A molecular machine rarely functions in isolation. ATP must be produced and supplied. Proteins must be encoded, translated, folded, transported, regulated, repaired, and eventually degraded. Cellular components communicate through networks of signals and interactions.
The result is organization at several levels. Individual proteins form complexes. Complexes participate in pathways. Pathways interact with other pathways. The cell must coordinate these activities while maintaining conditions compatible with life.
Research on protein machines, molecular chaperones, proteasomes, transport motors, and network biology shows extensive functional integration. The ribosome depends upon genetic information and energy. Protein-folding systems act on products of translation. Degradation machinery removes damaged or unneeded proteins. Transport systems move components to locations where they are required.
Integration does not automatically imply design. Natural selection can preserve interacting features when those interactions contribute to survival and reproduction. Existing systems can also be modified and incorporated into new relationships over time.
How did the dependencies among cellular subsystems arise, and how much of their historical development can be reconstructed from comparative and experimental evidence?
The design question becomes more significant when systems are considered together. Intelligent Design asks not merely where an individual component came from, but how information, machinery, energy, regulation, and quality control came to function as an integrated whole.