of Medicine, Nashville, TN, United States; Department of Pathology, Microbiology and Immunology, Vanderbilt University Medical Center, Nashville, TN, United States. Electronic address:

RNA binding proteins (RBPs) are responsible for facilitating a wealth of post-transcriptional gene regulatory functions. The role of an RBP on regulated transcripts can be investigated through a pull-down of the RBP and high-throughput sequencing (HTS) of the associated transcripts. Photoactivatable Ribonucleoside-Enhanced Crosslinking and Immunoprecipitation (PAR-CLIP), is one such pull-down method that isolates, detects, and sequences the cDNA of RBP-associated transcripts.

View Article and Find Full Text PDF

Src homology 3 (SH3) domains play a critical role in mediating protein-protein interactions (PPIs) involved in cell proliferation, migration, and the cytoskeleton. Despite their abundance in the human proteome, the functions and molecular interactions of many SH3 domains remain unknown, and this is in part due to the lack of SH3-domain-specific reagents available for their study. Affimer proteins have been developed as affinity reagents targeting a diverse range of targets, including those involved in PPIs.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!