| Synonym | (Des-Gly77,Des-His78)-MBP (68-88 | 
                
                    | Species | Human | 
                
                    | Protein Accession | P02686 | 
                
                    | Purity | > 95% | 
                
                    | Endotoxin Level | < 1.0 EU per µg | 
                
                    | Biological Activity | N/A | 
                
                    | Expression System | E. coli | 
                
                    | Fusion Tag | None | 
                
                    | Predicted Molecular Mass | 2.5 kDa | 
                
                    | Formulation | Lyophilized | 
                
                    | Reconstitution | Reconstitute in sterile water to a concentration of 0.1-1.0 mg/ml. | 
                
                    | Storage & Stability | Store at -80°C. Avoid repeated freeze-thaw cycles. | 
            
            FAQ
            
                What is (Des-Gly77,Des-His78)-Myelin Basic Protein (68-8) and what is its significance in scientific
                research?
(Des-Gly77,Des-His78)-Myelin Basic Protein (68-8) is a modified peptide derived from a
                bovine species, and it plays a significant role in neurological studies, particularly in understanding
                diseases related to myelin sheath degradation. Myelin Basic Protein (MBP) is one of the major proteins
                in the myelin sheath, the protective covering that surrounds nerve fibers in the central nervous system.
                This protein is crucial for maintaining the structural integrity and function of myelin, and its
                breakdown is implicated in various demyelinating diseases, such as Multiple Sclerosis (MS).
The
                significance of studying this modified protein lies in its implications in understanding the
                pathophysiological mechanisms behind demyelination and neurodegeneration. Research on
                (Des-Gly77,Des-His78)-MBP (68-8) helps scientists explore how modifications in MBP contribute to myelin
                sheath stability and its susceptibility to damage. This particular peptide variant is characterized by
                the removal of the amino acids Glycine at position 77 and Histidine at position 78 from the MBP
                sequence, which alters its structure and potentially its interaction with other cellular components.
                
Understanding these interactions at a molecular level can provide critical insights into how MBP
                supports the myelin sheath and what happens when these processes fail. Moreover, this knowledge is
                essential for developing therapeutic strategies targeting MBP and its interactions. By elucidating how
                slight changes in the MBP sequence can impact myelin integrity, scientists are better equipped to
                identify targets for drug design and develop novel interventions that might slow or halt the progression
                of demyelinating diseases. Thus, (Des-Gly77,Des-His78)-MBP (68-8) remains an important focus of study in
                neurobiology and pharmaceutical research, helping bridge the gap between basic science and therapeutic
                application.
How does (Des-Gly77,Des-His78)-Myelin Basic Protein (68-8) contribute to
                understanding Multiple Sclerosis?
The contribution of (Des-Gly77,Des-His78)-Myelin Basic Protein
                (68-8) in understanding Multiple Sclerosis (MS) is pivotal due to its specific role in studying the
                mechanisms of myelin sheath degradation and repair. MS is an autoimmune disease characterized by the
                immune system attacking the central nervous system, leading to the deterioration of the myelin sheath,
                the protective coating of nerve fibers. This degradation interrupts nerve impulses, causing the wide
                array of neurological symptoms associated with MS.
Researchers investigate
                (Des-Gly77,Des-His78)-MBP (68-8) as part of their efforts to understand the exact biochemical triggers
                and pathological processes involved in MS. This peptide variant forms an essential component of studies
                focused on how immune responses target myelin proteins like MBP and how these responses lead to
                structural damage and functional impairment of neurons. The strategic focus on (Des-Gly77,Des-His78)-MBP
                is due to its modified structure, offering insights into how natural variations in the MBP sequence may
                influence its immunogenic properties and interaction with immune cells.
Understanding how
                (Des-Gly77,Des-His78)-MBP (68-8) is involved in MS involves looking at the role of T cells, which are
                central to mediating immune responses in the disease. Researchers aim to determine how modifications in
                MBP contribute to its recognition as a target by T cells, leading to autoimmunity. By studying this
                particular MBP variant, scientists can identify specific epitopes— the parts of an antigen to which an
                antibody attaches itself—that are targeted in MS, enhancing the understanding of autoimmune
                specificity.
Moreover, research on this peptide variant contributes to developing
                disease-modifying therapies by providing a platform for testing new compounds aimed at modifying T cell
                responses. These studies also aid in the design of biomarkers that might predict disease progression or
                response to treatment. In summary, the investigation into (Des-Gly77,Des-His78)-Myelin Basic Protein not
                only deepens understanding of the molecular underpinnings of MS but also drives innovation in
                therapeutic strategies and diagnostic tools aimed at better managing and potentially curing the
                disease.
What is the role of (Des-Gly77,Des-His78)-Myelin Basic Protein (68-8) in the development
                of therapeutic interventions?
(Des-Gly77,Des-His78)-Myelin Basic Protein (68-8) plays a critical
                role in the development of therapeutic interventions, particularly those targeting neurological
                disorders such as Multiple Sclerosis (MS). One of the significant challenges in treating MS and similar
                conditions is understanding the complex interactions between myelin proteins and the immune system,
                which contributes to disease pathology. Studying this modified protein is key to identifying specific
                targets for interventions and designing therapies that can alter disease progression.
Research
                leveraging (Des-Gly77,Des-His78)-MBP (68-8) primarily focuses on understanding how changes in protein
                structure affect immunogenicity—the ability to provoke an immune response. Since MS involves an
                autoimmune attack on myelin constituents like MBP, gaining insights into which MBP variants elicit
                immune responses can guide the development of immunomodulatory therapies. By identifying specific areas
                on MBP that are targeted by the immune system, researchers can develop treatments that either prevent
                the immune system from attacking these areas or enhance the body’s tolerance to these proteins, reducing
                inflammatory damage.
Furthermore, this peptide's role extends to drug discovery and testing. The
                availability of modified MBP peptides allows for high-throughput screening of compounds that can impact
                myelin integrity or modulate immune responses. (Des-Gly77,Des-His78)-MBP (68-8) serves as a model system
                for testing new drugs' efficacy and safety, providing an accelerated path for the development of novel
                pharmaceuticals.
Beyond drug development, (Des-Gly77,Des-His78)-MBP (68-8) is instrumental in
                vaccine research aimed at inducing tolerance to MBP components in autoimmune contexts. Vaccinology
                approaches using altered peptide ligands (APL) like this MBP variant can potentially retrain the immune
                system to be less reactive to myelin proteins. These strategies can pave the way for new MS therapy
                paradigms where immune tolerance is induced without broad immunosuppression, which is often associated
                with significant side effects.
In conclusion, the study of (Des-Gly77,Des-His78)-Myelin Basic
                Protein (68-8) supports the comprehensive approach required for effective therapeutic development. It
                does so by enabling precise targeting in drug design, aiding in the discovery of immune-regulatory
                mechanisms, and fueling the development of innovative therapeutic options to manage or even prevent
                demyelinating diseases.
Why is the study of (Des-Gly77,Des-His78)-Myelin Basic Protein (68-8)
                critical for unveiling the mechanisms of neurodegenerative diseases?
The study of
                (Des-Gly77,Des-His78)-Myelin Basic Protein (68-8) is vital for unveiling the mechanisms underlying
                neurodegenerative diseases due to its central role in understanding myelin integrity and immune
                interactions in the central nervous system (CNS). Neurodegenerative diseases, which include conditions
                such as Multiple Sclerosis (MS), Alzheimer's disease, and Parkinson's disease, often involve the
                breakdown or dysfunction of the protective myelin sheath covering nerve fibers. Therefore, MBP and its
                variants are key molecular players in the pathophysiology of these diseases.
One of the primary
                reasons for studying (Des-Gly77,Des-His78)-MBP (68-8) is to explore how structural alterations in myelin
                proteins affect their function and interaction with other cellular elements. This understanding helps
                elucidate the processes leading to myelin sheath degeneration. Myelin degradation leads to disrupted
                neuronal signaling, which is a hallmark in many neurodegenerative diseases. By studying specific MBP
                variants, researchers can determine how such modifications influence myelin's structural integrity and
                its effectiveness in insulating nerve fibers.
Additionally, the research on this MBP variant
                provides insights into autoimmune responses contributing to neurodegenerative disease progression.
                Diseases like MS which involve autoimmune destruction of myelin can serve as models to understand
                similar processes in other neurodegenerative conditions. The specificity of immune responses to
                particular myelin protein epitopes found in (Des-Gly77,Des-His78)-MBP offers clues on the mechanisms by
                which autoimmunity can lead to neurodegeneration. Identifying these specific immune targets and pathways
                is crucial for developing therapeutic strategies that mitigate immune-mediated damage without
                compromising the entire immune system.
Furthermore, the study of (Des-Gly77,Des-His78)-Myelin
                Basic Protein brings attention to potential biomarkers for early diagnosis and treatment monitoring. By
                focusing on molecular changes in MBP variants, researchers can identify early signals of disease onset
                or progression. These biomarkers could be critical for intervening in the disease processes at earlier
                stages, potentially slowing or preventing further neurodegeneration.
In summary,
                (Des-Gly77,Des-His78)-Myelin Basic Protein (68-8) serves as a critical research focus for advancing the
                understanding of neurodegenerative diseases. Its study bridges the knowledge gaps in myelin biology,
                immune interactions, and provides pathways for novel diagnostic and therapeutic approaches that are
                essential for better disease management and improved patient outcomes.
How does
                (Des-Gly77,Des-His78)-Myelin Basic Protein (68-8) facilitate advancements in biomarker
                discovery?
(Des-Gly77,Des-His78)-Myelin Basic Protein (68-8) facilitates advancements in
                biomarker discovery through its unique structural attributes, which provide critical insights into
                pathological processes associated with myelin degradation and neurological disorders. Biomarkers are
                essential tools in clinical practice and research as they assist in diagnosing diseases early,
                predicting disease progression, and evaluating therapeutic responses. Due to the intricate nature of
                neurodegenerative diseases and their multifactorial causes, identifying effective biomarkers is
                particularly challenging, making research in this area of great importance.
The value of
                (Des-Gly77,Des-His78)-MBP (68-8) in biomarker discovery lies in its ability to reflect specific
                pathological changes in the central nervous system. Alterations in MBP, such as this variant, could
                indicate changes in myelin integrity indicative of disease states like Multiple Sclerosis (MS). By
                providing a direct link to the components of myelin, this MBP variant serves as a candidate for
                detecting early signs of demyelination before significant clinical symptoms appear. 
Furthermore,
                studying this specific MBP variant enhances understanding of the immune processes that contribute to
                diseases, especially autoimmune conditions. Biomarkers derived from (Des-Gly77,Des-His78)-MBP offer
                insights into immune system alterations, helping predict the likelihood of a relapse in MS patients or
                the progression of other immune-mediated neurological diseases. By identifying the specific immune
                responses triggered by (Des-Gly77,Des-His78)-MBP variants, researchers can develop markers that help
                track how patients respond to specific therapies, potentially paving the way for personalized treatment
                approaches.
In addition, advanced techniques like mass spectrometry and immunoassays can be
                applied to study interactions and modifications in (Des-Gly77,Des-His78)-MBP, providing a platform for
                high-throughput biomarker screening. Researchers can use these techniques to identify proteins or
                peptides in biological fluids that are characteristic of disease states or treatment responses. This
                approach facilitates the identification of novel biomarkers that are not only relevant for diagnosis but
                also for monitoring disease activity and therapeutic efficacy.
Overall, the study of
                (Des-Gly77,Des-His78)-Myelin Basic Protein (68-8) is instrumental in advancing biomarker discovery. Its
                specific structure and modifications offer a window into the pathological processes affecting myelin and
                neuronal health, thereby aiding in the development of diagnostic and prognostic tools that are crucial
                in managing neurodegenerative and demyelinating diseases. Through continued research,
                (Des-Gly77,Des-His78)-MBP holds promise in transforming clinical practice by providing clinicians with
                the necessary tools to deliver timely and targeted interventions.