How does a repressor find its operator in a sea of other sequences? It is not enough just for the regulatory protein to recognize the correct DNA.

How does a repressor find its operator in a sea of other sequences?

It is not enough just for the regulatory protein to recognize the correct DNA site.

The protein must also find it rapidly and bind to it sufficiently tightly to discriminate it from the millions of competing and overlapping nonspecific sites that are explored in the course of specific target localization.

One point to keep in mind while considering protein-DNA interactions is that such an interaction represents a dynamic equilibrium:Whether an operator has its (or a) particular repressor protein bound to it depends on:

1. the concentration of the regulatory protein in the cell,

2. the affinity between the repressor and the operator sequence and

3. the affinity between the repressor and other non-specific DNA binding sites.

Association constants: lac repressor + DNA to R-DNA complex

Repressor:lac operator 1-2 X 1013 M-1

other DNA 2-3 X 106 M-1

(specificity = KA(s)/KA(non-specific) = 107)

Repressor bound to inducerlac operator 2 X 1010 M-1--or some references suggest this is even lowerother DNA 2 X 106 M-1

When repressor is bound to allosteric regulator (allolactose in this case) non-specific binding competes more effectively with specific binding.

How a repressor recognizes and binds to an operator

The interaction between repressor and operator is often taken as a paradigm for sequence-specific DNA-protein interactions.

Each regulatory protein in E. coli must select its operator site (or sites) from among the five million or so base pairs of DNA in the cell.

For this organism, an operator (or any other cis acting site) must be at least 11-12 bases long in order to form a site that reoccurs at random less than once per genome.

Accordingly, regulatory proteins in E. coli bind tightly to specific DNA sequences that are about 15-20 base pairs long.

Operator Sequence and Structure:

A large number of operator sites have been identified and their DNA sequence has been determined.

One feature that is common to all operators is an imperfect two-fold axis of symmetry.

A perfectly symmetrical sequence is shown below.

>---- G C C A T G C G C A T G G C ----><---- C G G T A C G C G T A C C G ----<

Cap binding site:

Link to view structure

Lac repressor

lac operator: binding site for the lac repressor protein (lac I gene product)

Structure of Regulatory Proteins:Many DNA-binding regulatory proteins share features in common that reflect a common mode of DNA binding. Some of these features are:

(1) The active binding unit is a dimer of two identical globular polypeptide chains oriented oppositely in space to give a molecule with a two-fold axis of symmetry

phage lambda cI repressor proteinalpha helical region in contact with the major groove is in red.

(2) The critical contacts between the protein and the DNA are made by adjacent helices located at the binding face of each monomer. The helices are connected by a turn in the protein secondary structure. This helix-turn-helix motif is common to many regulatory proteins.

HTH

DNA structures

A, B and Z DNA differ with respect to diameter,

rise per base,number of base pairs per turn topology of the major and minor grooves

Cro

Why do the recognition helices contact the major groove?

What determines the specificity of interaction?

A=H bond acceptorD=H bonddonor

One of the most common DNA-protein interactions. Because of its specific geometry of H-bond acceptors, guanine can be unambiguously recognized by the side chain of arginine

Stereo view for phage lambda repressor

Specificity of protein-DNA interaction of due to:ability of amino acid side chains in the recognition helix to form hydrogen bonds with specific bases in its cis-acting site

multiple complementary interactions between the protein and the DNA that are dependent on the deformation of the helix and which increase the number of contact points

Main features of interactions between DNA and the helix-turn-helix motif of DNA binding proteins

Phage Lambda

Important Points: a handshake leads to a bear-hug

Specific recognition of DNA targets by the helix-turn-helix motif involves interactions between sides of the recognition helix and bases in the major groove of the DNA

But, specific recognition of DNA sequences is to a large extent governed by other interactions within complementary surfaces between the protein and the \

These interactions frequently involve H-bonds from protein main-chain atoms to the DNA backbone in both the major and the minor groove and are dependent on the sequence-specific deformability of the target DNA

DNA deformation induced by protein-binding.

The ease with which a stretch of DNA can be deformed can affect the affinity of protein binding to a specific sequence

CAP binding to its cis-acting site

cAMP binding domain in blue

red -- DNA phosphates whose ethylation interferes with cap binding

blue hypersenstivie to DNase I-- these phosphates bridge the cap-induced where the minor groove has been widened

Here the lac repressor tetramer is shown binding to two operators. Each dimer contacts one operator (either dark or light blue). The operators are 21 bases long.

MVA Fig. 26.33

Alberts Fig. 7-34

No direct H-bonding with bases!

All specific H-bonds occur via bridging water molecules!

Only direct contacts are H-bonds to the phosphate backbone!!!!

Yet mutations of these non-contact bases alter binding specificity

This suggests that the operator assumes a sequence-specific conformation that makes favorable contacts with therepressor known as

Indirect Readout

When tryptophan is added to crystals of aporepressor, the crystals shatter. When the tryptophan wedges itself into the protein, it changes the shape of the protein enough to break the lattices of the crystal

The orientation of the recognition helix shifts when tryptophan is bound.

trp repressor(HTH; allosteric)

trp repressor(HTH; allosteric)

His

Cys

?

?

Gal4

Gal4

p53DNA binding domain

major groove

minor groove

mutations that affectDNA binding are oncogenic

(beta sheet recognition element)

arc repressorfrom phage P22

arc repressorfrom P22

bZip

bZip homo- and heterodimers

max (bHLHzip)

max (bHLHzip)