机构:
Boston Univ, Dept Chem, 590 Commonwealth Ave, Boston, MA 02215 USA
Boston Univ, Sch Med, Program Biomol Pharmacol, Boston, MA 02118 USABoston Univ, Dept Chem, 590 Commonwealth Ave, Boston, MA 02215 USA
Allen, Karen N.
[1
,2
]
Entova, Sonya
论文数: 0引用数: 0
h-index: 0
机构:
MIT, Dept Biol, 77 Massachusetts Ave, Cambridge, MA 02139 USABoston Univ, Dept Chem, 590 Commonwealth Ave, Boston, MA 02215 USA
Entova, Sonya
[3
]
Ray, Leah C.
论文数: 0引用数: 0
h-index: 0
机构:
Boston Univ, Sch Med, Program Biomol Pharmacol, Boston, MA 02118 USABoston Univ, Dept Chem, 590 Commonwealth Ave, Boston, MA 02215 USA
Ray, Leah C.
[2
]
Imperiali, Barbara
论文数: 0引用数: 0
h-index: 0
机构:
MIT, Dept Biol, 77 Massachusetts Ave, Cambridge, MA 02139 USA
MIT, Dept Chem, Cambridge, MA 02139 USABoston Univ, Dept Chem, 590 Commonwealth Ave, Boston, MA 02215 USA
Imperiali, Barbara
[3
,4
]
机构:
[1] Boston Univ, Dept Chem, 590 Commonwealth Ave, Boston, MA 02215 USA
[2] Boston Univ, Sch Med, Program Biomol Pharmacol, Boston, MA 02118 USA
[3] MIT, Dept Biol, 77 Massachusetts Ave, Cambridge, MA 02139 USA
Monotopic membrane proteins, classified by topology, are proteins that embed into a single face of the membrane. These proteins are generally underrepresented in the Protein Data Bank (PDB), but the past decade of research has revealed new examples that allow the description of generalizable features. This Opinion article summarizes shared characteristics including oligomerization states, modes of membrane association, mechanisms of interaction with hydrophobic or amphiphilic substrates, and homology to soluble folds. We also discuss how associations of monotopic enzymes in pathways can be used to promote substrate specificity and product composition. These examples highlight the challenges in structure determination specific to this class of proteins, but also the promise of new understanding from future study of these proteins that reside at the interface.