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2 Identity Matrix 3 Log-odds matrices 4 Current research |
In the process of evolution, from one generation to the next the amino acid sequences of an organism's proteins are gradually altered through the action of DNA mutations. For example, the sequence
Background
ALEIRYLRD
could mutate into the sequenceALEINYLRD
in one generation and possiblyAQEINYQRD
over a longer period of evolutionary time. Each amino acid is more or less likely to mutate into various other amino acids. For instance, a hydrophobic residue such as valine is more likely to stay hydrophobic than not, since replacing it with a hydrophilic residue could affect the folding and/or activity of the protein.
If we have two amino acid sequences before us, we should be able to say something about how likely they are to be derived from a common ancestor, or homologous. If we can line up the two sequences using a sequence alignment algorithm such that the mutations required to transform a hypothetical ancestor sequence into both of the current sequences would be evolutionarily plausible, then we'd like to assign a high score to the comparison of the sequences.
To this end, we will construct a 20x20 matrix where the th entry is equal to the probabiliy of the th amino acid being transformed into the th amino acid in a certain amount of evolutionary time. There are many different ways to construct such a matrix, called a substitution matrix. Here are the most commonly used ones:
The simplest possible substitution matrix would be one in which each amino acid is considered maximally similar to itself, but not able to transform into any other amino acid. This matrix would look like:
This matrix will succeed in the alignment of very similar amino acid sequences but will be miserable at aligning two distantly related sequences. We need to figure out all the probabilities in a more rigorous fashion. It turns out that an empirical examination of previously aligned sequences works best.
We express the probabilities of transformation in what are called log-odds scores. For our matrix M we define
where is the probability that amino acid transforms into amino acid and is the frequency of amino acid i. The base of the logarithm is not too important, and you will often see the same substitution matrix expressed in different bases.
What will our simple substitution matrix look like with log-odds scoring?
since there are 20 amino acids.
and
Hence, the matrix is:
One of the first amino acid substitution matrices, the PAM matrix was developed by Dayhoff in the 1970s. This matrix is calculated by observing the differences in closely related proteins. The PAM1 matrix measures the substitution rates when 1% of the amino acids have changed. The version that Dayhoff published was the PAM250 matrix. It's possible to go above PAM100 because if one residue changes five times, each change is counted.
A matrix for divergent sequences can be calculated from a matrix for closely related sequences by taking the second matrix to a power. For instance, we can roughly approximate the WIKI2 matrix from the WIKI1 matrix by saying where is WIKI1 and is WIKI2. This is how the PAM250 matrix is calculated.
Dayhoff's methodology of comparing closely related species turned out not to work very well for aligning evolutionarily divergent sequences. Sequence changes over long evolutionary time scales are not well approximated by compounding small changes that occur over short time scales. The BLOSUM series of matrices rectifies this problem. Henikoff and Henikoff constructed these matrices using multiple alignments of evolutionarily divergent proteins. The BLOSUM62 matrix includes only proteins that share at least 62% sequence identity, and so on. One would use a higher numbered BLOSUM matrix for aligning two closely related sequences and a lower number for more divergent sequences.
It turns out that the BLOSUM62 matrix does an excellent job detecting similarities in distant sequences, and this is the matrix used by default in most recent alignment applications like BLAST.
Current innovative approaches include incorporating secondary structure information into the sequences and substitution matrices. See this paper for an example of this direction of research.Identity Matrix
Log-odds matrices
PAM
BLOSUM
Current research