Proteins-class {Pbase} | R Documentation

## The `Proteins` Class for Proteomics Data And Meta-Data

### Description

The `Proteins` class encapsulates data and meta-data for proteomics experiments. The class stores the protein sequences as well as specific subsets of interest, typically peptides, as ranges. The `Proteins` instances, the sequence and peptide slots are described by their respective metadata attributes.

### Objects from the Class

Objects can be created using its constructor `Proteins`. The constructor either takes a `fasta` file name as first argument, an `EnsDb` object or a named `uniprotIds` argument with valid UniProt accession numbers (not yet implemented).

The `Proteins` constructor with the `EnsDb` loads protein data directly from the `EnsDb` object. The additional arguments `filter`, `loadProteinDomains`, `columns` and `fetchLRG` allow to additionally specify if only proteins matching a certain criteria should be fetched, whether all protein domains should be added as `pranges`, optional additional annotation columns that should be retrieved and whether proteins from Locus Reference Genes (LRG) should also be retrieved from the database.

### Details

An instance of class `Proteins` is characterised by one or multiple protein sequences that can be accessed as `AAStringSet` with the `aa` accessor. Sequence-specific annotation, such as accession numbers, protein and gene names, ... is available with the `acols` method. General metadata such as the data of creation of the instance are stored as a `list` returned by the `metadata` accessor, which would typically contain a `created` character that documents when the object was created, a reference `genome` descriptor, a `UniProtRelease` with the release data of the UniProt database and possibly others.

Each sequence of a `Proteins` instance can also be characterised by a set of specific ranges describing peptides of interest. These peptide features can be extracted as an `AAStringSetList`, where each protein sequence contains 0 or more peptide features. These peptides features are encode as ranges along the original proteins sequences (a `list` of `IRanges`) that can be extracted with the `pranges` function. These peptide features have their own metadata describing for example peptide identification scores, number of missed cleavages, ... available with the `pcols` methods.

See also the `Pbase-data` vignette.

The `Proteins` constructor with argument `file` being an `EnsDb` object allows to retrieve protein sequences along with all their related protein domains from an `EnsDb` annotation database. The optional `filter` argument can be used to fetch only proteins matching the defined filtering criteria from the database. The `filter` argument takes an object extending the `AnnotationFilter` class, an `AnnotationFilterList` combining such objects or a filter expression in form of a `formula`. See the `AnnotationFilter` and `proteins` documentation for more details.

Additional annotation columns from the database that should be retrieved from the database and included into `acols` can be specified with the `columns` argument. The `listColumns` can be used to list all available annotation columns from the database. Ensembl protein IDs will be used as the `names` of the returned `Proteins` object. See the vignette from the `ensembldb` package for an overview of supported filters or below for some examples.

### Developement notes

Since version 0.2.0, `addIdentificationData` supports multiple identification file names to be added to a `Proteins` instance (argument renamed `filenames`) using either `mzID` or `mzR`. Added new `Pparams` parametrisation infrastructure.

See `news(package = "Pbase")` for a description of all changes.

Other possible metadata fields: `Uniprot.sw`, `biomaRt` instances.

### Slots

`metadata`:

  Object of class `"list"` containing global metadata, accessed with `metadata`.

`aa`:

  Object of class `"AAStringSet"` storing the protein sequences, accessed with `aa`.

`.__classVersion__`:

  Object of class `"Versions"` documenting the class verions. Intended for developer use and debugging.

### Extends

Class `"Versioned"`, directly.

### Methods

aa

  `signature(x = "Proteins")`: Returns an `AAStringSet` instance representing the sequences of the proteins.

pfeatures

  `signature(x = "Proteins")`: ...

pranges

  `signature(x = "Proteins")`: ...

metadata

  `signature(x = "Proteins")`: Returns a `list` of global metadata of the instance `x`, including data of instance creation or, if created from a set of UnitProt identifiers (see constructors above), the UniProt version and `UnitProt.WS` version number.

acols

  `signature(x = "Proteins")`: Returns a `DataFrame` of protein metadata.

pcols

  `signature(x = "Proteins")`: Returns a `list` of feature metadata.

avarLabels

  `signature(x = "Proteins")`: Returns the names of the sequences metadata.

pvarLabels

  `signature(x = "Proteins")`: Returns the names of the peptide feature metadata.

seqnames

  `signature(x = "Proteins")`: Returns the protein sequence names defined as UniProt accession numbers.

names

  `signature(x = "Proteins")`: Returns the protein sequence names defined as UniProt accession numbers. It is just a synonym for `seqnames`.

length

  `signature(x = "Proteins")`: Returns the number of proteins.

[

  `signature(x = "Proteins", i = "ANY", j = "missing")`: Creates a subset of the `Proteins` instance.

[[

  `signature(x = "Proteins", i = "ANY", j = "missing")`: Returns an `AAString` instance representing the sequence of the selected protein.

pfilter

  `signature(x = "Proteins", mass = "numeric", len = "numeric", ...)`: ...

cleave

  `signature(x = "Proteins", enzym = "character", missedCleavages = "numeric")`: Cleaves all proteins using the `enzym` rule while allowing `missedCleavages` missing cleavages. Please see `cleave` for details.

addIdentificationData

  `signature(object = "Proteins", id = "character", rmEmptyRanges = "logical", par = "Pparams")`: Adds identification data from an IdentMzMl file (`id`) to the Proteins `object`. If `rmEmptyRanges` is `TRUE` proteins without any identification data are removed. See `Pparams` for further settings.

addPeptideFragments

  `signature(object = "Proteins", filenames = "character", rmEmptyRanges = "logical", par = "Pparams")`: Adds identification data from a fasta file (`filenames`) to the Proteins `object`. Please note that both fasta files (the origin of the Proteins `object` and the ones given in `filenames`) must share the same Uniprot accession numbers. If `rmEmptyRanges` is `TRUE` proteins without any identification data are removed. See `Pparams` for further settings.

plot

  `signature(x = "Proteins", y = "missing")`: Plots all proteins and associated peptides using the `Gviz`/`Pviz` infrastructure.

show

  `signature(object = "Proteins")`: Displays object summary as text.

### Functions

rmEmptyRanges

  `signature(x = "Proteins")`

: removes proteins with empty peptide ranges.

proteotypic

  `signature(x = "Proteins")`: returns a modified Proteins object. `pcols(x)` gains a "Proteotypic" logical column, indicating of the peptide is proteotypic or now.

proteinCoverage

  `signature(pattern = "Proteins")`: calulates the coverage of proteins. `pcols(x)` gains a "Coverage" numeric column.

isCleaver

  `signature(x = "Proteins", missedCleavages = "numeric")`: Tests whether a Protein object was cleaved already.

### Author(s)

Laurent Gatto <lg390@cam.ac.uk>, Sebastian Gibb <mail@sebastiangibb.de> and Johannes Rainer <johannes.rainer@eurac.edu>

### References

Definition of the UniProt fasta comment format: http://www.uniprot.org/help/fasta-headers

### See Also

`calculateHeavyLabels`

### Examples

    ## Create a Protein object reading all proteins from a fasta file.
    fastaFiles <- list.files(system.file("extdata", package = "Pbase"),
                             pattern = "fasta", full.names = TRUE)
    p <- Proteins(fastaFiles)
    p
    metadata(p)

    ## Adding custom metadata
    metadata(p, "Comment") <- "I love R"
    metadata(p)

    ## Plotting
    plot(p[1:5], from = 1, to = 30)

    ## Cleaving
    pp <- cleave(p[1:100])
    pp <- proteotypic(pp)
    pp
    pcols(pp[1:2])

    plot(pp[1:2], from = 20, to = 30)

    ## Protein coverage
    pp <- proteinCoverage(pp)
    avarLabels(pp)
    acols(pp)$Coverage
    pp

    ## Add indentification data
    idfile <- system.file("extdata/Thermo_Hela_PRTC_selected.mzid",
                          package = "Pbase")
    p <- addIdentificationData(p, idfile)
    pranges(p)
    pfeatures(p)

    plot(p[1])
    plot(p[1], # the first protein has 36 peptides
         fill = c(rep("orange", 13), rep("steelblue", 13)))

    ## Retrieve a Proteins object from an EnsDb object: first load the annotation
    ## database for all human genes defined in Ensembl version 86.
    library(ensembldb)
    library(EnsDb.Hsapiens.v86)
    edb <- EnsDb.Hsapiens.v86

    ## Define a filter to retrieve all genes from chromosome Y
    sqnf <- SeqNameFilter("Y")
    ## Retrieve the proteins without protein domains but specify to retrieve in
    ## addition the transcript biotype for the encoding transcripts and the gene
    ## names
    prts <- Proteins(edb, filter = sqnf, loadProteinDomains = FALSE,
                     columns = c("tx_biotype", "gene_name"))
    aa(prts)
    acols(prts)

    ## The listColumns method lists all available columns from the database.
    listColumns(edb)

    ## Load all proteins from the gene ZBTB16 including all protein domains from
    ## the database. Here we pass the filter criteria as a formula to the method
    prts <- Proteins(edb, filter = ~ gene_name == "ZBTB16")

    ## List available pranges
    pcols(prts)

    ## Access the protein domains
    pcols(prts)$ProteinDomains

[Package Pbase version 0.22.1 Index]