Abstract
A variety of methods have been developed for assigning the aqueous domains of integral membrane proteins to either side of a biological membrane. Once the sequence of a protein is known from its DNA sequence it is possible to study the topology of the protein. This unit provides protocols in which the water-soluble domains can be tested for their accessibility to reagents added to membranes with a defined orientation. Tagging of hydrophilic regions of the protein with different epitopes and probing of their orientation with respect to the membrane is also described. Finally, a procedure for fusion of a reporter enzyme to truncated fragments of the protein is provided. The fusion protein is used as a sensor of sequence disposition relative to the membrane.
Original language | English (US) |
---|---|
Pages (from-to) | Unit 5.2 |
Journal | Current protocols in cell biology / editorial board, Juan S. Bonifacino ... [et al.] |
Volume | Chapter 5 |
State | Published - May 2001 |
All Science Journal Classification (ASJC) codes
- Cell Biology