Immunoglobulins (antibodies) are the glycoproteins involved in the immune response. Immunoglobulins recognize and bind antigens and can be found in the plasma linked to lymphocyte cellular membranes. The molecule is comprised of two identical s.c. light chains and two heavy chains that are linked by disulphide bridges [1]. The characteristic feature of antibodies is the highly variable sequence pattern, which recognizes and specifically binds to the exposed antigen. This feature of antibodies allows the immune system to react to a broad range of allogenic agents.

Variable regions are located at the N-terminal region of the heavy (VH) and light (VL) chains. Together with the two other constant regions of the heavy and light chains, CH1 and CL, respectively, these regions form one of two Fab fragments (antigen binding fragment). The third component of the molecule is called the Fc-fragment (crystallizable fragment) and is comprised of the invariable CH2 and CH3 domains of the heavy chains. This latter portion of the antibody is involved in interaction with the cell surface, the complement system, and in antibody transportation [2]. Immunoglobulins are separated into 5 subclasses, IgG, IgA, IgM, IgD and IgE. The classes are distinguished by their localization, prevalence, role and participation in the immune response. In addition, immunoglobulins differ in their structure and shape, especially in the non-variable portion of the antibody [3]. IgGs, the most common human immunoglobulins, represent 75% of all plasma immunoglobulins and have several functions including triggering the complement system (the proteolytic plasma enzyme cascade involved in antigen degradation in the blood). Members of the IgG class of immunoglobulins can be subdivided according to their biochemical features, which include their affinity for complement system proteins and their concentration in the plasma [4]. Structurally, IgGs differ most in the hinge area (the section between the Fab and Fc fragments) [5]. The model presented provides a view of the common IgG1 protein. Light chains are shown in red, heavy chains are in grey, disulphide bridges linking the chains are in yellow, and the oligosaccharide is in dark grey.


Wiley, Monash University (Australia)

Date: Apr 21, 2014


I would like to express my gratitude to Visual Science and all its employees who participated in the Second Nanotechnology International Forum organization. Thank you for your professionalism and the high quality product
A.B. Chubais, CEO of SC "Rusnanotech" RUSNANO
Project Inquiry

Tell us how to reach you and we’ll contact you shortly

Your request was sent. Thank you for your interest!