Stabilizing and destabilizing proteins

Data processing: measuring – calibrating – or testing – Measurement system in a specific environment – Biological or biochemical

Reexamination Certificate

Rate now

  [ 0.00 ] – not rated yet Voters 0   Comments 0

Details

C435S004000, C436S086000, C702S022000, C702S023000, C702S027000

Reexamination Certificate

active

06385546

ABSTRACT:

FIELD OF THE INVENTION
The present invention relates generally to the fields of protein chemistry, protein structural analysis and protein engineering.
BACKGROUND OF THE INVENTION
In a general way, the forces governing the conformational stability of globular proteins have, for the most part, been identified (Kauzmann, 1959; Dill, 1990; Honig and Yang, 1995. However, their relative and often their absolute roles remain elusive. The interactions that stabilize the folded, native structure sum to a free energy in the range of hundreds of kcal/mole (Kauzmann, 1959; Dill, 1990). Because the sum of the destabilizing forces is within the same range, the net stabilizing free energy is rather small, −5 to −20 kcal/mole (Makhatadze and Privalov, 1995).
SUMMARY OF THE INVENTION
Proteins are molecules that primarily consist of a polypeptide chain. Proteins can be modified in various ways known to those in the art, e.g., proteins can have carbohydrate sidechains or be derivatized to include modified amino acids.
As a group, proteins have a wide variety of functions and activities and can have more than one function or activity. Examples of protein functions and activities include acting as a ligand, a binding receptor, a co-factor, a regulator of gene expression, a fluorophore, a chromophore, an ion pump, a transducer of energy from one form to another, a light energy harvester, and as catalyst in many types of transformations of another molecule, called a substrate, or even themselves. We make no effort to distinguish between a function or an activity, and thus use the terms interchangeably or together.
The subset of proteins that are catalytic proteins are referred to in the art, and herein, as enzymes. These are often the most commercially important proteins and function in processes that produce a product from a substrate in part or wholly through the action of one or more enzymes.
As used herein, the term protein is used to refer to all manner of polypeptide based molecules independent of their additional features or their natural or commercial functions. The term enzyme is reserved for that set of proteins that are catalytically active in the transformation of a substrate molecule or themselves.
When specifically referring to the proteins used in and produced by the methods of this invention particular terms are used in this specification. The terms known protein or native protein are used to describe a protein having an amino acid sequence that will be altered in a method of this invention. A known protein is a protein known to one conducting a method of this invention. A known protein can be a wild-type protein, which is a protein the amino acid sequence of which has not been altered from that found in nature. The term known enzyme is used analogously to the use of known protein. These terms are not used herein to mean that the protein used as the starting material must have an amino acid sequence which was never changed from one that is found in nature, although that will frequently be the case. The amino acid sequence of the starting protein can have been previously altered in a variety of ways. The starting protein will often be a protein the sequence of which was previously altered in a method of this invention. Previously altered proteins are considered known proteins for purposes of this specification.
The term mutant protein is used herein to refer to a protein produced through the application of a method of this invention to a known protein. However, in some context mutant protein is also used to describe a protein reported in the literature. In such cases the use will be understood in context.
We use the term stability to refer to the ability of a protein to resist the effects of various conditions that can cause the protein to denature, i.e. to unfold partly or fully, or to become functionally impaired, non-functional, partially active or inactive. Many conditions can cause proteins to denature or can negatively impact the function or activity of a protein including heat (temperatures above the temperature optimum of the known protein), cold (temperature below the temperature optimum of the known protein), organic and inorganic solvents, co-solvents, co-solutes and pH. Solvents include non-water based liquids, e.g., ethanol. Co-solvents include mixtures of various proportions of solvents and water, e.g, a mixture of ethanol and water. Co-solutes are other molecules in solution along with the protein. Co-solutes can include ions, e.g., Na
+
, organic and inorganic compounds and their salts, e.g. detergents, urea and Guanidine hydrochloride.
In the simplest case, a mutant protein created by a method according to this invention is considered more stable when compared to the known protein if the mutant protein functions or has activity under conditions where the known protein does not function or is inactive. However, many improvements seen in a mutant protein will be in degree rather than in kind. Therefore, it is also said that a mutant protein created by the application of methods of this invention is more stable when compared to the known protein if the mutant protein can function to a greater extent or have greater activity in the presence of a greater degree of a given condition than the known protein. For example, if the mutant protein functions or has greater activity than the known protein (1) at a given temperature, (2) in the presence of co-solvents or co-solutes or (3) under other conditions that negatively impact the function or activity of the known protein, then the mutant protein is said to be more stable when compared to the known protein.
The term flexibility is used to refer to the freedom of a protein to assume differing conformations. Often, the conformations that a protein can assume are not very different, but this is not always the case as large changes can occur on binding to other molecules.
As used herein, the terms “solvent accessible surface area” or “accessible surface area” are used when referring to atoms exposed on the surface of a protein in native or extended conformation. Solvent accessible surface area and accessible surface area are the locus of points mapped out in two dimensions when a probe, usually 1.4 angstroms in radius, is rolled, computationally, across the van der Waals surface of the molecule. It is thus larger than the van der Waals chemical radius of the molecule, and many parts of the van der Waals surface can not be contacted by a probe of finite size, as described in Lee and Richards (1971). These terms may be abbreviated to “surface area” or even “area” but these terms are also used to refer to the surface area of atoms generally, i.e., the area of a buried atom is zero. In such cases one will understand the meaning from the context.
It is well established that amino acids are buried to various extents in various places in protein structures.
It is well established that amino acids are buried to various extents in various places in protein structures. This variety can be taken advantage of to tailor the effect of altering, by more or less, the amount of buried charged surface in a protein to achieve a desired result. For ease in discussing the range of burial of amino acids, particular terms are used herein to describe the degree of burial of amino acid residues in the native, or folded, conformation of a protein. Fully buried amino acids are those that are approximately 90% or more buried in the native conformation. Partially buried amino acids are those that are not fully exposed or fully buried. For ease of conceptualization, we often use partially buried to refer to amino acids that are between approximately 10% to approximately 90% buried in the native conformation. Amino acids that are substantially inaccessible to solvents are amino acids that are at least about 50% buried in the native conformation of a known protein as seen in the analysis taught herein.
In this specification we refer to amino acids that are outside of and not interacting with an active site or binding site of a protein. In usin

LandOfFree

Say what you really think

Search LandOfFree.com for the USA inventors and patents. Rate them and share your experience with other people.

Rating

Stabilizing and destabilizing proteins does not yet have a rating. At this time, there are no reviews or comments for this patent.

If you have personal experience with Stabilizing and destabilizing proteins, we encourage you to share that experience with our LandOfFree.com community. Your opinion is very important and Stabilizing and destabilizing proteins will most certainly appreciate the feedback.

Rate now

     

Profile ID: LFUS-PAI-O-2829378

  Search
All data on this website is collected from public sources. Our data reflects the most accurate information available at the time of publication.