A new algorithm is reported to assist with the identification of protein interaction domains by comparing pairs of MALDI mass spectra recorded for protein digests treated with a binding partner versus an untreated control. Known as PRISM, for protein interactions from the spectra of masses, the algorithm imports m/z versus peak area data directly from a pair of MALDI mass spectra recorded for the control and reaction sample. The algorithm is shown to be able to successfully identify antigenic determinants for protein antigens within mixed protein digests. The algorithm has general utility for the comparative analysis of differences within any two mass spectra of any type and is easily implemented using a simple, intuitive graphical user int...
A set of new algorithms and software tools for automatic protein identification using peptide mass f...
Protein interaction in cells can be described at different levels. At a low interaction level, pro...
We describe an approach to screen large sets of MALDI-MS mass spectra for protein isoforms separated...
A new algorithm has been designed and tested to identify protein, or any other macromolecular, compl...
Prism (http://gordion.hpc.eng.ku.edu.tr/prism) is a website for protein interface analysis and predi...
PRISM is a web server for the querying, visualization and analysis of the protein interfaces and put...
Protein interaction in cells can be described at different levels. At a low interaction level, prote...
We have developed a new algorithm to identify proteins by means of peptide mass fingerprinting. Star...
The PRISM web server enables fast and accurate prediction of protein-protein interactions (PPIs). Th...
Protein interaction in cells can be described at different levels. At a low interaction level, prote...
The reliable identification of protein interaction partners and how such interactions change in resp...
The molecular scanner combines protein separation using gel electrophoresis with peptide mass finger...
Prediction of protein-protein interactions at the structural level on the proteome scale is importan...
We present a simple algorithm which allows accurate estimates of the similarity between peptide fing...
Protein identification is important in proteomics. Proteomic analyses based on mass spectra (MS) con...
A set of new algorithms and software tools for automatic protein identification using peptide mass f...
Protein interaction in cells can be described at different levels. At a low interaction level, pro...
We describe an approach to screen large sets of MALDI-MS mass spectra for protein isoforms separated...
A new algorithm has been designed and tested to identify protein, or any other macromolecular, compl...
Prism (http://gordion.hpc.eng.ku.edu.tr/prism) is a website for protein interface analysis and predi...
PRISM is a web server for the querying, visualization and analysis of the protein interfaces and put...
Protein interaction in cells can be described at different levels. At a low interaction level, prote...
We have developed a new algorithm to identify proteins by means of peptide mass fingerprinting. Star...
The PRISM web server enables fast and accurate prediction of protein-protein interactions (PPIs). Th...
Protein interaction in cells can be described at different levels. At a low interaction level, prote...
The reliable identification of protein interaction partners and how such interactions change in resp...
The molecular scanner combines protein separation using gel electrophoresis with peptide mass finger...
Prediction of protein-protein interactions at the structural level on the proteome scale is importan...
We present a simple algorithm which allows accurate estimates of the similarity between peptide fing...
Protein identification is important in proteomics. Proteomic analyses based on mass spectra (MS) con...
A set of new algorithms and software tools for automatic protein identification using peptide mass f...
Protein interaction in cells can be described at different levels. At a low interaction level, pro...
We describe an approach to screen large sets of MALDI-MS mass spectra for protein isoforms separated...