Talin protein

Talin, middle domain
Identifiers
Symbol	Talin_middle
Pfam	PF09141
InterPro	IPR015224
SCOP	1sj7
SUPERFAMILY	1sj7
Available protein structures: Pfam structures PDB RCSB PDB; PDBe; PDBj PDBsum structure summary

talin 1
Identifiers
Symbol	TLN1
Alt. symbols	TLN
Entrez	7094
HUGO	11845
OMIM	186745
RefSeq	NM_006289
UniProt	Q9Y490
Other data
Locus	Chr. 9 p23-p21

talin 2
Identifiers
Symbol	TLN2
Entrez	83660
HUGO	15447
OMIM	607349
RefSeq	NM_015059
UniProt	Q9Y4G6
Other data
Locus	Chr. 15 q15-q21

Talin is a high-molecular-weight cytoskeletal protein concentrated at regions of cell–substratum contact and, in lymphocytes, at cell–cell contacts. Discovered in 1983 by Keith Burridge and colleagues, talin is a ubiquitous cytosolic protein that is found in high concentrations in focal adhesions. It is capable of linking integrins to the actin cytoskeleton either directly or indirectly by interacting with vinculin and alpha-actinin.

Integrin receptors are involved in the attachment of adherent cells to the extracellular matrix and of lymphocytes to other cells. In these situations, talin codistributes with concentrations of integrins in the plasma membrane. Furthermore, in vitro binding studies suggest that integrins bind to talin, although with low affinity. Talin also binds with high affinity to vinculin, another cytoskeletal protein concentrated at points of cell adhesion. Finally, talin is a substrate for the calcium-ion activated protease, calpain II, which is also concentrated at points of cell–substratum contact.

Protein domains

Talin consists of a large C-terminal rod domain that contains bundles of alpha helices and an N-terminal FERM (band 4.1, ezrin, radixin, and moesin) domain with three subdomains: F1, F2, and F3. The F3 subdomain of the FERM domain contains the highest affinity integrin-binding site for integrin β tails and is sufficient to activate integrins.

Middle domain

Structure

Talin also has a middle domain, which has a structure consisting of five alpha helices that fold into a bundle. It contains a vinculin binding site (VBS) composed of a hydrophobic surface spanning five turns of helix four.

Function

Activation of the VBS leads to the recruitment of vinculin to form a complex with the integrins which aids stable cell adhesion. Formation of the complex between VBS and vinculin requires prior unfolding of this middle domain: once released from the talin hydrophobic core, the VBS helix is then available to induce the 'bundle conversion' conformational change within the vinculin head domain thereby displacing the intramolecular interaction with the vinculin tail, allowing vinculin to bind actin.

Talin carries mechanical force (of 7-10 piconewton) during cell adhesion. It also allows cells to measure extracellular rigidity, since cells in which talin is prevented from forming mechanical linkages can no longer distinguish whether they are on a soft or rigid surface.

Vinculin binding site

VBS
human vinculin head (1-258) in complex with talin's vinculin binding site 3 (residues 1944-1969)
Identifiers
Symbol	VBS
Pfam	PF08913
InterPro	IPR015009
Available protein structures: Pfam structures PDB RCSB PDB; PDBe; PDBj PDBsum structure summary

Function

Vinculin binding sites are protein domains predominantly found in talin and talin-like molecules, enabling binding of vinculin to talin, stabilising integrin-mediated cell-matrix junctions. Talin, in turn, links integrins to the actin cytoskeleton.

Structure

The consensus sequence for vinculin binding sites is LxxAAxxVAxxVxxLIxxA, with a secondary structure prediction of four amphipathic helices. The hydrophobic residues that define the VBS are themselves 'masked' and are buried in the core of a series of helical bundles that make up the talin rod.

Activation of the integrin αIIbβ3

File:T INT 054.jpg

Model of talin-induced integrin activation

A structure–function analysis reported recently provides a cogent structural model (see top right) to explain talin-dependent integrin activation in three steps:

1. The talin F3 domain (surface representation; colored by charge), freed from its autoinhibitory interactions in the full-length protein, becomes available for binding to the integrin.
2. F3 engages the membrane-distal part of the β3-integrin tail (in red), which becomes ordered, but the α–β integrin interactions that hold the integrin in the low-affinity conformation remain intact.
3. In a subsequent step, F3 engages the membrane-proximal portion of the β3 tail while maintaining its membrane–distal interactions.

Human proteins containing this domain

TLN1; TLN2;

See also

• Actin-binding protein
• Merlin (protein) an acronym for "Moesin-Ezrin-Radixin-Like Protein"

External links

• MBInfo: Talin
• MBInfo: Talin activates Integrin
• Talin-1 UniProtKB/Swiss-Prot entry Q9Y490
• Talin substrate for calpain – PMAP The Proteolysis Map animation.
• Talin-1 Info with links in the Cell Migration Gateway
• Talin-2 Info with links in the Cell Migration Gateway
• Integrins at the US National Library of Medicine Medical Subject Headings (MeSH)