Dry lab

A dry lab is a laboratory where computational or applied mathematical analyses are done on a computer-generated model to simulate a phenomenon in the physical realm. Examples of such phenomena include a molecule changing quantum states, the event horizon of a black hole or anything that otherwise might be impossible or too dangerous to observe under normal laboratory conditions. This term may also refer to a lab that uses primarily electronic equipment, for example, a robotics lab. A dry lab can also refer to a laboratory space for the storage of dry materials. The term dry lab is also used in the photo printing industry to refer to photo printing systems that do not employ the use of "wet" photographic chemicals.

Dry labbing can also refer to supplying fictional (yet plausible) results in lieu of performing an assigned experiment.

As computing power has grown exponentially this approach to research, often referred to as in silico (as opposed to in vitro), has amassed more attention especially in the area of bioinformatics. More specifically, within bioinformatics, is the study of proteins or proteomics, which is the elucidation of their unknown structures and folding patterns. The general approach in the elucidation of protein structure has been to first purify a protein, crystallize it and then send X-rays through such a purified protein crystal to observe how these x-rays diffract into specific pattern—a process referred to as X-ray crystallography. However, many proteins, especially those embedded in cellular membranes, are nearly impossible to crystallize due to their hydrophobic nature. Although other techniques exists, such as ramachandran plotting and mass spectrometry, these alone generally do not lead to the full elucidation of protein structure or folding mechanisms.

As a means of surpassing the limitations of these techniques, projects such as Folding@home and Rosetta@home are aimed at resolving this problem using computational analysis, this means of resolving protein structure is referred to as protein structure prediction. Although many labs have a slightly different approach, the main concept is to find, from a myriad of protein conformations, which conformation has the lowest energy or, in the case of Folding@Home, to find relatively low energies of proteins that could cause the protein to misfold and aggregate other proteins to itself—like in the case of sickle cell anemia. The general scheme in these projects is that a small number of computations are parsed to, or sent to be calculated on, a computer, generally a home computer, and then that computer analyzes the likelihood that a specific protein will take a certain shape or conformation based on the amount of energy required for that protein to stay in that shape, this way of processing data is what is generally referred to as distributed computing. This analysis is done on an extraordinarily large number of different conformations, owing to the support of hundreds of thousands of home-based computers, in hopes to find the conformation of lowest possible energy or set of conformations of lowest possible energy relative to any conformations that are just slightly different. Although doing so is quite difficult, one can, by observing the energy distribution of a large number of conformations, despite the almost infinite number of different protein conformations possible for any given protein (see Levinthal Paradox), with a reasonably large number of protein energy samplings, predict relatively closely what conformation, within a range of conformations, has the expected lowest energy using methods in statistical inference. There are other factors such as salt concentration, pH, ambient temperature or chaperonins, which are proteins that assist in the folding process of other proteins, that can greatly affect how a protein folds. However, if the given protein is shown to fold on its own, especially in vitro, these findings can be further supported. Once we can see how a protein folds then we can see how it works as a catalyst, or in intracellular communication, e.g. neuroreceptor-neurotransmitter interaction. How certain compounds may be used to enhance or prevent the function of these proteins and how an elucidated protein overall plays a role in diseases such as Alzheimer's Disease or Huntington's Disease can also be much better understood.

...
Wikipedia