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Overview of HLA-DRB1 and Its Role in the Immune System | LifeTein Peptide Blog

Allele DRB1*01:01 Allele DRB1*03:01 Allele DRB1*04:01 Allele DRB1*04:02 Allele DRB1*04:04 Allele DRB1*04:05 Allele DRB1*05:01 Allele DRB1*07:01 Allele DRB1*11:01 Allele DRB1*13:01 Allele DRB1*15:01 Allele DRB1*15:02 HLA-DRB1 Gene and Protein Function HLA-DRB1

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HLA-DRB1 Gene and Protein Function

HLA-DRB1 is part of the HLA class II beta chain paralogs. The class II molecule is a heterodimer composed of an alpha (DRA) and a beta chain (DRB), both of which are anchored in the membrane. This molecule is crucial in the immune system as it presents peptides from extracellular proteins. Class II molecules are expressed on antigen-presenting cells. The beta chain, approximately 26-28 kDa, is encoded by six exons. Exon one encodes the leader peptide; exons two and three encode the two extracellular domains; exon four encodes the transmembrane domain; and exon five encodes the cytoplasmic tail. The beta chain contains all polymorphisms that determine peptide binding specificities. Hundreds of DRB1 alleles exist, some of which are associated with certain diseases. For instance, DRB1*1302 is associated with the persistence of acute and chronic hepatitis B virus infection. Additionally, this gene has multiple pseudogenes.

Gene and Protein Complex Functionality

HLA-DRB1 facilitates several functions, including MHC class II receptor activity, peptide antigen binding, and signaling receptor binding. It is involved in processes such as the positive regulation of immune response, gene expression regulation, and leukocyte differentiation. This gene’s products are located in the bounding membrane of organelles, on the external side of the plasma membrane, and within the immunological synapse. HLA-DRB1 is part of the MHC class II protein complex and is implicated in various diseases, including asthma, autoimmune diseases, bacterial infectious diseases, eye diseases, and sarcoidosis. It also serves as a biomarker for toxic shock syndrome.

Detailed Function and Structure

The HLA-DRB1 gene encodes a protein essential to the immune system. It is part of the human leukocyte antigen (HLA) complex, which helps the immune system differentiate between the body’s proteins and those of foreign invaders, such as viruses and bacteria. The HLA complex is the human equivalent of the major histocompatibility complex (MHC) found in many species. HLA-DRB1 belongs to the MHC class II group, which encodes cell-surface proteins. These proteins bind to extracellular peptides and display them to the immune system, prompting a response if they are identified as foreign.

The beta chain produced by HLA-DRB1 binds to the alpha chain produced by HLA-DRA, forming the HLA-DR antigen-binding heterodimer. This complex displays foreign peptides to the immune system, triggering an immune response. Each MHC class II gene has numerous variations, enabling the immune system to respond to various foreign invaders. Researchers have identified hundreds of HLA-DRB1 alleles, each designated by a unique number (e.g., HLA-DRB1*04:01).

Allele DRB1*01:01 #

Bacillus anthracis pagA/protective antigen, PA: KLPLYISNPNYKVNVYAVT

HIV-1 gag peptide: FRDYVDRFYKTLRAEQASQE

VP1: PRFSLPFLSIASAYYMFYDG

VP2: PHQFINLRSNNSATLIVPYV

PKYVKQNTLKLAT

SNGNFIAPEYAYKIVK

M-derived epitope: GLIYNRMGAVTTEV

COL4A3: GWISLWKGFSF

MBP: VHFFKNIVTPRTP

Allele DRB1*03:01 #

HRV-16 capsid protein VP2: NEKQPSDDNWLNFDGTLLGN

Retinal SAG: NRERRGIALDGKIKHE

Thyroid TG: LSSVVVDPSIRHFDV

HHV-6B gH/U48 and U85 antigens (no specific peptide sequences provided)

C. tetani neurotoxin tetX (no specific peptide sequences provided)

Allele DRB1*04:01 #

M. tuberculosis esxB/culture filtrate antigen CFP-10: EISTNIRQAGVQYSR

QNILLSNAPLGPQFP

DYSYLQDSDPDSFQD

GVYATR/citSSAVR

SAVRAR/citSSVPGVR

ACAN: VVLLVATEGR/CitVRVNSAYQDK

COL2A1 (no specific peptide sequences provided)

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VIM: Native or citrullinated self-peptides (no specific sequences provided)

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VP1: HIVMQYMYVPPGAPIPTTRN

VP2: RGDSTITSQDVANAVVGYGV

VIM: SAVRAR/citSSVPGVR

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Tumor-associated antigen WT1: KRYFKLSHLQMHSRKH

Allele DRB1*05:01 #

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EBV latent antigen EBNA2 peptide: PRSPTVFYNIPPMPLPPSQL

VP2: VPYVNAVPMDSMVRHNNWSL

Tumor-associated antigen WT1: MTEYKLVVVGAVGVGKSALTIQLI

KRAS neoantigen: MTEYKLVVVGAVGVGKSALTIQLI (G12V mutation)

Allele DRB1*11:01 #

HRV-16 capsid protein VP2: SDRIIQITRGDSTITSQDVA

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HHV-6B antigens (no specific peptide sequences provided)

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HRV-16 capsid protein VP2: SNNSATLIVPYVNAVPMDSM

MBP: ENPVVHFFKNIVTPR

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Research context

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Live-Cell Imaging and Internalization Studies

FAM-labeled peptides are indispensable tools for tracking cellular uptake and intracellular trafficking. For example, FAM-conjugated ovalbumin peptide (Fam-ova, SIINFEKL) has been widely used to study MHC-I antigen presentation and visualize cytosolic antigen release via confocal microscopy. Similarly, FAM-labeled cell-penetrating peptides (e.g., TAT-derived conjugates) have enabled real-time monitoring of peptide internalization.

Source: lifetein.com ↗

Clinical Trials and Research

Several clinical trials have explored the use of PADRE in cancer vaccines. For instance, vaccines targeting Mucin 1 (MUC1), a glycoprotein overexpressed in many cancers, have shown promising results when combined with PADRE. These vaccines have demonstrated the ability to elicit strong immune responses, including the production of antibodies against cancer-specific antigens.

Source: lifetein.com ↗
Practical and safety references

These excerpts are educational, not personalised medical instructions.

Storage reference

Storage Conditions

Store labeled peptides in opaque vials at -20°C to prevent photodegradation. Avoid repeated freeze-thaw cycles.

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Potential benefits

What are the benefits of lipidating my peptide?

Lipidation can alter peptide solubility and enhance stability, cellular uptake, and membrane interaction, making it beneficial for various applications, including therapeutics and drug delivery.

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Peptide Therapy Guide Editorial Team

Editorial team for Peptide Therapy Guide.

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