Intramembrane proteases (IMPs) are localized within lipid bilayers of membranes-either the cell membrane or membranes of various organelles. Cleavage of substrates often results in release from the membrane, leading to a downstream biological effect. This mechanism allows different signaling events to happen through intramembrane proteolysis. Over the years, various mechanistically distinct families of IMPs have been discovered, but the research progress has generally been slower than for soluble proteases due to the challenges associated with membrane proteins. In this review we summarize how each mechanistic family of IMPs was discovered, which chemical tools are available for the study of IMPs, and which techniques have been developed fo...
Rhomboids were only discovered to be novel proteases in 2001, but progress on understanding this new...
Intramembrane proteases have the unusual property of cleaving peptide bonds within the lipid bilayer...
The serine proteases of the trypsin-like (S1) family play critical roles in many key biological proc...
Intramembrane proteases (IMPs) reside inside lipid bilayers and perform peptide hydrolysis in transm...
Proteases are considered attractive drug targets. Various drugs targeting classical, soluble proteas...
AbstractThe turn of the millennium coincided with the branding of a fundamentally different class of...
Proteases carry out a wide variety of physiological functions. This review presents a brief history ...
Intramembrane proteases are membrane enzymes whose active site is buried below the surface of the bi...
AbstractIntramembrane-cleaving proteases (I-CLiPs) are membrane embedded proteolytic enzymes. All su...
Regulated intramembrane proteolysis is an interesting process involved in a multitude of cellular pa...
AbstractIntramembrane-cleaving proteases are members of a novel type of enzyme that hydrolyse substr...
Matrix metalloproteinases (MMPs), originally discovered to function in the breakdown of extracellula...
The concept of proteases cleaving their substrates within the hydrophobic core of their transmembran...
Rhomboids are ubiquitous intramembrane serine proteases that cleave transmembrane substrates. Their ...
Proteins are responsible for carrying out most of the tasks in a living cell; transcription, transla...
Rhomboids were only discovered to be novel proteases in 2001, but progress on understanding this new...
Intramembrane proteases have the unusual property of cleaving peptide bonds within the lipid bilayer...
The serine proteases of the trypsin-like (S1) family play critical roles in many key biological proc...
Intramembrane proteases (IMPs) reside inside lipid bilayers and perform peptide hydrolysis in transm...
Proteases are considered attractive drug targets. Various drugs targeting classical, soluble proteas...
AbstractThe turn of the millennium coincided with the branding of a fundamentally different class of...
Proteases carry out a wide variety of physiological functions. This review presents a brief history ...
Intramembrane proteases are membrane enzymes whose active site is buried below the surface of the bi...
AbstractIntramembrane-cleaving proteases (I-CLiPs) are membrane embedded proteolytic enzymes. All su...
Regulated intramembrane proteolysis is an interesting process involved in a multitude of cellular pa...
AbstractIntramembrane-cleaving proteases are members of a novel type of enzyme that hydrolyse substr...
Matrix metalloproteinases (MMPs), originally discovered to function in the breakdown of extracellula...
The concept of proteases cleaving their substrates within the hydrophobic core of their transmembran...
Rhomboids are ubiquitous intramembrane serine proteases that cleave transmembrane substrates. Their ...
Proteins are responsible for carrying out most of the tasks in a living cell; transcription, transla...
Rhomboids were only discovered to be novel proteases in 2001, but progress on understanding this new...
Intramembrane proteases have the unusual property of cleaving peptide bonds within the lipid bilayer...
The serine proteases of the trypsin-like (S1) family play critical roles in many key biological proc...