This paper presents rapid protein purification and proteolysis methods that integrate membrane technology and pipet tips. Pushing a protein-containing solution through a protease-modified membrane at the end of a pipet tip digests proteins in 30 s or less, and the short proteolysis time avoids reformation of disulfide bonds to enable tryptic digestion without alkylation of cysteine residues. Moreover, proteolysis is more complete than digestion for 30 min in solution. Antibody digestion at the end of a pipet tip leads to 100% peptide coverage in MS analyses. Similarly, when membranes contain Ni<sup>2+</sup> complexes, pipetting aqueous polyhistidine-tagged protein through the membrane and subsequent rinsing and elution yield purified polyhi...
In bottom-up proteomics, rapid and efficient protein digestion is crucial for data reliability. Howe...
Despite recent developments in bottom‐up proteomics, the need still exists in a fast, uncomplicated,...
The importance of membrane proteins in biological systems is indisputable; however, their amphipathi...
Functionalized porous membranes are powerful tools for rapid protein isolation or digestion prior to...
Sequential adsorption of poly(styrene sulfonate) (PSS) and proteases in porous nylon yields enzymat...
In proteomics, detergents and chaotropes are indispensable for proteome analysis, not only for prote...
The human proteome project will demand faster, easier, and more reliable methods to isolate and puri...
Analytical advantages of using multiple enzymes for sample digestion (MED), primarily an increase of...
Several proteomics approaches are available that are defined by the level (protein or peptide) at wh...
Conventional sample preparation protocols for phosphoproteome analysis require multiple time-consumi...
Conventional sample preparation protocols for phosphoproteome analysis require multiple time-consumi...
Overproduction and purification of membrane proteins are generally challenging and time-consuming pr...
A method for the rapid proteolytic digestion of low picomole to low femtomole amounts of proteins in...
Membrane proteins are fairly refractory to digestion especially by trypsin. Less specific proteases ...
Membrane proteins constitute around 20–30 % of the proteins encoded by mammalian genes, are involved...
In bottom-up proteomics, rapid and efficient protein digestion is crucial for data reliability. Howe...
Despite recent developments in bottom‐up proteomics, the need still exists in a fast, uncomplicated,...
The importance of membrane proteins in biological systems is indisputable; however, their amphipathi...
Functionalized porous membranes are powerful tools for rapid protein isolation or digestion prior to...
Sequential adsorption of poly(styrene sulfonate) (PSS) and proteases in porous nylon yields enzymat...
In proteomics, detergents and chaotropes are indispensable for proteome analysis, not only for prote...
The human proteome project will demand faster, easier, and more reliable methods to isolate and puri...
Analytical advantages of using multiple enzymes for sample digestion (MED), primarily an increase of...
Several proteomics approaches are available that are defined by the level (protein or peptide) at wh...
Conventional sample preparation protocols for phosphoproteome analysis require multiple time-consumi...
Conventional sample preparation protocols for phosphoproteome analysis require multiple time-consumi...
Overproduction and purification of membrane proteins are generally challenging and time-consuming pr...
A method for the rapid proteolytic digestion of low picomole to low femtomole amounts of proteins in...
Membrane proteins are fairly refractory to digestion especially by trypsin. Less specific proteases ...
Membrane proteins constitute around 20–30 % of the proteins encoded by mammalian genes, are involved...
In bottom-up proteomics, rapid and efficient protein digestion is crucial for data reliability. Howe...
Despite recent developments in bottom‐up proteomics, the need still exists in a fast, uncomplicated,...
The importance of membrane proteins in biological systems is indisputable; however, their amphipathi...